NZ754916B2 - Volatile organic compound formulations having antimicrobial activity - Google Patents

Abstract

The present invention includes chemical formulations with an antimicrobial component comprising propanoic acid and/or isobutyric acid and isoamyl hexanoate. Methods of treating a microbial infection, disease, or disorder (such as calf scours) with said formulations are also disclosed, as are methods of treating human or animal waste (including in litter boxes), and methods of sterilizing surfaces. of treating human or animal waste (including in litter boxes), and methods of sterilizing surfaces.

Description

LE ORGANIC COMPOUND FORMULATIONS HAVING ANTIMICROBIAL ACTIVITY CROSS-REFERENCE TO RELATED APPLICATIONS The present application claims priority to US. Provisional Application No. 61/842,362, filed July 2, 2013, and US. ional ation No. 61/948,902, filed March 6, 2014, each of which applications are incorporated by nce herein in their entireties.

BACKGROUND OF THE INVENTION The importance of safely disposing billions of pounds of human and animal excrement each day so as to avoid the myriad of health problems associated with such wastes cannot be overstated. In reality, only a fraction of this massive amount of material is safely treated, while the remainder is untreated and poses a threat to human and animal health. For instance, it is well known that the complex of ial and other agents causing gastrointestinal diseases is the world’s largest single cause of mortality. It is also well known that these types of diseases impact primarily infants and children, as well as livestock. It is estimated that over the next ten years, at least twenty million people will die as a result of poor or inadequate sanitation facilities.

One of the reasons for this is that approximately 2.4 billion people live in areas without adequate sanitation facilities. Nearly 4000 children die each day from conditions such as diarrhea. In addition, people suffering from water-bome es occupy about half of the s hospital beds. In several c countries, twice as many people are dying from ea-related es as from AIDS. Essentially, the poor sanitation conditions are resulting from or related to the inability of homes, communities and in some instances, entire countries, to adequately treat and dispose of human and animal wastes, which bear and promote the growth and development of disease-causing microorganisms.

Without on, the unwanted effects of microorganisms in industrial gs are numerous. For example, safer and more effective means for treating microbe-laden surfaces in medical or hospital environments are needed. Safer and more effective means for treating agricultural crops for unwanted microbial grth are needed. Further, a means for reducing the ed odors produced in the breakdown of fecal matter in industrial farming operations is desperately needed.

There is an urgent need for the replacement of antibiotics with other types of compounds that also exhibit antimicrobial activity. Continued use of most of the commonly used antibiotics for animals and agriculture has ed in acquired resistance in microbial populations, especially microbes that are capable of being pathogenic. Every year, at least 23,000 people in the United States die due to infections caused by drug resistant bacteria, and the number is increasing.

Thus, there is a need in the art for antimicrobial compositions suitable for reducing rganisms and the effects of microbial outgrowth in a wide range of industrial settings, as well as for formulas and methods of human and animal waste treatment. The present invention es this need.

BRIEF SUMMARY OF THE INVENTION In one ment, the t invention relates to a al formulation having crobial activity comprising propanoic acid, isobutyric acid, and at least one ester. In another embodiment, the at least one ester is isoamyl hexanoates. In another embodiment, the formulation further includes at least one carrier selected from the group consisting of bentonite, e and perlite. In another embodiment, the ratio of propanoic acid: ryic acid: isoamyl hexanoates is about 3.5:3.5:2 v/v/v. In another embodiment, the ratio of propanoic acid, isobutryic acid and isoamyl hexanoates is about 7 parts of the two acids and 2 parts of isoamyl butyrate. In another embodiment, the formulation further includes at least one endophyte. In another embodiment, the endophyte is of the genus 'um.

In r embodiment, the present invention relates to a chemical ation consisting essentially of propanoic acid, isobutryic acid, isoamyl hexanoates and a carrier selected from the group consisting of bentonite, zeolite and perlite.

In another embodiment, the present invention relates to a al formulation comprising propanoic acid and at least one 6-12 carbon (acid) component ester, wherein the chemical formulation has a ratio of propanoic acid:ester component of about 7:2 v/v. In another embodiment, the at least one ester is l hexanoates. In another embodiment, the formulation further includes at least one nutritional supplement and at least one salt. In another embodiment, formulation ses glucose, whey protein, potassium chloride, magnesium sulfate, and sodium chloride. In another embodiment, the formulation comprises glucose, WO 03082 e, potassium chloride, sodium chloride, and magnesium acetate. In another embodiment, the ation comprises glucose, glycine, potassium chloride, sodium chloride, magnesium acetate, and monopotassium phosphate. In another embodiment, the formulation further includes at least one carrier. In r embodiment, the ation consists essentially of propanoic acid and isoamyl hexanoates at a ratio of propanoic acid:isoamyl hexanoates of about 7:2 V/V. In another ment, the formulation includes at least one endophyte. In another embodiment, the endophyte is of the genus Fusarz'um.

In another embodiment, the present invention relates to a method of treating an animal haVing a disease or disorder associated with a microbial ion, comprising administering to the animal an effective amount of a composition comprising at least one organic acid and at least one ester. In another embodiment, the present invention relates to a composition comprising propanoic acid and at least one 6-12 carbon (acid) component ester, wherein the chemical formulation has a ratio of propanoic acid:ester component of about 7:2 V/V.

BRIEF DESCRIPTION OF THE DRAWINGS The following detailed description of embodiments of the ion will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the ion is not limited to the precise arrangements and instrumentalities of the embodiments shown in the drawings.

Figures 1 rates a plate bioassay to determine the bioactiVity of various esters when combined with a 1:1 mix of the two organic acids as per Table 2. The test organisms were as follows- Cercospora (dark-lower left bottom) then clockwise — Phytophthora, Verticillium, tinia, Pythium. Fusarium, Trichoderma, Rhizoctonia, and Aspergillus. The streaks were Saccharomyces (far right ) then Candida, E coli and Bacillus (left bottom). A = control plate, and B = plate with System 1 after incubation for 30 hr.

Figure 2 rates the effects of System 1 on the growth of bacteria from human wastes.

About 5 mg of fresh human waste was spread over the surface of a Petri plate with potato dextrose agar. Then plugs were d from the center and bentonite was placed in the well ca. 0.5 g. The bentonite in the center well did not have the ingredients in System 1 on it (center) but the well on the far right had System 1 at the rate of 1 ml System 1 per 10 g of bentonite. The plates were incubated for 48 hr at 22 °C and then photographed. There was no detectable bacterial growth in the System 1 treated plate, but the control plates had ample bacterial colonies.

Figure 3 illustrates the s of System 2 on the growth of bacteria from human wastes.

About 5 mg of fresh human waste was spread over the e of a Petri plate with potato dextrose agar. Plugs were removed from the center and bentonite was placed in the well ca. 0.5 g. The bentonite in the center well did not have the ingredients in System 1 on it (center) but the well on the far right had system 1 at the rate of 1 ml System 1 per 10 g of bentonite. The plates were incubated for 48 hr at 22 °C and then photographed. There was no detectable bacterial growth in the System 2 d plate.

Figure 4 illustrates two cat litter boxes with cat fecal matter each from 5 ent cats ca. 140 g. The box on the right had been treated with System 1 on bentonite with (0.5 ml / 100 g bentonite). After 5 days the ammonia readings were 14 ppm on the control (left) and 0 ppm on the treated right. The l odor was significantly reduced in the treated box.

Figure 5 illustrates treatment of ca. 140 g of human waste in the presence of urine with Fusarz'um subglutinans 06-1 in the presence of System 2 (1 ml on 10 g of zeolite). After 3 weeks there was substantial grth of the F. subglutinans (white um in the right container). The ammonia level was 71.4 in the l on the left and 12.1 in the treated container on the right.

No fungal growth and no degradation of the wastes occurred in the control (left).

Figure 6 illustrates the progressive growth ofFusarz'um spp on small dollops of human waste ca. 100 mg (fresh weight) over the course ofmany days. The growth of newly isolated and characterized 'um spp. are each compared to P2-24 (Fusarl'um culmorum). The new Fusarz'um spp. especially E06-l and E06-5 do grow faster on the waste. Growth was measured from the extent of the mycelium moving out from the agar plug placed on the dollop of waste.

Figure 7 illustrates a six day old culture ofFusarl'um subglutinans E06-l (top) the red fungus to be used to treat human and animal wastes in combination with System 2. A light microscopic view of spores and hyphae of F. subglutinans is also shown (bottom). The spores are slightly curved and are 9.8 -12 x 2.5 u.

Figure 8 illustrates Fusarz'um subglutinans (E06-8) growing profusely on human waste (center) in the presence of System 2 with bentonite as the carrier. Please note the inhibition of bacterial growth to the left and center of the culture plate which is influenced by the vapors of System 2 emanating from the ite particles on the left side of the plate allowing for fungal growth. There were 0.5 g of treated bentonite added, ca 100 mg of human waste and the plate had incubated for 12 days. See Figure 6 for ative growth measurements.

Figure 9 depicts the biological ties of various test mixtures against a panel of test microbes. A small plug of each organism was placed in the periphery of the PDA plate. In the center well was placed the test solution in the plastic cup holder. A control plate (A) was also set up. After 30 hr the growth of the test organisms was compared to that of the control and the % inhibition was calculated. The (B) plate contained the test e. Measurements were made 30 hr after plate set up.

Figure 10 depicts the reduction of microbial contamination of cracked corn via a 1 hr treatment with various concentrations of the S-3 solution. Concentrations above 0.5% totally reduced bacterial ination as seen by the lack of bacterial colonies in the 0.5% and 1.0 % treatments (above). Some minimal fungal contamination was observed in the latter- notice two fungal colonies in each of the plates on the right. Incubation was for two days at room temp and then photographed.

Figure 11 depicts the use of bentonite with various (S) formulae treatments over the course of 3 days to kill E. coli in human wastes (mid plate streak) while allowing for the growth of um (top of plate) that would otherwise breakdown and consume the solid matter in human waste.

Figure 12 depicts the effectiveness of the S-3 formula in treating the fecal matter of chickens made up by first spreading a sion on plates of PDA and then adding 0.5 g of zeolite treated with 3ml per lb (0.45 kg) of S-3. The photo was taken after 3 days of incubation at room temp. It can be seen that the plate containing the S-3 zeolite was virtually free of bacterial contamination.

Figure 13 depicts 1 ft.2 (0.09 m2) plastic snap-seal-top containers filled with litter treatment plus untreated bentonite in the proportions indicated by the packaging instructions to e efficacy of the (S) formulae.

Figure 14 depicts the average ammonia levels taken over 5-minute intervals every 24 hours (A). The peak a levels displayed a similar trend, with S-1 treated litter showing significantly reduced a production levels (B). Figure 14B also depicts peak a levels taken from 5-minute interval tests every 24 hours.

Figure 15 depicts the microbiological activity of S-1 verses a control sample. Figures 15A and 15B indicate that the bentonite control (15A) had massive amounts of bacterial colonies growing all over the plate, ing in those areas close to the well ning the litter. In contrast, the S-1 treatment (4 ml S3 per pound (0.45 kg) of carrier, 15B) was virtually free of ial colonies around the well of the plate.

Figure 16 depicts 1 ft.2 (0.09 m2) plastic snap-seal-top ners filled with pine gs and the desired bedding treatment, in the proportions indicated by the packaging instructions. For these tests, S-1 applied at the rate of 15 ml per lb (0.45 kg) of zeolite and an untreated zeolite control were tested.

Figure 17A depicts the average ammonia levels taken over 5-minute intervals every 24 hours. The peak ammonia levels displayed a similar trend, with rd Bedding-treated bedding showing the lowest a tion levels (Figure 17B). Figure 17B depicts the peak ammonia levels taken from 5-minute interval tests every 24 hours.

Figure 18 depicts 1 ft.2 (0.09 m2) plastic snap-seal-top container filled with pine shavings (a commonly used bedding material for large animals) and the desired bedding treatment, in the proportions indicated by the ing instructions. For these tests, S-1 treated, and an untreated zeolite control were tested.

Figure 19 depicts the average ammonia levels taken over 5-minute intervals every 24 hours (19A). The peak ammonia levels displayed a similar trend, S-1 treated bedding showing the lowest ammonia production levels (19B). Figure 19B depicts peak ammonia levels taken from 5-minute interval tests every 24 hours.

Figure 20 s a scoured calf prior to any treatment with S-X solution (Figure 20A), and after two rounds of treatment with S-X solution (Figure 20B).

Figure 21 depicts a scoured calf prior to any treatment with S-X solution (Figure 21A), and 24 hours after treatment with S-X solution (Figure 21B).

Figure 22 is an image ing dairy cow conditions at Dairy 1.

Figure 23 depicts the typical creamy yellow scours exhibited on calf 919 (Figure 23A), and calf 919 fully recovered after treatment with S-X on (Figure 23B).

Figure 24 depicts calf 166 of Ranch 9 suffering with scours in the winter of 2014 (Figure 24A) and one day after treatment with S-X on (Figure 24B), wherein the animal recovered and yellow diarrhea subsided.

Figure 25 depicts a sheep suffering from mastitis (Figure 25A) and administration of the S-3 formula to the animal via syringe (Figure 25B).

Figure 26 depicts raspberries d with control bentonite in the center well (Figure 26A) and those treated with the S-3 1:10 mixture (Figure 26B) and stored for 1 week at room temperature. The berries treated with S-3 were edible and had no decay.

Figure 27, comprising Figures 27A-27B, depicts soil treated with P. ultimatum or S-3.

Figure 27A is a photograph of soil treated with P. ultimatum alone with seeds of red beet. Only one or two seeds were observed to germinate. Figure 27B is a photograph of soil treated with S-3 on bentonite in the presence of P. ultimatum and red beet seeds. Many of the seeds were ed to germinate.

Figure 28, comprising s 28A-28D, depicts images of water agar plates for testing of S-3 with red beet seed. Figure 28A is an image of an agar plate with red beet seed, bentonite, S-3 (1 part to 10 g bentonite), and P. ultimum. S-3 was found to control the growth of P. ultimum. Figure 28B is an image of an agar plate with red beet seed and P. m. Figure 28C is an image of an agar plate with red beet seed alone. Figure 28D is an image of an agar plate demonstrating that S-3 was not harmful to the red beet seed.

DETAILED DESCRIPTION It is to be tood that the figures and descriptions of the present invention have been simplified to illustrate elements that are nt for a clear understanding of the present invention, while eliminating, for the purpose of clarity, many other elements found in typical antimicrobial formulations. Those of ordinary skill in the art may recognize that other ts and/or steps are desirable and/or required in implementing the present invention. However, because such elements and steps are well known in the art, and e they do not facilitate a better understanding of the present invention, a discussion of such ts and steps is not provided herein. The disclosure herein is directed to all such variations and modifications to such elements and methods known to those skilled in the art.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly tood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials r or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred s and materials are bed.

As used herein, each of the ing terms has the g associated With it in this section.

The articles “a” and “an” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.

“About” as used herein When referring to a measurable value such as an amount, a temporal duration, and the like, is meant to encompass variations of 20%, 10%, 5%, l%, and ::0. 1% from the specified value, as such variations are appropriate.

“S-l” as used herein refers to any and all formulations of System 1.

“S-2” as used herein refers to any and all formulations of System 2.

“S-3” as used herein refers to any and all formulations of System 3.

“S-4” as used herein refers to any and all formulations of System 4.

“S-5” as used herein refers to any and all formulations of System 5.

“S-X” as used herein refers to any and all formulations of System X, Which may include one or more of Systems 1-5 therein.

As used herein, the term “CLOE” refers to a formulation comprising S-1 or S-5.

As used herein, the term “Barnyard g” refers to a ation comprising S-1 or S-5.

As used herein, the term “pharmaceutical composition” refers to a mixture of at least one composition of the invention With other chemical components, such as rs, izers, diluents, dispersing agents, suspending agents, thickening agents, and/or excipients. The pharmaceutical composition facilitates stration of the composition to an organism.

Multiple techniques of administering a composition exist in the art including, but not limited to, intravenous, oral, aerosol, parenteral, ophthalmic, pulmonary and topical administration.

As used herein, the term “pharmaceutically acceptable” refers to a material, such as a carrier or diluent, Which does not abrogate the biological activity or ties of the composition, and is relatively xic, i.e., the material may be administered to an individual Without causing undesirable biological effects or interacting in a deleterious manner With any of the components of the composition in Which it is contained.

As used herein, the term “pharmaceutically able carrier” means a pharmaceutically acceptable material, composition or carrier, such as a liquid or solid filler, stabilizer, sing agent, suspending agent, diluent, ent, thickening agent, solvent or encapsulating al, ed in carrying or transporting a composition useful within the invention within or to the patient such that it may perform its intended function. Typically, such constructs are carried or transported from one organ, or portion of the body, to another organ, or portion of the body.

Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation, including the composition useful within the invention, and not injurious to the patient. Some examples of materials that may serve as pharmaceutically acceptable carriers include: sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato ; cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl ose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients, such as cocoa butter and suppository waxes; oils, such as peanut oil, cottonseed oil, er oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene ; polyols, such as in, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate; agar; buffering agents, such as magnesium hydroxide and aluminum hydroxide; surface active agents; alginic acid; pyrogen-free water; isotonic saline; Ringer’s solution; ethyl alcohol; phosphate buffer solutions; and other non-toxic compatible substances employed in pharmaceutical formulations.

As used herein, “pharmaceutically acceptable carrier” also includes any and all coatings, cterial and antifungal , and absorption delaying agents, and the like that are ible with the actiVity of the composition useful within the invention, and are physiologically acceptable to the patient. Supplementary active compositions may also be incorporated into the compositions. The aceutically acceptable carrier” may further include a pharmaceutically acceptable salt of the composition useful within the invention. Other additional ingredients that may be included in the pharmaceutical compositions used in the practice of the invention are known in the art and bed, for example in Remington's Pharmaceutical Sciences (Genaro, Ed., Mack hing Co., 1985, Easton, PA), which is incorporated herein by reference.

Throughout this disclosure, various aspects of the invention can be presented in a range format. It should be understood that the description in range format is merely for ience and breVity and should not be construed as an inflexible limitation on the scope of the invention.

Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed ges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual s within that range, for example, 1, 2, 2.7, 3, 4, 5, 5.3, 6 and any whole and partial increments therebetween. This s regardless of the breadth of the range.

The present ion relates to the discovery of effective and useful chemical formulae that, either alone or in combination with certain endophytic fungi, such as Fusarl'um spp, have strong antimicrobial ty and may be particularly suitable for a variety of uses, such as to reduce ial growth from medical facility surfaces or instruments, reduce ial growth on agricultural plant surfaces, or to decontaminate, degrade and deodorize human and animal wastes. For example, the formulae of the present invention are suitable for the treatment of wastes in any location, such as in latrines, cat litter boxes, animal stalls, barns, chicken raising facilities, pig barns, pet stations in homes, zoos and a host of other locations.

In a preferred embodiment, the appropriate combination of the harmless formulae containing ingredients that are on the FDA- GRAS list and an riate fungi, such as an endophytic fungi Fusarz'um spp, such as F. subglutz‘nans, are placed together into a container, such as a biodegradable plastic bag. Also contained in the bag is an appropriate amount of a absorbing polymer that is compatible with the endophytic Fusarz'um subglutinans. This combination of agents represents a safe, rapid and novel treatment process for the recycling of ingredients found in human and animal wastes. The presence of these two ingredients in the bag effectively kills many of the harmful ia in the human wastes and at the same time begins the process of recycling the c consteatuents of the wastes back to a harmless soil additive.

The present invention can be employed in connection with such activities as national emergencies, military maneuvers, marine-related activities, natural disasters, outdoor sporting activities (camping, hiking, canoeing, hunting, , etc.) and other activities in which human wastes need to be properly and safely disposed. It also relates to the development ofmuch safer facilities for all livestock and even household pets. As an example, it has been recently noted that proper and safe disposal of human waste is an important concern for the appropriate management of wildland areas of the world. Aesthetics, as well as health concerns, are the major issues facing 2014/045297 managers of these areas. Accordingly, the present invention may be suitable for human and animal surfaces, plant surfaces, industrial es, machine tools and a host of other uses.

In one embodiment of the present invention, the formulations of System 1 (S-l), System 2 (S-2), System 3 (S-3), System 4 (S-4) and/or System 5 (S-S), and optionally using bentonite, zeolite or perlite as a carrier ding on application), are combined together in the container and the processes of bacterial killing and/or waste degradation begin immediately. In another embodiment, the present invention may be used in animal bedding and stall treatments, wherein the chemical mixture (with the carrier) can be applied directly to the areas housing the animals, resulting in the almost immediate killing of bacteria that cause harmful odors such as ammonia.

In r embodiment, the present invention may be applied to a surface, such as an agricultural plant surface, a medical facility surface, a medical or rial tool, or the like, to ate or otherwise reduce the microbial count on the treated surface.

Antibiotics are compounds that either kill or inhibit the growth of bacteria. A frequent misconception is that antibiotics are effective against other rganisms, such as fungi and Viruses, when in fact antifungal and antiviral compounds are needed for such purposes.

Antibiotics work by interfering with key steps in the metabolism and growth of bacteria and can be broadly d into two main categories, bacteriosides and bacteriostatics, depending on whether they kill bacteria or simply inhibit their growth, respectively. Antibiotics are generally safe for use in humans because the steps they target are either unique to certain types of bacteria or are effective against bacteria at very low concentrations considered safe for humans. Other classes of als, such as certain alcohols, acids, and des may have broad inhibitory and/or killing power because they affect fundamental elements of mistry common to many forms of life. These kinds of compounds are classified as antiseptics, sterilants, disinfectants, and sanitizers, and preservatives ing on their specific effects on ial life, modes of effective application, and ty to humans. The systems of the present invention, such as S1, are mixtures consisting primarily of short chain organic acids and esters, mostly notably propanoic acid and isoamyl hexanoates. Neither of these molecules is classified as an antibiotic, but both possess antimicrobial properties and can be either bactericidal or bacteriostatic depending on the concentration and length of application.

The systems of the present ion do not work by the same mechanisms as antibiotics.

Whereas otics target very specific steps, often by recognizing very specific structural motifs, the s of the present invention kill bacteria and inhibit their growth by effecting fundamental biochemical properties ed to sustain life. Moreover, the components of the systems of the present invention act synergistically such that the effect of the overall mixture is greater than sum of its parts. The mechanism of the istic effect seen with these systems is not understood, but other acid/ester mixtures display the same sort of exaggerated combined effect.

One major component of the systems of the present invention, propanoic acid, is a short chain organic acid with an established use as a preservative in the food and agricultural industries. Most organisms, including humans and many bacterial species, have metabolic pathways that facilitate the use of propanoic acid as nutrient and in fact, one group of bacteria can even e the molecule. Thus, at low concentrations propanoic acid is essentially harmless to almost all organisms, but at higher concentrations it cannot be degraded fast enough and begins to accumulate within the cell. As its concentration within the cell increases, so too does the acidity of the cell. When the acidity inside the cell is too high, s cannot function properly, DNA and other biological molecules are destroyed, and the cell dies. Recent studies indicate that although effects on intracellular acidity are a major crobial mechanism of weak organic acids, it is by no means the only mechanism. As acids dissociate and release protons inside the cell, they become negatively charged. High concentrations of negatively charged molecules inside the cell present a host of detrimental effects on osmolarity, nt e, and metabolism.

At lower concentrations acids may be inhibitory, but not lethal. Increases in acidity occur when an acid dissociates and releases a proton. When the y inside a cell s too great, the cell can export protons to the outside in an attempt to maintain proper pH levels. Although effective, this strategy requires the consumption of a large amount of energy and can occur without ity only at low acid concentrations. Because smaller organisms are more sensitive to smaller amounts of propanoic acid, a concentration that is harmless to humans may be fatal or inhibitory to bacteria. Propanoic acid is not the only organic acid in S l , but the antimicrobial effects of other similarly sized organic acids can be presumed to arise from essentially the same ism.

The antimicrobial mechanism of esters remains y n. Although not wishing to be bound by any particular theory, one possible clue comes from the observation that for a WO 03082 given set of esters, those that are able to orate more effectively into the bacterial cell membrane tend to have increased antimicrobial properties. Incorporation of any molecule into the cell membrane changes the chemical and physical ties of the membrane, which leads to changes in nutrient uptake, waste export, energy generation, and other essential ar processes. Although not wishing to be bound by any particular theory, this observation has led to the suggestion that incorporation of n esters into the cell membrane changes its chemical and al properties in a way that is detrimental to the sm. Alteration of the cell membrane is also a mechanism by which longer chain organic acids are thought to work.

As antibiotics began to be applied on a massive scale during the 20th century, the problem of antibiotic resistance emerged as a major clinical issue. In the 21St century, as the consequences of antibiotic resistance became more Visible and widespread, the term entered the public consciousness and was finally recognized for the immense problem that it is. In a bacterial population exposed to antibiotics, resistance is either existent in a very small number of individuals or initially emerges because of natural ons and is subsequently selected for because indiViduals resistant to the antibiotic have a al advantage over non-resistant individuals. Antibiotic resistance spreads by both vertical transmission from a resistant cell to its progeny and by horizontal transmission (direct transfer of ance genes from a resistant cell to a non-resistant cell). In this way, resistance spreads rapidly and sed antibiotic usage consteatutes a selective pressure that increases the survival advantage of antibiotic resistance.

Bacteria can acquire resistance to a given otic Via four primary mechanisms: evolving s that inactive the antibiotic, altering the structure of the target so the antibiotic can no longer bind, rerouting metabolic pathways to skip antibiotic inhibited steps, and developing efflux pumps that pump the antibiotic outside the cell. Each mechanism has a genetic basis and can thus be transferred from the cell that initially ped resistance to non-resistant cells. In some cases, a bacterial cell can acquire resistance to several ent kinds of antibiotics. This is how so called “super-bugs” arise and as the usage of antibiotics increases in the agricultural, veterinary, and medical industries, so too will the prevalence of multi-drug resistant bacterial strains. In addition, combinations of small organic molecules, such as acids and esters, that act in a synergistic manner to yield Virtually the same antimicrobial effect as antibiotics have been fied. Organic molecules that possess these properties may be referred to as “synergistans.” The mechanisms of antibiotics, as well as resistance to them, can be summed up by one word — specificity. Antibiotics work by targeting specific structural es, enzymes, and olecules. Likewise, antibiotic resistance occurs when bacteria develop an efflux pump specific for a given otic or alter a particular structural feature, enzyme, or macromolecule.

If antibiotics are specific, the components of the s of the present invention are general.

Organic acids and esters lack specific targets, instead they exert their antimicrobial effects by changing the biochemical environment of bacterial cells. They are effective against a much wider range of organisms and they interfere with multiple cellular processes.

Organic acids are abundant in nature. Any given bacterial cell will invariably be exposed to organic acids at some point in its lifetime and as a result, many bacterial species s innate genetic mechanisms that, upon induction, help them cope with the stresses brought about by natural organic acid exposure. s the best studied of these is the ella acid tolerance response. Essentially when a salmonella cell is exposed to a high, but sub-lethal acid concentration, it induces the expression of a number of genes such that the next time it is exposed to acidic conditions, its chances for survival are much greater. This has been trated experimentally by ating an acidic medium with previously exposed and unexposed salmonella cells. In almost every case, the previously exposed cells are afforded a much higher tolerance to the acid. E. 0012' also has a thoroughly studied acid nce response and it seems likely that the mechanism is t in many other bacterial species. In the case of pathogenic species like Ecolz' and salmonella, there is great concern that induction of the acid tolerance response by exposure to sub-lethal concentrations of organic acid food vatives could increase bacterial virulence e the bacteria are more likely to survive exposure to acidic c fluids during digestion.

Nevertheless, there is an important difference between resistance to antibiotics and resistance to c acids. Many of the genes for antibiotic resistance lie on mobile c elements known as plasmids that are easily transferred between bacterial cells and bacterial species. In this way, it is a relatively simple process for any given bacterial cell to acquire resistance to numerous antibiotics. Acid resistance mechanisms such as the acid tolerance response, on the other hand, are encoded on chromosomal DNA. This kind of genetic information can only be transferred to progeny cells and thus the sudden rise of “super-bugs,” as has been observed with multi-drug resistance bacterial strains, does not apply. Moreover, although not wishing to be bound by any particular theory, it is possible that the synergistic effects observed when an organic acid is used in conjunction with c esters could negate some acid resistance mechanisms.

In one embodiment, to identify a microbe that could grow on human and animal wastes resulting in their degradation, it was essential to formulate a novel antibiotic mixture that would kill the ial contents of the wastes that normally act to break down urea to a and uric acid. The ammonia is lethal to most fungi that otherwise would degrade the solid constituents of the wastes. Central to this ery is the known fact that propanoic acid has antibacterial activities but only at the inhibitory level, and the same is true for ryic acid.

Thus, these two nds were the starting ingredients for the new and effective antibiotic mixture. What was needed was an additional ingredient to lend microbial lethality to the mix.

Then, in a completely unexpected manner it was learned that the addition of certain esters to these small organic acids would lend to them significantly enhanced antimicrobial activities.

Microorganisms living in the world’s rainforests, in order to survive, must have d biochemical mechanisms to cope with potential competitors. In this regard, they developed an ability to produce molecules that are antimicrobial and compounds that inhibit and destroy other es. Because new antibiotics are sought after by mankind, researchers visit rainforests in search of new microbes and the agents that they produce to inhibit and destroy other microbial competitors. Certain rest microbes have provided important chemical clues as to which compounds have been chosen for Systems 1-4.

Formulations In part, the present invention includes a al formulation comprising at least one organic acid, such as oic acid, isobutyric acid, or butyric acid. In one embodiment, the chemical formulation has antibacterial activity when applied to human or animal waste. In certain embodiments of, the organic acid that is used may n from 2—5 carbon atoms and each acid used can vary from 0% to 80% of the bioactive mixture. In a preferred embodiment, the organic acid is propanoic acid. In another embodiment, the t invention includes a chemical formulation consisting essentially of an c acid, such as oic acid, isobutyric acid, or butyric acid. In one embodiment, the chemical formulation consists essentially of propanoic acid. In certain embodiments, the chemical formulation comprises two organic acids.

In one embodiment, the two organic acids are propanoic acid and isobutyric acid. In one embodiment, the chemical formulation comprises a ation of two organic acids and at least one ester. In one embodiment, the chemical formulation comprises propanoic acid, isobutryic acid, and at least one ester. In another embodiment, the two organic acids are propanoic acid and isobutyric acid and the at least one ester is isoamyl butyrate. In another embodiment, the two organic acids are propanoic acid and isobutyric acid and the at least one ester is isoamyl hexanoates. In another embodiment, the two organic acids are propanoic acid and isobutyric acid and the at least one ester is isoamyl acetate.

As contemplated herein, the chemical formulation may further comprise at least one ester. As contemplated herein, the at least one ester may be any ester listed in Table l or elsewhere herein. In certain embodiments, the ester can have from 3 to 10 carbon atoms and any ester or combination thereofmay ent at least 20% of the mixture. In one embodiment, the ester is an isoamyl ester. As contemplated herein, embodiments of the present ion may be atively ated using an entire family of isoamyl esters of various acid components ranging from C-6 (hexanoate) to C-12 (laurate) as well as various aromatic (acid) esters of isoamyl alcohol such as cinnamate, benzoate and, acetate. In one embodiment, the ester is isoamyl hexanoates. As used herein, the term “hexanoates” may mean a single type of hexanoate or may include a mixture of the acid form of hexanoates, including ed forms.

In another embodiment, the ester is isoamyl formate. In another embodiment, the ester is isoamyl butyrate. In another embodiment, the ester is isoamyl acetate. In one ment, the ester is isoamyl acetate. In one embodiment, the ester is selected from the group consisting of allyl acetate, l acetate, isoamyl acetate, and phenethyl acetate. In one embodiment, the ester is strawberry aldehyde (ethyl 3-methylphenyl-oxiranecarboxylate, an c ester).

In certain embodiments, the at least one ester may be any single carbon (acid) component ester.

In one embodiment, the at least one ester is isoamyl formate. In certain ments, other compounds can be added as the ester ent of the formulations. For example, the octanoate ester of isoamyl alcohol is active and so too is the laurate ester. Accordingly, the formulations of the present invention may include use of the entire spectrum from 6-12 carbon (acid) components of the isoamyl esters. In one embodiment, the ester is the ate ester of isoamyl alcohol. In another embodiment, the ester is the laurate ester of l alcohol. In certain ments, benzene components may be used as well as the benzoate ester, the cinnamate, and the salicylate esters. In one embodiment, the chemical formulation comprises propanoic acid and at least one 6-12 carbon (acid) component ester.

In certain ments, the formulae of the present invention may include mixtures of at least one organic acid and at least one ester at any ratio. In one embodiment, the ratio of the at least one organic acid to the at least one ester is about 6-7 to about 2-3. In preferred embodiments, the ratio of the at least one organic acid and the at least one ester is about 7:2. In other embodiments, the formulae of the present invention may include mixtures of two organic acids and at least one ester at any ratio. In one ment, the ratio of a first organic acid: a second organic acid:at least one ester is about 3.5:3.5:2 v/v/v. In another embodiment, the mixture of a first organic acid: a second organic acid:at least one ester is about 7 parts of the two acids and 2 parts of the selected ester. In one embodiment, the chemical formulation comprises propanoic acid and at least one 6-12 carbon (acid) component ester, wherein the chemical formulation has a ratio of propanoic acid:ester component of about 7:2 v/v.

As plated herein, the t invention may include any chemical formulation plus the addition of at least one endophytic fungus. The present invention is not limited to any particular fungus, however and endophytic fungus is preferred, and a fungus from the genus Fusarz'um is more preferred. Most preferred is the endophytic fungus of the species Fusarz'um subglutinans. In another embodiment, the endophytic fungus is a fungus from the genus Gloeosporium. As contemplated herein, the fungus may be incorporated into any ation via inoculated barley, or other suitable carrier for a fungus as is understood by those skilled in the art. In one embodiment, the chemical formulation comprises two c acids and at least one ester and at least one fungus, wherein the two organic acids and the at least one ester kills or reduces bacteria growth on the human or animal waste, and the at least one fungus ses the rate of decomposition of the human or animal waste. In r embodiment, the ation comprises propanoic acid, isobutryic acid, at least one ester and at least one fungus. In certain embodiments, the formulation may additionally comprise cineole, ene, salts or any other additive, excipient or other ent desired to e a ation having the desired characteristic.

In some embodiments, supplementing a fungal culture with onal compounds may enhance its fungal inhibitory properties to an extent greater than either the agents produced by the fungus or the compound alone. Such activity is deemed synergism. Thus, the present invention also provides chemical formulations comprising at least one fungus and at least one synergistan. As used herein, the term “synergistan” refers to any chemical compound that, When administered in combination With another compound, ys r microbial inhibitory actiVity than the actiVity observed When each compound is administered alone. In a non-limiting example, When a istan is combined With a fungal culture, the combined gas phase of the fungus and the synergistans displays increased antimicrobial actiVity than either the gas phase of the fungus or the synergistan alone.

In certain embodiments, the al formulations of the present invention may be used in ation With rs such as zeolite or bentonite as a cat litter treatment, horse barn, cattle barn, sheep barn, or small animal g ent. In such embodiments, the present ion inhibits microbes that inhabit fecal matter, such as E. coli, and break down urea in urine to release ammonia. In another embodiment, the al formulations of the present invention may be added to a carrier such as, Without tion, bentonite, zeolite, perlite or other silica based rs, in amounts that are effective in killing bacteria and reducing harmful and noxious odors.

In certain embodiments, the present invention may be mixed With a foam or other dispersing solution and used as an antimicrobial spray or for es that are contaminated With bacteria or other microbes, such as for the treatment of surfaces in hospitals, home food prep areas, contaminated areas for food processing, including all rial food processors, fruits, meats, and others in Which bacterial contamination is commonly a problem.

In certain embodiments, a composition of the present invention comprises at least one chemical formulation or formula of the present invention. In one embodiment, the compositions of the invention are formulated using one or more pharmaceutically acceptable excipients or carriers. In one embodiment, the pharmaceutical compositions of the invention comprise a therapeutically effective amount of a formula of the invention and a pharmaceutically acceptable carrier. Examples of pharmaceutically acceptable carriers include cremophor, or any other ical surfactant as would be understood by one skilled in the art. In one embodiment, the pharmaceutically acceptable carrier is cremophor.

In certain embodiments, the formulae of the present invention, and preferably S-3, may be used With a carrier (zeolite or bentonite or talc) to treat soil areas that are about to receive either seed or young transplants to reduce or ate damping of infections.

In certain embodiments, the formulae of the t invention may be mixed with detergents to be used as a carpet scrubbing and bacterial decontamination agent for animal waste, human waste or other biofouling of carpet surfaces.

In certain embodiments, the formulae of the present invention may be administered as a spray to decontaminate fruits, vegetables, grains and other agricultural products during planting, during growth, during harvest and/or during transport.

In certain embodiments, the formulae of the present invention may be d to or formulated, embedded or otherwise integrated within baby diapers, bandages or other devices in which bacterial decontamination is desired.

In n embodiments, the formulae of the t invention may be onally formulated with a detergent to function as a soap for the decontamination of human and animal skin.

In certain embodiments, the formulae of the present ion may be onally formulated, embedded or otherwise integrated within a candle wax for area decontamination via vapors when lit.

In particular the chemical formulations of the present invention show remarkable antibiotic activity against bacteria associated with human and animal wastes. These mixture can be cally delivered to their tive target site via inert carriers such as, without limitation, bentonite, e, perlite or other silica based carriers. In this case, the specific on for use of the carrier and the antibiotic combination may include, for example and without limitation, the bedding locations of all domestic and zoo d animals and animals used as old pets. The mixture can be applied to the stalls, g and places where animals live in order to reduce the load of bacteria and harmful gases.

It should be appreciated that the formulations of the present invention may include any additional salts, excipients, nutritional additive or supplement, and the like, such that the final formulation is suitable for topical application, ingestion, inhalation or any other form of administration desired.

System 1 As described elsewhere herein, the chemical formulation may comprise two organic acids and at least one ester. For example, in one embodiment, the formulation includes propanoic acid: isobutryic acid: isoamyl butyrate. In one embodiment, the ratio of propanoic acid: isobutryic acid: isoamyl butyrate is about 5:2 v/v/v. In another embodiment, the mixture of propanoic acid: isobutryic acid: isoamyl butyrate is about 7 parts of the two acids and 2 parts of the selected ester. It should be appreciated that the chemical formulation of System 1 is not limited to any particular ratio of such chemical components. In another embodiment, the al formulation of System 1 consists of only two organic acids and a single ester. In such an embodiment, the formulation consists of oic acid: isobutryic acid: isoamyl butyrate at the ratios described above. In n ments, the formulation may onally comprise cineole, valencene, salts or any other additive, excipient or other component desired to produce a formulation having the desired characteristic.

In another embodiment, the chemical formulation of System 1 may be added to a carrier such as, without limitation, bentonite, zeolite, perlite or other silica based carriers, in s that are effective in killing bacteria and reducing harmful and s odors. This rate is usually 1 ml of System 1 to 224 g of the carrier V/W or in other appropriate ratios that are effective, without tion.

System 2 As contemplated herein, the present invention may include any chemical formulation of System 1 plus the addition of at least one endophytic fungus. As demonstrated herein, endophytic fungi of the group F. subglutinans and others are particularly suited to grow on and degrade human wastes. In addition, the fungus is only able to grow on the liquid and solid waste combination when another antimicrobial mixture such as System 1 is applied and this mixture maximally allows for fungal growth whilst killing bacteria and other es. In one embodiment, the fungus is Fusarz'um subglutinans. In one embodiment, the fungus is orated into System 2 via inoculated barley. In certain embodiments, the formulation may additionally comprise cineole, valencene, salts or any other additive, excipient or other component desired to produce a formulation having the desired characteristic.

In one embodiment, System 2 includes the chemical formulation of System 1, such as propanoic acid: isobutryic acid: isoamyl butyrate in the ratio of 3.5:3.5:2 v/v/v, or 7 parts of the two acids and 2 parts of the ester, which is then added at the rate of l/ 10 V/W of the e to the dry weight of the carrier substance such as ite, perlite or zeolite etc. It should be appreciated that the chemical formulation of System 2 is not limited to any particular ratio of such chemical components. Barley inoculated with Fusarz'um subglutinans is also added. This mixture is then added as 10 g to each container, such as a plastic bag, used to treat and dispose of human wastes. It allows for the rapid growth ofFusarz'um subglutz'nans in contrast to System 1 alone, which does not. Other items may also be added to the bag including liquid absorbing polymers in appropriate amounts, as would be understood by those skilled in the art.

System 3 As contemplated herein, the al formulation of the present invention may se at least one organic acid and at least one ester. In a preferred embodiment, the at least one organic acid is propanoic acid. In one embodiment, the at least one ester is isoamyl hexanoate or a mixture of isoamyl hexanoates. In a red embodiment, the at least one ester is isoamyl hexanoates. In one embodiment, the chemical formulation comprises propanoic acid and isoamyl hexanoates. In certain embodiments, the formulation may additionally comprise cineole, valencene, salts or any other additive, excipient or other component d to produce a formulation haVing the desired characteristic.

In one embodiment, the ratio of propanoic acid: isoamyl hexanoates is about 7:2 V/V. It should be appreciated that the chemical formulation of System 3 is not limited to any particular ratio of such chemical components. In another embodiment, the chemical formulation of System 3 consists of a single organic acid component and a single ester component. In another embodiment, the chemical formulation of System 3 consists of a single c acid ent and a mixture of isoamyl hexanoates. In such an embodiment, the formulation consists of propanoic acid: l ates at the ratios described above. In another embodiment, the chemical ation consists essentially of propanoic acid and isoamyl hexanoates at a ratio of propanoic acid:isoamyl hexanoates of about 7:2 V/V.

In another embodiment, the chemical formulation of System 3 may be added to a carrier such as, t limitation, bentonite, zeolite, perlite or other silica based carriers, in amounts that are ive in g bacteria and reducing harmful and noxious odors.

This rate is usually between 1.0 to 1.5 ml of System 3 to 224 g of the carrier V/W or in other appropriate ratios that are effective, without limitation, such as between 0.1 to 5 ml of System 3 to 224 g of the carrier V/W, or between 0.5 to 2 ml of System 3 to 224 g of the carrier V/W.

System 4 As contemplated herein, the chemical formulation of the t invention may comprise at least one organic acid and at least one ester. In a preferred embodiment, the at least one acid is propanoic acid. In one embodiment, the at least one ester is isoamyl formate. In another embodiment, the at least one ester may be any single carbon (acid) ent ester. In one embodiment, the chemical formulation comprises propanoic acid and isoamyl formate. In certain embodiments, the formulation may additionally comprise cineole, ene, salts or any other additive, ent or other component desired to produce a formulation having the desired characteristic.

In one embodiment, the ratio of propanoic acid: isoamyl formate is about 7:2 v/v. It should be appreciated that the chemical formulation of System 4 is not limited to any ular ratio of such chemical components. In another ment, the chemical formulation of System 4 consists of a single organic acid component and a single ester component. In such an embodiment, the formulation consists of propanoic acid: isoamyl formate at the ratios described above. In one embodiment, the chemical formulation consists essentially of propanoic acid and isoamyl formate at a ratio of propanoic acid:isoamyl formate of about 7:2 v/v.

As contemplated herein, the present invention may include any al formulation of System 4 plus the on of at least one endophytic fungus. As trated herein, endophytic fungi of the group F. subglutinans and others are particularly suited to grow on and degrade human wastes. In addition, the fungus is only able to grow on the liquid and solid waste combination when another antimicrobial mixture such as System 4 is applied and this e maximally allows for fungal growth whilst killing bacteria and other microbes. In one embodiment, the fungus is 'um subglutinans. In yet another embodiment, the present invention includes a chemical formulation comprising a 7:2 mixture of propanoic acid and isoamyl formate, and optionally with the addition of a Fusarz'um subglutinans. In this ment, the propanoic acid/isoamyl formate e is suitable for killing selected microorganisms without g the Fusarium spp., which can further enhance the recycling of a waste product to which the formulation is applied. In one embodiment, the fungus is incorporated into System 4 via inoculated barley.

In one embodiment, System 4 includes propanoic acid: l formate in the ratio of 7: 2 v/v, which is then added at the rate of 1/10 V/W of the mixture to the dry weight of the carrier substance such as bentonite, e or zeolite etc. Barley inoculated with Fusarz'um subglutinans may also be added. This mixture is then added to a ner, such as a plastic bag, used to treat and dispose of human wastes. It allows for the rapid growth ofFusarl'um subglutinans. Other items may also be added to the bag including liquid absorbing polymers in appropriate amounts, as would be understood by those skilled in the art.

System 5 As bed elsewhere herein, the chemical formulation may comprise two organic acids and at least one ester. For example, in one embodiment, the ation includes oic acid: isobutryic acid: isoamyl hexanoates. In one embodiment, the ratio of oic acid: isobutryic acid: isoamyl hexanoates is about 3.5:3.5:2 v/v/v. In another ment, the mixture of propanoic acid: ryic acid: isoamyl hexanoates is about 7 parts of the two acids and 2 parts of the selected ester. It should be appreciated that the chemical formulation of System 5 is not limited to any particular ratio of such chemical components. In another embodiment, the chemical formulation of System 5 consists of only two organic acids and a single ester. In such an embodiment, the formulation ts of propanoic acid: isobutryic acid: isoamyl hexanoates at the ratios described above. In certain embodiments, the formulation may additionally comprise cineole, valencene, salts or any other additive, excipient or other component desired to produce a ation having the desired characteristic.

In another embodiment, the chemical formulation of System 5 may be added to a carrier such as, without limitation, bentonite, zeolite, perlite or other silica based carriers, in amounts that are effective in killing bacteria and reducing harmful and s odors.

System X As contemplated herein, the present invention may include any chemical formulation of Systems l-5 in combination with at least one of a salt, excipient, nutritional additive or supplement. In a preferred embodiment, the chemical formulation is System 3. As demonstrated herein, a chemical formulation sing System 3, at least one nutritional supplement, and at least one salt is useful for treating diseases and disorders associated with a ial infection. 2014/045297 Examples of nutritional supplements include, but are not limited to, sugars such as glucose, sucrose, or fructose, amino acids such as glycine, and protein sources such as whey protein. Any protein source may be used, as would be understood by one skilled in the art. Non-limiting examples of salts e potassium chloride, sodium chloride, magnesium sulfate, monopotassium phosphate, potassium sulfate, and magnesium acetate. Salts are useful in the formulations of the invention as they enhance electrolyte balance in a subject. Any amount of salt may be used in the compositions of the inventions. It is preferred that the amount of salt is greater than 0%. The presence of System 3 inhibits and kills pathogenic bacteria. In one embodiment, System X includes the chemical formulation of System 3, glucose, whey n, potassium chloride, magnesium sulfate, and sodium chloride. In another embodiment, System X includes the chemical formulation of System 3, glucose, glycine, potassium chloride, sodium chloride, and magnesium acetate. In r embodiment, System X es the chemical formulation of System 3, glucose, e, potassium chloride, sodium de, magnesium acetate, and tassium phosphate. It should be appreciated that the al formulation of System X is not limited to any ular ratio of such chemical components. In one ment, the amount of organic acid is about 100% and the amount of ester is 0%. In another embodiment, the amount of organic acid is about 99% and the amount of ester is about 1%. In another embodiment, the amount of organic acid is about 1% and the amount of ester is about 99%.

In certain embodiments, System X is ated using one or more pharmaceutically acceptable excipients or carriers. Examples of pharmaceutically acceptable carriers include cremophor, or any other biological surfactant as would be understood by one skilled in the art. In one embodiment, the pharmaceutically acceptable carrier is cremophor. In one embodiment, System X includes the chemical formulation of System 3 and cremophor.

In certain embodiments, Systems 2 and 4 may be used with or without a carrier to treat animal wastes (including human waste) in the presence ofFusarl'um subglutinans. In such embodiments, the present invention inhibits and kills bacteria while at the same time ng for the growth of the F. subglutinans that will eventually break down or cause decay of the solid material in the human waste.

In certain embodiments, the ae of the present invention are used to fumigate seeds that are contaminated with a microorganism.

In certain embodiments, the formulae of the present invention are administered as a gaseous formula without water or any additional carriers.

Methods Decontaminating human wastes is only one problem associated with the waste treatment process. An additional problem addressed by the present invention is the need to begin the ate degradation process of the c material in the solid and liquid wastes. The biology and biochemistry that occurs when solid and liquid wastes combine is complex. It turns out the urea in urine is immediately attacked by the enzyme urease found in most microbes associated with solid waste with the concomitant production of ammonia gas. The gas itself is harmful and produces an awful odor. Also it is lethal to most fungi as it causes an increase in pH.

Thus if one wishes to cause waste degradation, it is essential to stop ammonia production which is desirable for fungal growth and for ammonia remediation in the nment. Each of Systems l-4 cause killing and inhibition of bacterial grth and subsequent ammonia production, and Systems 2 and 4 further allows for the ready growth ofFusarz'um subglutinans which then degrades the waste. Thus, s 1 and 3 are particularly suited to treat animal bedding, wastes etc. with the reduction of ammonia.

The discovery of the appropriate rganism to bring about the rapid decay of human and animal waste began with the consideration that microbes living within plants (namely, the endophytes) would be an appropriate place to begin the search. ytes are the first microbes that are involved in the degradation of a plant when it dies of either natural causes or environmental damage. They have a set of s that degrades the cellulose, lignin and hemicelluloses found in plant materials. These are the same complex organic materials that are found in human solid wastes; therefore, in order to tackle the problem with which the present application is concerned, namely, the degradation of human and animal wastes, a number of ytic microbes were located and tested for their ability to grow on both solid and liquid human wastes. In order for the microbe to degrade the waste it must either be insensitive to the a that is produced or the ammonia must be ated from the equation. Therefore, using Systems 2 and/or 4, which allows for the growth ofFusarz'um spp. and the elimination of ammonia production, it is le to devise a useable and l means to treat liquid and solid wastes.

In one aspect, the present invention includes a method of ng human or animal waste.

In one embodiment, the method comprises contacting human or animal waste with a composition of the present invention, n the composition kills or reduces bacteria growth on the human or animal waste. In one embodiment, the composition comprises a chemical formulation of the present invention. In one embodiment, the chemical formulation further ses at least one fungus. In another embodiment, the at least one fungus ses the rate of decomposition of the human or animal waste.

In another aspect, the present invention includes a method of eliminating or reducing microbial growth at a treatment site. In one embodiment, the method comprises contacting the treatment site with a composition of the present invention, wherein the ition kills or reduces bacteria growth on the human or animal waste. In one embodiment, the composition comprises a chemical formulation of the t invention. In one embodiment, the chemical formulation further comprises at least one fungus.

In another aspect, the present invention includes a method of eliminating or reducing odor formation at a ent site. In one embodiment, the method comprises contacting the treatment site with a composition of the present invention, n the composition eliminates or reduces odor formation on the human or animal waste.

In another aspect, the present invention includes a method of eliminating or reducing the amount of ammonia at a treatment site. In one embodiment, the method ses contacting the treatment site with a composition of the t invention, wherein the composition eliminates or reduces the amount of ammonia on the human or animal waste.

In another aspect, the present invention includes a method of ting seeds that are contaminated with a microorganism. In one embodiment, the method comprises contacting the seeds with a composition of the present invention, wherein the composition reduces or eliminates microbial growth on the seeds, and in some embodiments, reduces or eliminates microbial growth on the seeds without cantly disrupting germination.

In n embodiments, the ae of the present invention may be used in hospital areas to treat human wastes in combination with a carrier to be placed in bed pans to stop contamination of the area with fecal bacteria. In certain embodiments the formulae of the t invention may be used as an antiseptic to treat cuts and wounds and surface infections in animals and . For example, the present invention may be used to treat bacterial and viral gut infections in people and animals. It is to be noted that all ingredients of Systems 1-4 are GRAS listed and as such are safe. In particular, 10 ml of 8-3 has been ed by a human with no e effects. The compositions and formulations of the present ion may also be used to treat or disinfect the surfaces of inanimate or non-living objects, or to spray or apply topically to all types of plants, such as ltural fruits, vegetables, grains and the like, or to be applied topically, ingested or inhaled by any type of animal, such as livestock or humans.

In one aspect, the present invention includes a method of ving a fruit. In one embodiment, the method comprises administering to the fruit an effective amount of a composition of the present invention. In one embodiment, the fruit is a raspberry or a grape.

In n embodiments, the formulae of the present invention, and ably S-3, may be used to disinfest corn that is used for the fermentation to alcohol.

Mastitis is an infection of the tissues of a cow’s udder. Almost any bacterial or mycotic organism that can opportunistically invade tissue and cause infection can cause mastitis. It represents one of the most ant problems in dairy production. Most mastitis infections are caused by various species of streptococci, staphylococci, and gram-negative rods, especially lactose-fermenting organisms of enteric origin, commonly termed coliforms and these include such organisms as E. coli and Staphlycoccus aureus. From an epidemiologic standpoint, the source of infection may be regarded as contagious or environmental and cows are in constant threat of getting infected with these agents.

Except for Mycoplasma spp, which may spread from cow to cow through l transmission and invade the udder uent to bacteremia, contagious pathogens are spread during milking by milkers' hands or the liners of the milking unit. The chief bacterial species that utilize this mode of transmission include Staphylococcus aureus, Streptococcus tiae, and bacterium bovis. Most other species are unistic invaders from the cow's environment, although some other streptococci and staphylococci may also have a contagious component.

Intramammary infections are often described as subclinical or clinical mastitis.

Subclinical mastitis is the presence of an infection without apparent signs of local inflammation or systemic involvement. Although transient episodes of abnormal milk or udder inflammation may appear, these infections are for the most part asymptomatic and, if the infection persists for at least 2 months, are termed chronic. Once established, many of these infections persist for entire lactations or the life of the cow. Detection is best done by ation of milk for somatic cell counts (predominantly neutrophils) using either the California Mastitis Test or automated methods provided by dairy herd improvement organizations. Somatic cell counts are positively correlated with the presence of infection. Although variable (especially if determined on a single analysis), cows with a somatic cell count of 2280,000 mL (Z a linear score of 5) have a >80% chance of being infected. Likewise, the higher the somatic cell count in a herd bulk tank, the higher the prevalence of infection in the herd. Causative agents must be fied by bacterial culture of milk.

Clinical mastitis is an inflammatory response to infection causing visibly abnormal milk (eg, color, fibrin clots). As the extent of the inflammation increases, changes in the udder ing, heat, pain, redness) may also be apparent. Clinical cases that include only local signs are referred to as mild or moderate. If the inflammatory response es systemic involvement (fever, ia, , the case is termed . If the onset is very rapid, as often occurs with severe clinical cases, it is termed an acute case of severe mastitis. More severely affected cows tend to have more serous secretions in the affected quarter.

Although any number of quarters can be infected simultaneously in nical mastitis, lly only one quarter at a time will display clinical mastitis. However, it is not uncommon for clinical episodes caused by asma to affect multiple quarters. Gangrenous mastitis can also occur, particularly when subclinical, chronic infections of S aureus become severe at times of immunosuppression (eg, at parturition). As with nical mastitis, culture of milk samples collected from affected quarters is the only reliable method to determine the etiology of clinical cases.

All dairy herds have cows with subclinical mastitis; however, the prevalence of infected cows varies from 15—75%, and quarters from 5—40%. Many different pathogens can establish a chronic ion that will only on occasion st clinical signs of mastitis. The primary focus of most subclinical mastitis programs is to reduce the prevalence of the contagious pathogens Streptococcus agalactiae and Staphylococcus aureus, as well as other gram-positive cocci, most notably Streptococcus dysgalactz'ae (which may also be contagious or an environmental pathogen), Streptococcus uberz’s, enterococci, and numerous other coagulase-negative staphylococci, including S hyz’cus, S epidermidis, S xylosus, and S intermedius.

For contagious pathogens, adult lactating cattle are most at risk for infection, either while lactating or during the dry . The primary reservoir of infection is the mammary gland; transmission occurs at milking with either milkers' hands or milking equipment acting as fomites. Primiparous s have been ed to be infected with staphylococci and streptococci prior to calVing, although the prevalence varies greatly among herds and geographic regions. Teat-end dermateatis caused by the horn fly, Haematobz‘a irritans, which can harbor S aureus, has been associated with increased risk of infection in s, especially in warmer climates.

Commonly used treatments include the use of antibiotics, which pose a threat to the milk being acquired from the animal since the antibiotics will make their way into the udder. Milk cannot be used for at least 3 days after the administration of the antibiotic. The use of immunization is not possible since there are a large number of potential pathogens involved in the mastitis disease. The general recommendation is for sanitation practices to be intensified with cleanliness in the milking parlor and in the areas frequented by the animals. Currently, no available treatment has been found to be both ive and safe for the treating mastitis.

In one aspect, the t invention includes a method of ng an animal haVing a disease or disorder associated with a microbial infection. In one embodiment, the method comprises administering to the animal an effective amount of a composition of the present invention. In another embodiment, the method ses administering to the animal an effective amount of a composition comprising an organic acid. Such diseases and ers may include, without limitation, diarrheal diseases such as scours, food poisoning, or stomach flu, or intramammary infections such as subclinical or clinical mastitis. It should be r appreciated that the formulae and compositions of the present invention are not limited to treatment of any particular type of subject. As contemplated herein, the subject may be any animal, preferably a mammal, and more preferably livestock, such as cattle, sheep, or swine, or even a human. In one embodiment, the animal is bovine, porcine, or ovine. In another ment, the animal is human.

In another aspect, the present invention includes a method of treating a cow haVing scours. In one embodiment, the method ses administering to the cow an effective amount of a composition of the t invention.

In another aspect, the present invention es a method of treating a pig having scours.

In one embodiment, the method comprises administering to the pig an effective amount of a composition of the present invention.

In another aspect, the present invention includes a method of treating a cow having mastitis. In one embodiment, the method comprises administering to the cow an effective amount of a composition of the present invention.

In another aspect, the present invention includes a method of treating a sheep having mastitis. In one embodiment, the method comprises administering to the sheep an effective amount of a ition of the present invention.

In another aspect, the present invention includes a method of treating a human having a diarrheal e. In one embodiment, the method comprises administering to the human an effective amount of a composition of the present invention. In one embodiment, the diarrheal disease is food poisoning or h flu.

Combination Therapy The compositions of the present invention are intended to be useful in combination with one or more additional compounds. In non-limiting es, the compositions of the invention may be used in combination with one or more therapeutic agents (or a salt, solvate or prodrug thereof). Non-limiting examples of therapeutic agents include antibiotics such as Baytril, sulfonamides, Nuflor, Tylan 40-50, Excede, Noromycin LA, Draxxin, and tetracycline, es such as Inforce 3, multivitamins, probiotics, and toxin absorbants such as Toxiban, or other therapeutic agents such as .

In another embodiment, the compositions of the invention may be used in combination with a detergent. In one embodiment, the detergent acts as a lizing agent for the composition while removing unwanted bacterial laden debris from the area of infection of the subject, and any other possible s of infection, such as bedding, tools, or places where the subject lives. In a non-limiting e, the itions of the present invention are useful for treating the udder, the bedding used for g cattle, which is the primary source of environmental pathogens, as well as tools used in the milking process which have all been identified as potential sources of infection, such as contaminated teat dips, intramammary infusions, water hoses used for udder preparation during milking, water ponds or mud holes, skin lesions, teat trauma, and flies. miting examples of detergents include Sucragel CF, Chemoxide CAW, BioSoft D40, Lathanol LAL, BioTerge AS-40, Nacconol 90G, and potassium Pharmaceutical Compositions and Therapies Administration of a composition useful within the invention may be achieved in a number of different ways, using methods known in the art. The eutic and lactic methods of the invention thus encompass the use of pharmaceutical compositions comprising the compositions useful within the ion to practice the methods of the invention. The pharmaceutical compositions useful for practicing the invention may be administered to deliver a dose of l ng/kg/day to 100 mg/kg/day.

The relative amounts of the active ingredient, the pharmaceutically acceptable carrier, and any additional ingredients in a ceutical ition of the invention will vary, depending upon the identeaty, size, and condition of the t treated and further depending upon the route by which the composition is to be administered. By way of example, the composition may comprise between 0.1% and 100% (w/w) active ingredient.

Although the description of pharmaceutical compositions provided herein are principally directed to pharmaceutical compositions that are suitable for ethical administration to humans, it will be understood by the skilled artisan that such itions are generally suitable for administration to animals of all sorts. Modification of pharmaceutical compositions suitable for administration to humans in order to render the compositions suitable for administration to various animals is well understood, and the ordinarily skilled veterinary pharmacologist can design and perform such modification with merely ordinary, if any, experimentation. ts to which administration of the pharmaceutical compositions of the invention is contemplated include, but are not limited to, humans and other primates, mammals including commercially nt mammals such as non-human primates, cattle, pigs, horses, sheep, cats, and dogs. lly, dosages which may be administered in a method of the invention to an animal, preferably a human, range in amount from 0.5 ug to about 50 mg per kilogram of body weight of the animal. While the precise dosage administered will vary depending upon any number of factors, including but not d to, the type of animal and type of disease state being treated, the age of the animal and the route of administration, the dosage of the composition will preferably vary from about 1 ug to about 10 mg per am of body weight of the animal.

More preferably, the dosage will vary from about 3 ug to about 1 mg per am of body weight of the animal. ceutical compositions that are useful in the methods of the invention may be prepared, packaged, or sold in compositions suitable for oral, parenteral, topical, buccal, or another route of administration. Other contemplated itions include projected nanoparticles, liposomal preparations, resealed erythrocytes containing the active ingredient, and immunologically-based compositions.

The pharmaceutical compositions described herein may be prepared by any method known or hereafter developed in the art of pharmacology. In general, such preparatory methods include the step of bringing the active ingredient into association with a pharmaceutically acceptable carrier or one or more other accessory ingredients, and then, if necessary or desirable, shaping or packaging the t into a d single- or multi-dose unit.

A pharmaceutical composition of the invention may be prepared, packaged, or sold in bulk, as a single unit dose, or as a plurality of single unit doses. As used herein, a “unit dose” is discrete amount of the pharmaceutical composition comprising a predetermined amount of the active ingredient. The amount of the active ingredient is generally equal to the dosage of the active ingredient that would be administered to a subject or a convenient fraction of such a dosage such as, for example, one-half or one-third of such a dosage.

In one embodiment, the compositions of the invention are ated using one or more pharmaceutically acceptable excipients or carriers. In one embodiment, the pharmaceutical compositions of the invention comprise a therapeutically effective amount of a composition of the invention and a pharmaceutically able carrier. ceutically acceptable carriers that are useful, include, but are not limited to, glycerol, water, saline, ethanol and other pharmaceutically acceptable salt solutions such as phosphates and salts of organic acids.

Examples of these and other pharmaceutically acceptable carriers are described in Remington’s Pharmaceutical Sciences (1991, Mack ation Co., New Jersey).

The carrier may be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, ene glycol, and liquid polyethylene , and the like), suitable mixtures thereof, and vegetable oils. The proper fluidity may be maintained, for example, by the use of a g such as lecithin, by the maintenance of the ed particle size in the case of dispersion and by the use of surfactants. Prevention of the action of microorganisms may be achieved by various antibacterial and antifungal agents, for e, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, sodium chloride, or polyalcohols such as mannitol and sorbitol, in the composition. Prolonged absorption of the injectable itions may be brought about by including in the composition an agent that delays tion, for example, aluminum earate or gelatin. In one embodiment, the pharmaceutically acceptable r is not DMSO alone.

Compositions may be employed in admixtures with conventional excipients, i.e., pharmaceutically acceptable organic or inorganic carrier substances le for oral, parenteral, nasal, intravenous, subcutaneous, enteral, or any other suitable mode of administration, known to the art. The pharmaceutical preparations may be sterilized and if desired mixed with ary agents, e. g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure buffers, coloring, ng and/or aromatic substances and the like.

They may also be combined where desired with other active agents, e.g., other analgesic agents.

As used herein, “additional ingredients” include, but are not limited to, one or more of the following: excipients; e active ; dispersing agents; inert diluents; granulating and disintegrating agents; binding agents; lubricating agents; sweetening agents; flavoring agents; coloring agents; preservatives; physiologically degradable compositions such as gelatin; aqueous vehicles and solvents; oily vehicles and solvents; suspending agents; dispersing or wetting agents; emulsifying agents, demulcents; buffers; salts; thickening agents; ; emulsifying agents; antioxidants; antibiotics; antifungal agents; stabilizing agents; and pharmaceutically acceptable polymeric or hydrophobic materials. Other “additional ingredients” that may be included in the pharmaceutical compositions of the invention are known in the art and bed, for e in Genaro, ed. (1985, Remington’s Pharmaceutical Sciences, Mack hing Co., Easton, PA), which is incorporated herein by reference.

The pharmaceutical composition of the invention may comprise a vative from about 0.005% to 2.0% by total weight of the composition. The preservative is used to prevent spoilage in the case of exposure to contaminants in the environment. Examples of preservatives useful in accordance with the invention included but are not limited to those selected from the group consisting of benzyl l, sorbic acid, parabens, imidurea and ations thereof A 2014/045297 particularly preferred preservative is a ation of about 0.5% to 2.0% benzyl alcohol and 0.05% to 0.5% sorbic acid.

The pharmaceutical composition preferably includes an xidant and a chelating agent that inhibits the degradation of the formulation. Preferred idants for some formulation are BHT, BHA, alpha-tocopherol and ascorbic acid in the preferred range of about 0.01% to 0.3% and more preferably BHT in the range of 0.03% to 0.1% by weight by total weight of the composition. Preferably, the chelating agent is present in an amount of from 0.01% to 0.5% by weight by total weight of the ition. Particularly preferred chelating agents include edetate salts (e.g. disodium edetate) and citric acid in the weight range of about 0.01% to 0.20% and more preferably in the range of 0.02% to 0.10% by weight by total weight of the composition. The chelating agent is useful for chelating metal ions in the composition that may be detrimental to the shelf life of the formulation. While BHT and disodium edetate are the particularly preferred antioxidant and ing agent respectively for some formulations, other suitable and equivalent antioxidants and chelating agents may be substeatuted therefore as would be known to those skilled in the art.

Liquid sions may be prepared using conventional methods to achieve suspension of the active ingredient in an aqueous or oily vehicle. Aqueous vehicles include, for example, water, and isotonic saline. Oily vehicles include, for example, almond oil, oily esters, ethyl alcohol, vegetable oils such as arachis, olive, sesame, or coconut oil, fractionated vegetable oils, and mineral oils such as liquid paraffin. Liquid sions may further comprise one or more additional ingredients including, but not limited to, suspending agents, dispersing or wetting agents, emulsifying , demulcents, preservatives, buffers, salts, flavorings, coloring agents, and sweetening agents. Oily suspensions may r se a thickening agent. Known ding agents include, but are not limited to, sorbitol syrup, hydrogenated edible fats, sodium alginate, polyvinylpyrrolidone, gum anth, gum acacia, and cellulose derivatives such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose.

Known dispersing or wetting agents include, but are not limited to, naturally-occurring phosphatides such as lecithin, condensation products of an alkylene oxide with a fatty acid, with a long chain tic alcohol, with a partial ester derived from a fatty acid and a hexitol, or with a partial ester derived from a fatty acid and a hexitol ide (e.g., polyoxyethylene stearate, heptadecaethyleneoxycetanol, polyoxyethylene sorbitol monooleate, and polyoxyethylene 2014/045297 sorbitan monooleate, respectively). Known emulsifying agents include, but are not limited to, lecithin, and acacia. Known preservatives include, but are not d to, methyl, ethyl, or n- -para- hydroxybenzoates, ascorbic acid, and sorbic acid. Known sweetening agents include, for example, glycerol, propylene glycol, sorbitol, sucrose, and saccharin. Known thickening agents for oily suspensions include, for example, beeswax, hard paraffin, and cetyl alcohol.

Liquid solutions of the active ingredient in aqueous or oily solvents may be prepared in substantially the same manner as liquid suspensions, the y difference being that the active ingredient is dissolved, rather than ded in the solvent. As used herein, an “oily” liquid is one which comprises a carbon-containing liquid molecule and which exhibits a less polar character than water. Liquid solutions of the pharmaceutical composition of the invention may se each of the components described with regard to liquid suspensions, it being tood that suspending agents will not necessarily aid dissolution of the active ingredient in the solvent. Aqueous solvents include, for example, water, and isotonic saline. Oily solvents include, for example, almond oil, oily , ethyl l, vegetable oils such as s, olive, sesame, or coconut oil, fractionated vegetable oils, and mineral oils such as liquid paraffin.

Powdered and granular formulations of a pharmaceutical preparation of the invention may be prepared using known methods. Such formulations may be administered directly to a subject, used, for example, to form tablets, to fill capsules, or to prepare an aqueous or oily suspension or solution by addition of an aqueous or oily vehicle thereto. Each of these formulations may further comprise one or more of dispersing or wetting agent, a suspending agent, and a preservative. Additional excipients, such as fillers and sweetening, flavoring, or coloring agents, may also be included in these formulations.

A pharmaceutical composition of the ion may also be prepared, packaged, or sold in the form of oil-in—water emulsion or a water-in-oil emulsion. The oily phase may be a vegetable oil such as olive or arachis oil, a mineral oil such as liquid paraffin, or a combination of these. Such compositions may further comprise one or more emulsifying agents such as naturally ing gums such as gum acacia or gum tragacanth, lly-occurring phosphatides such as soybean or lecithin phosphatide, esters or partial esters derived from combinations of fatty acids and hexitol ides such as sorbitan eate, and condensation products of such partial esters with ethylene oxide such as polyoxyethylene an monooleate. These emulsions may also contain additional ingredients including, for e, sweetening or flavoring agents.

Methods for impregnating or coating a al with a chemical composition are known in the art, and include, but are not limited to methods of depositing or binding a chemical composition onto a surface, methods of incorporating a chemical composition into the structure of a material during the synthesis of the al (i.e., such as with a physiologically degradable material), and methods of absorbing an aqueous or oily solution or suspension into an absorbent material, with or t subsequent drying.

Controlled- or sustained-release formulations of a composition of the ion may be made using conventional technology, in on to the sure set forth elsewhere herein. In some cases, the dosage forms to be used can be provided as slow or controlled-release of one or more active ingredients therein using, for example, hydropropylmethyl cellulose, other polymer matrices, gels, permeable membranes, c systems, multilayer coatings, microparticles, liposomes, or microspheres or a combination thereof to e the desired e profile in varying proportions. Suitable controlled-release formulations known to those of ordinary skill in the art, including those described , can be readily selected for use with the itions of the invention.

Controlled-release of an active ient can be stimulated by various inducers, for example pH, temperature, enzymes, water, or other physiological conditions or compounds. The term “controlled-release component” in the context of the present invention is defined herein as a compound or compounds, including, but not limited to, polymers, polymer matrices, gels, permeable nes, liposomes, nanoparticles, or microspheres or a combination thereof that facilitates the controlled-release of the active ingredient.

Administration/Dosing The regimen of administration may affect what consteatutes an effective amount. The therapeutic formulations may be administered to the subject either prior to or after a diagnosis of disease. Further, several divided dosages, as well as staggered dosages may be administered daily or sequentially, or the dose may be continuously infused, or may be a bolus injection.

Further, the dosages of the therapeutic formulations may be tionally increased or decreased as indicated by the exigencies of the therapeutic or prophylactic situation.

WO 03082 Administration of the compositions of the present invention to a subject, ably a mammal, more ably a human, may be d out using known procedures, at dosages and for periods of time effective to prevent or treat disease. An effective amount of the therapeutic composition necessary to achieve a therapeutic effect may vary according to factors such as the activity of the particular composition employed; the time of administration; the rate of excretion of the composition; the duration of the treatment; other drugs, compositions or materials used in combination with the composition; the state of the disease or er, age, sex, weight, condition, general health and prior medical history of the subject being treated, and like factors well-known in the medical arts. Dosage regimens may be adjusted to provide the optimum eutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation. A non- limiting example of an effective dose range for a therapeutic composition of the invention is from about 1 and 5,000 mg/kg of body weight/per day. One of ry skill in the art would be able to study the relevant factors and make the determination regarding the ive amount of the therapeutic composition without undue experimentation.

The composition may be administered to an animal as frequently as several times daily, or it may be administered less frequently, such as once a day, once a week, once every two weeks, once a month, or even less frequently, such as once every several months or even once a year or less. The frequency of the dose will be readily apparent to the skilled n and will depend upon any number of factors, such as, but not limited to, the type and severity of the disease being treated, the type and age of the , etc. The compositions of the pharmaceutical compositions described herein may be prepared by any method known or hereafter developed in the art of pharmacology. In general, such atory methods include the step of bringing the active ingredient into association with a carrier or one or more other accessory ingredients, and then, if necessary or desirable, shaping or packaging the product into a desired single- or multi-dose unit.

Actual dosage levels of the active ingredients in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient that is effective to achieve the desired therapeutic response for a particular subject, composition, and mode of administration, without being toxic to the subject.

A medical doctor, e.g., physician or veterinarian, having ordinary skill in the art may readily determine and prescribe the effective amount of the pharmaceutical composition required. For example, the ian or veterinarian could start doses of the itions of the invention employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved.

In particular embodiments, it is ally advantageous to formulate the composition in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically te units suited as unitary s for the subjects to be treated; each unit containing a predetermined quanteaty of therapeutic composition calculated to produce the desired therapeutic effect in association with the required pharmaceutical vehicle. The dosage unit forms of the invention are dictated by and ly ent on (a) the unique characteristics of the therapeutic composition and the ular therapeutic effect to be achieved, and (b) the limitations nt in the art of compounding/formulating such a therapeutic composition for the treatment of a disease in a subject.

In one embodiment, the compositions of the invention are administered to the subject in dosages that range from one to five times per day or more. In another embodiment, the compositions of the invention are administered to the subject in range of dosages that include, but are not limited to, once every day, every two, days, every three days to once a week, and once every two weeks. It will be readily apparent to one skilled in the art that the frequency of administration of the various combination compositions of the invention will vary from t to subject depending on many factors including, but not limited to, age, disease or disorder to be d, gender, overall health, and other factors. Thus, the invention should not be ued to be limited to any particular dosage regime and the precise dosage and ition to be administered to any subject will be determined by the attending physical taking all other factors about the subject into account.

Compositions of the invention for administration may be in the range of from about 0.1 mg to about 1,000 mg, about 0.2 mg to about 950 mg, about 0.4 mg to about 900 mg, about 1 mg to about 850 mg, about 5 mg to about 750 mg, about 20 mg to about 700 mg, about 30 mg to about 600 mg, about 50 mg to about 500 mg, about 75 mg to about 400 mg, about 100 mg to about 300 mg, about 120 mg to about 250 mg, and any and all Whole or partial increments therebetween.

In some embodiments, the dose of a composition of the invention is from about 1 mg and about 2,500 mg. In some embodiments, a dose of a composition of the invention used in compositions described herein is less than about 10,000 mg, or less than about 8,000 mg, or less than about 6,000 mg, or less than about 5,000 mg, or less than about 3,000 mg, or less than about 2,000 mg, or less than about 1,000 mg, or less than about 500 mg, or less than about 200 mg, or less than about 50 mg. Similarly, in some embodiments, a dose of a second composition (i.e., a drug used for ng the same or r disease as that treated by the compositions of the invention) as described herein is less than about 1,000 mg, or less than about 800 mg, or less than about 600 mg, or less than about 500 mg, or less than about 400 mg, or less than about 300 mg, or less than about 200 mg, or less than about 100 mg, or less than about 50 mg, or less than about 40 mg, or less than about 30 mg, or less than about 25 mg, or less than about 20 mg, or less than about 15 mg, or less than about 10 mg, or less than about 5 mg, or less than about 2 mg, or less than about 1 mg, or less than about 0.5 mg, and any and all Whole or partial increments thereof.

In one embodiment, the present invention is ed to a packaged ceutical composition comprising a container holding a therapeutically effective amount of a composition of the invention, alone or in combination With a second pharmaceutical agent; and instructions for using the composition to treat, prevent, or reduce one or more symptoms of a disease in a subject.

Routes of Administration Routes of administration of any of the compositions of the invention include oral, nasal, rectal, parenteral, sublingual, ermal, ucosal (e.g., sublingual, lingual, (trans)buccal, )urethral, vaginal (e.g., trans- and perivaginally), (intra)nasal, and (trans)rectal), intravesical, intrapulmonary, intraduodenal, intragastrical, intrathecal, subcutaneous, uscular, intradermal, intra-arterial, intravenous, intrabronchial, inhalation, and topical administration.

Suitable compositions and dosage forms include, for example, tablets, es, caplets, pills, gel caps, troches, dispersions, suspensions, solutions, syrups, granules, beads, transdermal patches, gels, powders, pellets, magmas, lozenges, creams, pastes, rs, lotions, discs, suppositories, liquid sprays for nasal or oral administration, dry powder or aerosolized formulations for inhalation, compositions and formulations for intravesical stration and the like. It should be understood that the formulations and compositions that would be useful in the present invention are not limited to the ular ations and itions that are described .

Oral stration For oral application, particularly suitable are tablets, dragees, liquids, drops, itories, or capsules, caplets and gelcaps. Other formulations suitable for oral administration include, but are not limited to, a powdered or granular formulation, an aqueous or oily suspension, an aqueous or oily solution, a paste, a gel, toothpaste, a mouthwash, a coating, an oral rinse, or an emulsion. The compositions intended for oral use may be prepared according to any method known in the art and such compositions may contain one or more agents selected from the group consisting of inert, non-toxic pharmaceutically excipients that are suitable for the manufacture of tablets. Such excipients e, for example an inert diluent such as lactose; granulating and disintegrating agents such as cornstarch; binding agents such as starch; and ating agents such as magnesium stearate.

Tablets may be non-coated or they may be coated using known methods to achieve delayed egration in the intestinal tract of a subject, thereby providing sustained release and absorption of the active ingredient. By way of example, a material such as glyceryl monostearate or glyceryl distearate may be used to coat tablets. Further by way of example, tablets may be coated using methods described in US. Patents numbers 4,256,108; 4,160,452; and 874 to form cally controlled release tablets. Tablets may further comprise a sweetening agent, a flavoring agent, a coloring agent, a preservative, or some combination of these in order to provide for pharmaceutically elegant and palatable preparation.

Hard capsules comprising the active ingredient may be made using a physiologically degradable composition, such as gelatin. Such hard capsules comprise the active ingredient, and may further comprise additional ingredients including, for example, an inert solid diluent such as calcium carbonate, calcium phosphate, or kaolin.

Soft gelatin capsules comprising the active ingredient may be made using a physiologically degradable composition, such as gelatin. Such soft capsules comprise the active ingredient, which may be mixed with water or an oil medium such as peanut oil, liquid in, or olive oil.

For oral administration, the compositions of the invention may be in the form of tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding ; fillers; lubricants; disintegrates; or wetting agents. If desired, the s may be coated using suitable methods and coating materials such as TM film coating systems available from Colorcon, West Point, Pa. (e. g., OPADRYTM OY Type, OYC Type, Organic Enteric OY-P Type, Aqueous Enteric OY-A Type, OY-PM Type and TM White, 32Kl 8400).

Liquid preparation for oral administration may be in the form of solutions, syrups or suspensions. The liquid ations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g., ol syrup, methyl cellulose or hydrogenated edible fats); emulsifying agent (e.g., lecithin or acacia); non-aqueous vehicles (e.g., almond oil, oily esters or ethyl alcohol); and preservatives (e.g., methyl or propyl para-hydroxy benzoates or sorbic acid). Liquid formulations of a pharmaceutical composition of the ion which are suitable for oral administration may be ed, ed, and sold either in liquid form or in the form of a dry product intended for reconsteatution with water or another suitable vehicle prior to use.

A tablet comprising the active ingredient may, for example, be made by compressing or molding the active ingredient, ally with one or more onal ingredients. Compressed tablets may be prepared by compressing, in a suitable device, the active ingredient in a free-flowing form such as a powder or granular preparation, optionally mixed with one or more of a binder, a lubricant, an excipient, a surface active agent, and a dispersing agent. Molded tablets may be made by molding, in a suitable device, a mixture of the active ingredient, a pharmaceutically acceptable carrier, and at least sufficient liquid to moisten the mixture.

Pharmaceutically acceptable excipients used in the manufacture of tablets include, but are not limited to, inert diluents, granulating and disintegrating agents, binding agents, and lubricating agents. Known dispersing agents include, but are not limited to, potato starch and sodium starch glycollate. Known surface-active agents include, but are not limited to, sodium lauryl sulphate.

Known diluents include, but are not limited to, calcium carbonate, sodium carbonate, lactose, microcrystalline cellulose, calcium phosphate, calcium hydrogen phosphate, and sodium phosphate. Known granulating and disintegrating agents include, but are not limited to, corn starch and c acid. Known binding agents include, but are not limited to, gelatin, acacia, pre-gelatinized maize starch, polyvinylpyrrolidone, and hydroxypropyl methylcellulose. Known lubricating agents include, but are not limited to, magnesium stearate, stearic acid, silica, and talc.

Granulating techniques are well known in the pharmaceutical art for modifying starting powders or other particulate materials of an active ingredient. The powders are typically mixed with a binder material into larger permanent free-flowing agglomerates or granules referred to as a “granulation.’ For e, solvent-using “wet” granulation processes are generally characterized in that the powders are ed with a binder material and moistened with water or an organic solvent under conditions resulting in the formation of a wet granulated mass from which the solvent must then be evaporated.

Melt granulation generally consists in the use of materials that are solid or olid at room temperature (i.e. having a vely low softening or melting point range) to promote granulation of powdered or other als, essentially in the absence of added water or other liquid solvents. The low melting solids, when heated to a temperature in the g point range, liquefy to act as a binder or granulating medium. The liquefied solid spreads itself over the surface of powdered materials with which it is ted, and on cooling, forms a solid granulated mass in which the initial materials are bound together. The resulting melt granulation may then be provided to a tablet press or be encapsulated for preparing the oral dosage form.

Melt granulation es the dissolution rate and bioavailability of an active (i.e. drug) by forming a solid dispersion or solid solution.

US. Patent No. 645 discloses directly compressible wax-containing granules having ed flow properties. The granules are obtained when waxes are admixed in the melt with certain flow improving additives, ed by cooling and granulation of the admixture. In certain embodiments, only the wax itself melts in the melt combination of the wax(es) and additives(s), and in other cases both the wax(es) and the additives(s) will melt.

The present invention also includes a multi-layer tablet comprising a layer ing for the delayed release of one or more compositions of the invention, and a r layer providing for the immediate release of a medication for treatment of a e. Using a wax/pH-sensitive polymer mix, a gastric insoluble composition may be obtained in which the active ingredient is entrapped, ensuring its delayed release.

Parenteral Administration As used herein, teral administration” of a pharmaceutical composition includes any route of administration characterized by physical breaching of a tissue of a subject and administration of the pharmaceutical composition through the breach in the . Parenteral administration thus includes, but is not limited to, administration of a pharmaceutical composition by injection of the composition, by ation of the composition through a al incision, by application of the composition through a tissue-penetrating non-surgical wound, and the like. In particular, parenteral administration is contemplated to include, but is not d to, intraocular, intravitreal, aneous, intraperitoneal, intramuscular, intrastemal injection, intratumoral, and kidney dialytic infusion techniques.

Formulations of a pharmaceutical composition suitable for parenteral administration comprise the active ingredient combined with a pharmaceutically acceptable r, such as sterile water or sterile isotonic saline. Such formulations may be prepared, packaged, or sold in a form suitable for bolus administration or for continuous administration. able formulations may be prepared, packaged, or sold in unit dosage form, such as in ampules or in multi-dose containers containing a preservative. Formulations for parenteral administration include, but are not limited to, suspensions, solutions, emulsions in oily or aqueous vehicles, pastes, and table sustained-release or biodegradable formulations. Such formulations may further comprise one or more additional ingredients including, but not d to, suspending, stabilizing, or dispersing agents. In one ment of a formulation for parenteral stration, the active ingredient is provided in dry (i.e. powder or granular) form for reconsteatution with a suitable vehicle (e.g. sterile pyrogen-free water) prior to parenteral administration of the teatuted composition.

The pharmaceutical compositions may be prepared, packaged, or sold in the form of a sterile injectable aqueous or oily suspension or solution. This suspension or solution may be formulated according to the known art, and may comprise, in addition to the active ingredient, onal ingredients such as the dispersing agents, wetting agents, or suspending agents described herein. Such sterile injectable formulations may be prepared using a non-toxic parenterally-acceptable diluent or solvent, such as water or l,3-butanediol, for e. Other able diluents and solvents include, but are not limited to, Ringer's solution, isotonic sodium chloride solution, and fixed oils such as synthetic mono- or di-glycerides. Other parentally-administrable formulations that are useful include those which comprise the active ingredient in microcrystalline form, in a liposomal preparation, or as a component of a biodegradable polymer systems. Compositions for sustained e or implantation may comprise pharmaceutically acceptable polymeric or hydrophobic als such as an emulsion, an ion exchange resin, a sparingly soluble polymer, or a sparingly soluble salt.

Topical Administration A pharmaceutical composition of the invention may be prepared, ed, or sold in a formulation suitable for topical administration. There are several advantages to delivering compositions, including drugs or other therapeutic agents, into the skin (dermal drug ry) or into the body through the skin (transdermal drug delivery). Transdermal composition delivery offers an attractive alternative to injections and oral medications. Dermal composition delivery offers an efficient way to deliver a composition to the skin of a mammal, and preferably a human, and provides a method of treatment of the skin, or otherwise provides a method of affecting the skin, without the need to break or damage the outer layer of the skin. In the present invention, dermal delivery, by way of a dermally-acting composition of the invention, provides these advantages for ent of a skin-related condition, disorder or disease.

A number of compounds, including some drugs, will penetrate the skin effectively simply because the molecules are relatively small and potent at small doses of 0.1 mg to 15 mg/day (Kanikkannan et al., 2000, Curr. Med. Chem. 7:593-608). Many other compounds and drugs can be delivered only when an additional enhancement system is provided to ” them to pass through the skin. Among several methods of transdermal drug delivery are electroporation, oresis, horesis, tion ers (cyclodextrins), and liposomes. While the aforementioned s are also included in the present ion for dermal delivery of the compositions of the invention, liposomes represent a red dermal delivery method.

The ition of the invention may consist of the active ingredient alone, in a form suitable for administration to a subject, or the composition may comprise at least one active ingredient and one or more pharmaceutically acceptable rs, one or more additional ingredients, or some combination of these. The active ient may be present in the composition in the form of a physiologically acceptable ester or salt, such as in combination with a physiologically acceptable cation or anion, as is well known in the art. Compositions of the invention will also be understood to encompass pharmaceutical compositions useful for treatment of other conditions, disorders and diseases associated with the skin.

In one aspect, a dermal delivery vehicle of the invention is a composition comprising at least one first compound that can facilitate dermal ry of at least one second compound associated with, or in close physical proximity to, the composition comprising the first compound. As will be understood by the skilled n, when armed with the disclosure set forth , such delivery vehicles e, but should not be limited to, liposomes, nanosomes, phospholipid-based non-liposome compositions (eg., selected cochleates), among .

Formulations suitable for topical administration include, but are not limited to, liquid or semi-liquid preparations such as liniments, lotions, oil-in-water or water-in-oil emulsions such as creams, ointments or , and solutions or suspensions. Topically-administrable formulations may, for example, comprise from about 0.001% to about 90% (w/w) active ingredient, although the concentration of the active ingredient may be as high as the lity limit of the active ingredient in the solvent. Formulations for topical administration may further comprise one or more of the additional ients described herein.

In one aspect of the invention, a dermal delivery system es a liposome delivery system, and that the t invention should not be construed to be limited to any ular liposome delivery system. Based on the disclosure set forth herein, the skilled artisan will understand how to identify a liposome delivery system as being useful in the present invention.

The present invention also encompasses the improvement of dermal and transdermal drug delivery through the use of penetration enhancers (also called sorption promoters or accelerants), which penetrate into skin to reversibly decrease the barrier resistance. Many compounds are known in the art for penetration enhancing activity, including sulphoxides (such as dimethylsulphoxide, DMSO), azones (e.g. apram), pyrrolidones (for example 2- pyrrolidone, 2P), alcohols and alkanols (ethanol, or decanol), glycols (for example propylene glycol, PG, a common excipient in topically applied dosage forms), surfactants (also common in WO 03082 dosage forms) and terpenes. Other enhancers include oleic acid, oleyl alcohol, ethoxydiglycol, laurocapram, alkanecarboxylic acids, dimethylsulfoxide, polar lipids, or N-methylpyrrolidone.

In alternative ments, the topically active pharmaceutical or cosmetic composition may be optionally ed with other ients such as moisturizers, cosmetic adjuvants, anti-oxidants, chelating agents, tants, foaming agents, conditioners, humectants, wetting agents, emulsifying agents, fragrances, viscosifiers, buffering agents, preservatives, sunscreens and the like. In another embodiment, a permeation or penetration enhancer is included in the composition and is effective in ing the percutaneous penetration of the active ingredient into and through the stratum comeum with respect to a composition lacking the permeation enhancer. Various permeation enhancers, including oleic acid, oleyl alcohol, ethoxydiglycol, apram, alkanecarboxylic acids, dimethylsulfoxide, polar lipids, or N-methylpyrrolidone, are known to those of skill in the art.

In another aspect, the composition may further comprise a hydrotropic agent, which functions to increase er in the structure of the stratum comeum, and thus allows increased transport across the stratum comeum. Various hydrotropic agents such as isopropyl alcohol, ene glycol, or sodium xylene sulfonate, are known to those of skill in the art. The compositions of this invention may also n active amounts of retinoids (i.e., compounds that bind to any members of the family of retinoid receptors), including, for e, tretinoin, retinol, esters of tretinoin and/or retinol and the like.

The composition of the ion may comprise a vative from about 0.005% to 2.0% by total weight of the composition. The vative is used to prevent spoilage in the case of an aqueous gel because of repeated patient use when it is exposed to contaminants in the environment from, for example, exposure to air or the patient's skin, including contact with the fingers used for applying a composition of the invention such as a therapeutic gel or cream.

Examples of preservatives useful in accordance with the invention included but are not limited to those selected from the group consisting of benzyl alcohol, sorbic acid, parabens, imidurea and combinations thereof A particularly preferred preservative is a ation of about 0.5% to 2.0% benzyl alcohol and 0.05% to 0.5% sorbic acid.

The composition preferably includes an antioxidant and a chelating agent which inhibit the degradation of the composition for use in the invention in the aqueous gel formulation.

Preferred antioxidants for some compounds are BHT, BHA, tocopherol and ascorbic acid in the preferred range of about 0.01% to 5% and BHT in the range of 0.01% to 1% by weight by total weight of the composition. Preferably, the chelating agent is present in an amount of from 0.01% to 0.5% by weight by total weight of the composition. Particularly red chelating agents include e salts (e.g. um edetate) and citric acid in the weight range of about 0.01% to 0.20% and more preferably in the range of 0.02% to 0.10% by weight by total weight of the composition. The chelating agent is useful for chelating metal ions in the composition which may be detrimental to the shelf life of the formulation. While BHT and disodium edetate are the particularly preferred antioxidant and chelating agent respectively for some compounds, other suitable and equivalent idants and chelating agents may be substeatuted therefore as would be known to those skilled in the art.

Additional ents may include, but should not be limited to those including water, oil (eg., olive oil/PEG7), biovera oil, wax (eg., jojoba wax), squalene, myristate (eg., isopropyl myristate), triglycerides (eg., ic triglyceride), Solulan 98, cocoa butter, shea butter, alcohol (eg., behenyl alcohol), stearate (eg., glycerol-monostearate), chelating agents (eg., EDTA), propylene , SEPIGEL (Seppic, Inc., Fairfield, NJ), silicone and silicone derivatives (eg., dimethicone, cyclomethicone), vitamins (eg., vitamin E), among others.

Buccal stration A pharmaceutical ition of the invention may be prepared, packaged, or sold in a formulation suitable for buccal administration. Such formulations may, for example, be in the form of tablets or lozenges made using conventional methods, and may, for example, 0.1 to 20% (w/w) active ingredient, the balance comprising an orally dissolvable or degradable composition and, optionally, one or more of the additional ingredients described herein. Altemately, formulations suitable for buccal administration may comprise a powder or an aerosolized or atomized solution or suspension sing the active ingredient. Such ed, aerosolized, or aerosolized formulations, when dispersed, preferably have an average particle or droplet size in the range from about 0.1 to about 200 nanometers, and may further comprise one or more of the additional ingredients described herein.

Rectal Administration WO 03082 2014/045297 A pharmaceutical composition of the invention may be prepared, packaged, or sold in a formulation suitable for rectal administration. Such a ition may be in the form of, for example, a suppository, a retention enema preparation, and a solution for rectal or colonic tion.

Suppository formulations may be made by combining the active ingredient with a non- irritating pharmaceutically acceptable excipient which is solid at ordinary room temperature (i.e., about 20 0C) and which is liquid at the rectal temperature of the subject (i.e., about 37 0C in a healthy human). Suitable pharmaceutically acceptable excipients include, but are not limited to, cocoa butter, polyethylene glycols, and various glycerides. Suppository formulations may further comprise various additional ingredients including, but not d to, antioxidants, and preservatives.

Retention enema preparations or solutions for rectal or colonic irrigation may be made by combining the active ient with a pharmaceutically acceptable liquid r. As is well known in the art, enema preparations may be administered using, and may be packaged within, a delivery device adapted to the rectal anatomy of the subject. Enema ations may further comprise various additional ingredients including, but not d to, antioxidants, and preservatives.

Additional Administration Farms Additional dosage forms of this invention include dosage forms as described in US.

Patents Nos. 6,340,475; 6,488,962; 6,451,808; 5,972,389; 837 and 5,007,790. Additional dosage forms of this invention also include dosage forms as described in US. Patent Applications Nos. 47952, 20030104062, 20030104053, 44466, 20030039688, and 20020051820. Additional dosage forms of this invention also include dosage forms as described in PCT Applications Nos. WO 41, WO 03/35040, WO 03/35029, WO 03/35177, WO 03/35039, WO 02/96404, WO 02/32416, WO 01/97783, WO 01/56544, WO 01/32217, WO 98/55107, WO 98/11879, WO 85, WO 93/18755, and WO 90/11757.

Controlled Release Formulations and Drug Delivery Systems Controlled- or sustained-release formulations of a pharmaceutical composition of the invention may be made using conventional technology, using for example proteins equipped with pH sensitive domains or protease-cleavable fragments. In some cases, the dosage forms to be used can be provided as slow or controlled-release of one or more active ingredients therein using, for example, ropylmethyl cellulose, other r matrices, gels, permeable nes, osmotic systems, multilayer coatings, micro-particles, liposomes, or microspheres or a combination thereof to provide the desired release profile in g proportions. Suitable controlled-release ations known to those of ordinary skill in the art, including those described herein, can be readily selected for use with the pharmaceutical compositions of the ion. Thus, single unit dosage forms suitable for oral administration, such as tablets, capsules, gel-caps, and caplets, which are adapted for controlled-release are encompassed by the present invention.

Most controlled-release ceutical products have a common goal of improving drug therapy over that achieved by their ntrolled counterparts. Ideally, the use of an optimally ed controlled-release preparation in medical treatment is characterized by a minimum of drug substance being employed to cure or control the condition in a minimum amount of time.

Advantages of controlled-release ations include extended activity of the drug, reduced dosage frequency, and increased subject compliance. In addition, controlled-release formulations can be used to affect the time of onset of action or other characteristics, such as blood level of the drug, and thus can affect the occurrence of side effects.

Most controlled-release formulations are designed to initially release an amount of drug that promptly produces the desired therapeutic , and gradually and continually release of other amounts of drug to maintain this level of therapeutic effect over an extended period of time. In order to maintain this constant level of drug in the body, the drug must be ed from the dosage form at a rate that will replace the amount of drug being metabolized and excreted from the body.

Controlled-release of an active ingredient can be stimulated by various inducers, for example pH, ature, enzymes, water or other physiological conditions or compounds. The term “controlled-release component” in the context of the present invention is defined herein as a compound or compounds, including, but not limited to, polymers, polymer matrices, gels, permeable nes, liposomes, or microspheres or a combination thereof that facilitates the controlled-release of the active ingredient.

In certain embodiments, the formulations of the present invention may be, but are not d to, short-term, rapid-offset, as well as controlled, for example, sustained e, delayed release and pulsatile release formulations.

The term sustained release is used in its conventional sense to refer to a drug formulation that provides for gradual release of a drug over an extended period of time, and that may, although not necessarily, result in substantially constant blood levels of a drug over an extended time period. The period of time may be as long as a month or more and should be a release that is longer that the same amount of agent administered in bolus form.

For sustained release, the compositions may be formulated with a suitable polymer or hydrophobic material that provides sustained release properties to the compositions. As such, the itions for use the method of the invention may be administered in the form of microparticles, for example, by injection or in the form of wafers or discs by implantation.

In a red embodiment of the invention, the compositionss of the invention are administered to a subject, alone or in combination with another pharmaceutical agent, using a ned release formulation.

The term delayed release is used herein in its tional sense to refer to a drug ation that provides for an initial release of the drug after some delay following drug administration and that mat, although not necessarily, includes a delay of from about 10 minutes up to about 12 hours.

The term pulsatile release is used herein in its conventional sense to refer to a drug formulation that es release of the drug in such a way as to e pulsed plasma profiles of the drug after drug administration.

The term ate release is used in its conventional sense to refer to a drug formulation that provides for release of the drug immediately after drug administration.

As used herein, short-term refers to any period of time up to and including about 8 hours, about 7 hours, about 6 hours, about 5 hours, about 4 hours, about 3 hours, about 2 hours, about 1 hour, about 40 minutes, about 20 s, or about 10 minutes and any or all whole or partial increments thereof after drug administration after drug administration.

As used herein, rapid-offset refers to any period of time up to and including about 8 hours, about 7 hours, about 6 hours, about 5 hours, about 4 hours, about 3 hours, about 2 hours, about 1 hour, about 40 minutes, about 20 minutes, or about 10 minutes, and any and all whole or partial ents thereof after drug administration.

Accordingly, in one embodiment, the present ion relates to a chemical formulation comprising propanoic acid, yric acid, at least one ester, and at least one carrier, wherein the chemical formulation has antibacterial activity when applied to human or animal waste. In r embodiment, the at least one ester is isoamyl butyrate. In another embodiment, the at least one carrier is a silica based carrier. In another embodiment, the at least one carrier is selected from the group consisting of bentonite, zeolite and perlite. In another embodiment, the ratio of propanoic acid: ryic acid: isoamyl butyrate is about 3.5:3.5:2 V/V/V. In another embodiment, the ratio of oic acid, isobutryic acid and isoamyl butyrate is about 7 parts of the two acids and 2 parts of isoamyl butyrate. In another embodiment, the chemical formulation consists essentially of propanoic acid, isobutryic acid, isoamyl butyrate and a carrier. In another embodiment, the carrier is selected from the group consisting of bentonite, zeolite and perlite. In another embodiment, the chemical formulation has antibacterial actiVity when applied to human or animal waste.

In another embodiment, the present invention relates to a chemical formulation comprising, propanoic acid, isobutryic acid, at least one ester, at least one carrier, and at least one fungus. In another embodiment, the at least one ester is isoamyl te. In another embodiment, the at least one carrier is a silica based carrier. In another embodiment, the at least one r is selected from the group consisting of bentonite, e and perlite. In another embodiment, the ratio of oic acid: isobutryic acid: isoamyl butyrate is about 3.5:3.5:2 V/V/V. In another embodiment, the ratio of propanoic acid, isobutryic acid and isoamyl butyrate is about 7 parts of the two acids and 2 parts of l butyrate. In another embodiment, the at least one fungus is an endophyte. In another embodiment, the endophyte is of the genus Fusarz'um. In r embodiment, the endophyte is F. subglutinans.

In another embodiment, the present invention relates to a chemical formulation comprising propanoic acid and at least one 6-12 carbon (acid) component ester, wherein the al formulation has a ratio of propanoic acid:ester component of about 7:2 V/V. In r embodiment, the at least one ester is isoamyl hexanoates. In another embodiment, the ation r includes at least one nutritional supplement and at least one salt. In another embodiment, the formulation comprises glucose, whey protein, potassium chloride, magnesium sulfate, and sodium chloride. In another embodiment, the formulation comprises glucose, glycine, potassium chloride, sodium chloride, and ium acetate. In another embodiment, the ation comprises glucose, glycine, potassium chloride, sodium chloride, magnesium acetate, and monopotassium phosphate. In another embodiment, the formulation includes at least one pharmaceutically able carrier. In another embodiment, the carrier is cremophor. In another embodiment, the formulation consists essentially of propanoic acid and isoamyl hexanoates at a ratio of propanoic acid:isoamyl hexanoates of about 7:2 V/V. In another embodiment, the t invention relates to a chemical ation consisting essentially of propanoic acid, isoamyl hexanoates and a carrier.

In another embodiment, the present invention relates to a chemical formulation comprising propanoic acid and a single carbon (acid) component ester, wherein the chemical formulation has a ratio of propanoic acid:ester component of about 7:2 V/V. In another embodiment, the at least one ester is isoamyl formate. In another ment, the formulation consists essentially of propanoic acid and isoamyl formate at a ratio of propanoic acid:isoamyl formate of about 7:2 V/V. In another embodiment, the formulation es at least one carrier. In another embodiment, the at least one r is a silica based carrier. In another embodiment, the at least one carrier is selected from the group consisting of bentonite, zeolite and perlite. In another embodiment, the al formulation consists essentially of propanoic acid, isoamyl formate and a carrier.

In another embodiment, the present invention es a chemical formulation comprising propanoic acid, isoamyl formate, and at least one fungus. In another embodiment, the ratio of propanoic acid: l formate is about 7:2 V/V. In another embodiment, the at least one fungus is an endophyte. In another ment, the endophyte is of the genus 'um. In r embodiment, the endophyte is F. subglutinans.

In another embodiment, the present invention relates to a method of treating human or animal waste, comprising ting human or animal waste with a ition comprising propanoic acid, isobutryic acid and at least one ester, wherein the composition kills or reduces bacteria growth on the human or animal waste. In another ment, the present invention relates to a method of treating human or animal waste, comprising contacting human or animal waste with a composition comprising propanoic acid, isobutryic acid, at least one ester and at least one fungus, wherein the propanoic acid, isobutryic acid and at least one ester kills or 2014/045297 reduces bacteria growth on the human or animal waste, and the at least one fungus increases the rate of decomposition of the human or animal waste. In another embodiment, the present invention relates to a method of eliminating or reducing microbial growth at a treatment site, comprising contacting the treatment site with a composition comprising propanoic acid and at least one ester at a ratio of propanoic ster of about 7:2, wherein the ester is isoamyl formate or isoamyl hexanoates and the ition kills or reduces bacteria growth on the human or animal waste. In r ment, the present invention relates to a method of treating human or animal waste, comprising contacting human or animal waste with a composition comprising propanoic acid, isoamyl formate at a ratio of propanoic acid:isoamyl formate of about 7:2, and at least one fungus, wherein the propanoic acid and l formate mixture kills or reduces microbial growth on the human or animal waste, and the at least one fungus increases the rate of decomposition of the human or animal waste. In another embodiment, the present invention relates to a method of treating an animal having a disease or disorder associated with a microbial infection, comprising administering to the animal an effective amount of a ition comprising at least one organic acid. In another embodiment, the ition consists essentially of an organic acid. In another embodiment, the composition consists of an organic acid. In another embodiment, the at least one organic acid is propanoic acid. In another embodiment, the at least one organic acid is isobutyric acid. In another embodiment, the animal is a human. In another embodiment, the disease or disorder is a eal disease. In another embodiment, the animal is bovine, porcine, or ovine. In another embodiment, the disease or er is selected from the group consisting of a diarrheal disease and an intramammary infection. In another embodiment, the eal disease is scours. In another embodiment, the intramammary infection is nical mastitis or clinical mastitis. In another embodiment, the ition further comprises at least one ester. In another embodiment, the at least one ester is isoamyl hexanoates. In r embodiment, the composition r comprises at least one nutritional supplement and at least one salt. In another embodiment, the composition comprises glucose, whey protein, potassium chloride, magnesium sulfate, and sodium chloride. In another embodiment, the composition comprises glucose, glycine, potassium chloride, sodium chloride, and ium acetate. In another embodiment, the composition ses glucose, glycine, potassium chloride, sodium de, magnesium acetate, and monopotassium phosphate. In another embodiment, the composition further comprises at least one pharmaceutically acceptable carrier. In r embodiment, the r is cremophor. In another embodiment, the composition ses propanoic acid and isoamyl hexanoates at a ratio of propanoic acid:isoamyl hexanoates of about 7:2 v/v. In another embodiment, the at least one ester is isoamyl hexanoates. In another embodiment, the ratio of propanoic acid: isobutryic acid: isoamyl hexanoates is about 3.5:3.5:2 v/v/v. In r embodiment, the ratio of propanoic acid, isobutryic acid and isoamyl hexanoates is about 7 parts of the two acids and 2 parts of isoamyl butyrate.

In r embodiment, the present invention relates to a al formulation consisting essentially of propanoic acid, isobutryic acid, isoamyl hexanoates and a carrier. In another embodiment, the r is selected from the group consisting of bentonite, zeolite and perlite. In another ment, the chemical formulation has cterial activity when applied to human or animal waste.

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, numerous equivalents to the specific procedures, ments, claims, and examples described herein. Such equivalents were considered to be within the scope of this invention and covered by the claims appended hereto. For example, it should be understood, that modifications in on conditions, including but not limited to reaction times, reaction size/volume, and experimental reagents, such as solvents, catalysts, pressures, atmospheric conditions, e.g., nitrogen atmosphere, and reducing/oxidizing agents, with art-recognized alternatives and using no more than routine experimentation, are within the scope of the t application.

It is to be understood that wherever values and ranges are provided herein, all values and ranges encompassed by these values and ranges, are meant to be encompassed within the scope of the present invention. Moreover, all values that fall within these ranges, as well as the upper or lower limits of a range of values, are also contemplated by the present application.

The following examples further illustrate aspects of the present invention. r, they are in no way a limitation of the teachings or disclosure of the present invention as set forth herein.

EXPERIMENTAL EXAMPLES The invention is now bed with reference to the following Examples. These Examples are provided for the purpose of illustration only, and the invention is not limited to these Examples, but rather asses all ions that are evident as a result of the teachings provided herein.

Example 1 Discussed below are the various ments that resulted in the discovery of F. subglutinans and the Systems 1 and 2 which can be used in various human and animal waste treatment deVices along with animal bedding, stalls etc.

Table 1. Shows the inhibition actiVities of various esters (used in combination with a 1:1 V/V mix of oic acid and isobutryic acid and thus the two acids to esters is 7:2 V/V) to a series of test fungi and bacteria that are commonly used organisms to screen for antibiotic activities. From these data, the Systems 1 and 2 were selected for use in this invention (see highlighted areas on the Table).

Table 2. Molecular genetics data assembled on the various new Fusarz'um spp. isolates that grow on human wastes in the presence of the System 2 mixture (with carrier of bentonite or zeolite) as described above. From this it is s that any of these organisms are nearly equal or, in most cases better than Fusarz'um culmorum (P2-24), the subject of and r patent. A Data set on P2-24 is also ed.

Table 3. The growth of various fusaria on human wastes causes a ion of the dry weight of the mass during the course of a 7 week experiment. The experimental set- up contained 0.5 g of ite with System 2 on a water agar plate haVing about 100 mg wet weight of human waste and a small agar plug with the test fusarium on it. The incubation period was 7 weeks at 22 °C. The remains of the human waste were physically removed and dried for 4 hr at 80 °C and then weighed.

Figure 1. Indicates how the assays were done to yield the data sets in Table l. The various esters were combined with a 1:1 mixture of propanoic acid and isobutryic acid and these were added 7:2 V/V with the ester to be tested. Then 9 ul were placed in the center well with the indiVidual test organism agar plugs in the periphery as indicated in the Figure.

Figure 2. Demonstrates the effectiveness of System 1 (above) in killing and inhibiting human waste associated bacteria. Fresh wastes were collected and then approximately 5 mg were evenly spread on the surface of a potato se agar plate. The plates were incubated for 2 days and then photographed. The panel on the right is an untreated control, the middle contains ite 0.5 g with no antibiotic and the left contains 0.5 g with System 1.

Figure 3. Demonstrates the effectiveness of System 2 (above) in killing and inhibiting human waste associated bacteria. Fresh wastes were collected and then approximately 5 mg were evenly spread on the surface of a potato dextrose agar plate. The plates were incubated for 2 days and then photographed. The panel on the right is an untreated control, the middle contains bentonite 0.5 g with no antibiotic and the left contains 0.5 g with System 2.

Figure 4. An illustration of how treatment with System 1 can eliminate odors. Two cat litter boxes with cat fecal matter each from 5 different cats ca. 140 g. The box on the left had been treated with System 1 on ite with (0.5 ml / 100 g bentonite). After 5 days the ammonia readings were 14 ppm on the control (left) and 0 ppm on the treated right. The overall odor was significantly reduced in the treated box.

Figure 5. rates how the fungus can grow on fresh human waste and reduce the level of odor. Treatment of ca. 140 g of human waste in the ce of urine with Fusarz'um subglutinans 06-1 in the ce of System 2 ( 1 ml on 10 g of zeolite). After 3 weeks there was substantial growth of the F. subglutinans (white mycelium in the right container). The ammonia level was 71.4 in the control on the left and 12.1 in the d container on the right.

Figure 6. The growth of various new isolates ofFusarz'um spp. as compared to the growth ofF. culmorum (P24) on human waste are shown here. The progressive growth of Fusarz'um spp on small s of human waste are shown here ca. 100 mg (fresh weight) over the course ofmany days. The growth of newly isolated and characterized Fusarz'um spp. are each compared to P2-24 which is Fusarz'um culmorum, the subject of a previous patent on this topic.

The new Fusarium spp. especially E06-1 and E06-5 do grow faster on the waste. Growth was measured from the extent of the mycelium moving out from the agar plug placed on the dollop of waste.

Figure 7. Top — A six day old culture ofFusarz'um subglutinans E06-1 the preferred fungus to be used to treat human and animal wastes in ation with System 2.Bottom a light microscopic view of spores and hyphae of F. subglutinans. The spores are slightly curved and are 9.8 -12 x 2.5u.

Figure 8. Fusarl'um subglutinans (E06-8) growing profusely on human waste in the ce of System 2. Please note the inhibition of bacterial growth to the right side of the culture plate which is influenced by the vapors of System 2 emanating from the bentonite particles on the left side of the plate allowing for fungal . There were 0.5 g of treated bentonite added, ca 100 mg of human waste and the plate had incubated for 12 days. See Figure 6 for comparative growth ements.

Method 1- Experimental procedure for isolating Fusarl'um spp endophy_tes Isolates ofFusarz'um spp. may be collected according to standard protocols understood by those skilled in the art. In brief, twig pieces were thoroughly soaked in 70% aqueous ethanol solution for e disinfection and then outer bark/epidermis was removed with sterile scalpel.

Small pieces of inner bark were aseptically transferred to the surface of water agar (WA) and glycerol- arginine medium (GAM). After tion for several days at 25 CC, hyphal tips of developing fungi should be aseptically removed and placed on potato dextrose agar (PDA). Pure fungal cultures were acquired in this manner. In particular isolates that have a pink to reddish coloration and possessing sickle shaped spores are likely to be endophytic Fusarium spp. Further characterization by molecular techniques can be made as understood by those skilled in the art.

This procedure was used to find each of the organisms used and bed herein.

Shown in Table l, are the inhibition and killing effects of propanoic acid, and isobutryic acid together and alone and with various esters. The tests were conducted over the course of 30 hr at 22 °C. Measurements were made on riate ls and thus the percentage of tion ations could be made on treatments vs the growth on a control organism (non- treated). The bacteria and yeast like organisms were evaluated on the basis of relative growth rates after 30 hr. Those highlighted areas on the table show those compounds (esters) having the most compatibility with propanoic and isobutryic acid l:l V/V mixtures with the appropriate esters at a 7:2 ratio- Systems 1 and 2 above. It is from this test that s 1 and 2 were discovered. The acids were added at 7ul individually and combination of the esters with the acids were added at the 9 ul level in the plate assay.

Table 1.

Test Organism Cercospora Phytophthora Verticz'llium Sclerotz'm'a Pythz’um Comoound tested ola cinnamomi dahll'ae sclerotiorum ultimum Control 0% 0% Isobutyric Acid + 95% 87% 70% Propan01c Ac1d yric Acid 100% Propanoic Acid 67% Ethyl Isobutyratc 95% 100% 80% ISOPTOPYI 95% —33% 96% Isobutyrate Isobutyl Isobutyratc 95% 92% Butyl Isobutyrate 95% 60% Isobutyl Butyrate 33% Isoamyl Butyratc 1 00% Isoamyl yrate 95% 96% Isobutyl Propionatc 100% 88% Isobutyl Acetate 95% 60% Propyl yrate 95% 88% Isobutyl Isovalerate 1 00% Fusarium Rhizoctom'a Aspergillus sub lutinans viria’ae solam' umz’; atus Control 0% 0% 0% Isobutyric Acid + 20% 86% 0% Propanoic Acid Isobutyric Acid Propanoic Acid Ethyl Isobutyratc Isopropyl Isobutyrate yl Isobutyrate Butyl Isobutyrate Isobutyl Butyrate Isoamyl Butyratc Isoamyl Isobutyrate Isobutyl Propionatc yl Acetate Propyl Isobutyrate Isobutyl Isovalcratc Saccharomyces Candida albicans Escherichia coli us subtilis cerevicae Control Growth Observed Growth Observed Growth Observed Growth Observed Isobutyric Acid + Growth Observed Inhibited Propanoic Acid Isobutyric Acid Growth Observed Growth Observed Propanoic Acid Growth Observed Growth Observed Ethyl Isobutyrate Growth Observed Growth Observed Isopropyl Growth Observed No Growth No Growth Growth Observed Isobutyrate yl Isobutyrate Growth Observed Inhibited Inhibited Growth Observed Butyl Isobutyrate Growth Observed Growth Observed yl Butyrate Growth Observed Growth Observed Isoamyl Butyrate No Growth Growth Observed Isoamyl Isobutyrate Growth Observed Growth Observed yl Propionate Growth Observed \0 Growth \0 Growth Growth Observed Isobutyl e Growth Observed ted Inhibited Growth Observed Propyl Isobutyrate Growth Observed Inhibited Inhibited Growth Observed yl Isovalerate Growth Observed Inhibited ted Growth Observed Note: when No Growth or 100 % inhibition is noted the organisms were dead and not able to be revived.

Shown in Table 2 is a description of the molecular genetics data (below) obtained on the new isolates of fusarium that were tested for their ability to degrade human wastes. Each of these isolates is so designated on the g. Details of the data acquisition are provided at the end of the table.

Table 2.

E 06-05 Fusarium subglutinans Sequence (480 bases): AACATACCAATTGTTGCCTCGGCGGATCAGCCCGCTCCCGGTAAAACGGGACGGCC CGCCAGAGGACCCCTAAACTCTGTTTCTATATGTAACTTCTGAGTAAAACCATAAAT AAATCAAAACTTTCAACAACGGATCTCTTGGTTCTGGCATCGATGAAGAACGCAGCA AAATGCGATAAGTAATGTGAATTGCAGAATTCAGTGAATCATCGAATCTTTGAACGC ACATTGCGCCCGCCAGTATTCTGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCT CAAGCCCAGCTTGGTGTTGGGACTCGCGAGTCAAATCGCGTTCCCCAAATTGATTGG CGGTCACGTCGAGCTTCCATAGCGTAGTAGTAAAACCCTCGTTACTGGTAATCGTCG CGGCCACGCCGTTAAACCCCAACTTCTGAATGTTGACCTCGGATCAGGTAGGAATAC CCGCTGAACTTAAGCATATCAATAA (SEQ ID NO: 1) NCBI BLAST Matches: Score Score Cover Value Ident Fusarium verticillioides voucher PF 14862 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and . KC709665.1 internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Fungal sp. AM20l3 strain l86_Jm internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and internal KC506334.l ribed spacer 2, te sequence; and 28S ribosomal RNA gene, partial Fusarium subglutinans strain Hl 18S ribosomal RNA gene, l sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and al . JX96043 l .l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial seuence Fusarium sacchari internal transcribed spacer 1, partial sequence; 5.8S ribosomal JN997445.l RNA gene and internal transcribed spacer 2, comolete seuence; and 28S ribosomal RNA ene, artial seuence Fusarium sp. PRE4b 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S mal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|KC254039.l| Gibberella intermedia culture-collection 887 0.0 JN254793.l UOA/HCPF<GRC>: l2610 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Gibberella moniliformis isolate FM2 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal JF499676.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l seuence Gibberella moniliformis genes for 18S rRNA, ITSl, 5.8S rRNA, ITS2, 28S rRNA, AB587012.l partial and complete sequence, strain: MAFF 240085 Gibberella moniliformis genes for 18S rRNA, ITSl, 5.8S rRNA, ITS2, 28S rRNA, AB587010.l partial and complete sequence, strain: CBS 576.78 um subglutinans genes for 18S rRNA, ITSl, 5.8S rRNA, ITS2, 28S rRNA, AB587008.l partial and complete ce, strain: ATCC 38016 Gibberella moniliformis strain Gm3 18S ribosomal RNA gene, partial sequence; al transcribed spacer l, 5.8S ribosomal RNA gene, and al HQ718417.1 ribed spacer 2, complete ce; and 28S ribosomal RNA gene, l seuence E 06-08 um subglutinans Sequence (478 bases): CATACCAATTGTTGCCTCGGCGGATCAGCCCGCTCCCGGTAAAACGGGACGGCCCG CCAGAGGACCCCTAAACTCTGTTTCTATATGTAACTTCTGAGTAAAACCATAAATAA ATCAAAACTTTCAACAACGGATCTCTTGGTTCTGGCATCGATGAAGAACGCAGCAAA ATGCGATAAGTAATGTGAATTGCAGAATTCAGTGAATCATCGAATCTTTGAACGCAC ATTGCGCCCGCCAGTATTCTGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCTCA AGCCCAGCTTGGTGTTGGGACTCGCGAGTCAAATCGCGTTCCCCAAATTGATTGGCG TCGAGCTTCCATAGCGTAGTAGTAAAACCCTCGTTACTGGTAATCGTCGCG GCCACGCCGTTAAACCCCAACTTCTGAATGTTGACCTCGGATCAGGTAGGAATACCC GCTGAACTTAAGCATATCAATAA (SEQ ID NO: 2) NCBI BLAST Matches: Description —otal Query_coreScore Accession Cover Fusarium verticillioides voucher UOA/HCPF 14862 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and . KC709665.1 internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, . artial se a uence Fungal sp. AM2013 strain 186_Jm internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and KC506334.1 internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, . artial se a uence Fungal sp. AM2013 strain 165_Gbp al ribed spacer 1, partial ce; 5.8S ribosomal RNA gene and KC506316.1 internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, . artial se a uence Fusarium subglutinans strain H1 18S ribosomal RNA gene, partial sequence; al transcribed spacer 1, 5.8S ribosomal RNA gene, and internal 883 883 100% 0.0 100% JX960431.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Fusarium sacchari internal transcribed spacer 1, partial sequence; 5.8S ribosomal R\IA gene and internal transcribed spacer 883 883 100% 0.0 100% JN997445.l 2, complete sequence; and 28S ribosomal R\IA ene, . artial se a uence Gibberella moniliformis isolate FMll internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and HQ995666.l internal transcribed spacer 2, te sequence; and 28S ribosomal RNA gene, . artial se a uence Fusarium sp. PRE4b 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S mal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|KC254039.l| Gibberella intermedia culture-collection JN254793.l UOA/HCPF<GRC>: 12610 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, te sequence; and 28S mal RNA ene, artial seuence ella moniliformis isolate FM2 18S ribosomal RNA gene, partial sequence; internal ribed spacer l, 5.8S ribosomal RNA gene, and internal JF499676.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial seuence Gibberella moniliformis genes for 18S rR\IA, ITSl, 5.8S rRNA, ITS2, 28S 12.l rR\IA, partial and complete sequence, strain: MAFF 240085 ella formis genes for 18S rR\IA, ITSl, 5.8S rRNA, ITS2, 28S 883 883 100% 0.0 100% AB587010.l rR\IA, partial and complete sequence, strain: CBS 576.78 E 4 -5 Fusarium sp.

Sequence (488 bases): CTTAATGTTGCCTCGGCGGATCAGCCCGCGCCCCGTAAAACGGGACGGCCCGCCAG AGGACCCAAACTCTAATGTTTCTTATTGTAACTTCTGAGTAAAACAAACAAATAAAT CAAAACTTTCAACAACGGATCTCTTGGTTCTGGCATCGATGAAGAACGCAGCAAAAT GCGATAAGTAATGTGAATTGCAGAATTCAGTGAATCATCGAATCTTTGAACGCACAT TGCGCCCGCTGGTATTCCGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCTCAAG CCCCCGGGTTTGGTGTTGGGGATCGGCTCTGCCTTCTGGCGGTGCCGCCCCCGAAAT ACATTGGCGGTCTCGCTGCAGCCTCCATTGCGTAGTAGCTAACACCTCGCAACTGGA ACGCGGCGCGGCCATGCCGTAAAACCCCAACTTCTGAATGTTGACCTCGGATCAGGT AGGAATACCCGCTGAACTTAAGCATATCAATAG (SEQ ID NO: 3) NCBI BLAST Matches: Description Max Total Query E Max Accession Score Score Cover Value Ident Uncultured um clone R1_12 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal KC753424.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial seuence Uncultured Fusarium genomic DNA containing 18S rRNA gene, ITSl, 5.8S HE977525.l rRNA gene, ITS2 and 28S rRNA gene, clone RRAl 0 Fusarium ctum isolate XSCZ07 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and JQ676180.l internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, . artial se a uence Uncultured fungus clone Hypl2 internal transcribed spacer 1, partial sequence; .8S ribosomal RNA gene and internal JQ6l8507.l ribed spacer 2, complete ce; and 28S ribosomal RNA gene, partial seuence Fusarium tricinctum e UASWS0796 18S mal RNA gene, internal transcribed spacer l, 5.8S ribosomal RNA 900 900 99% 0.0 100% JN662408.l gene, internal ribed spacer 2, and 28S ribosomal RNA gene, region Fusarium sp. NRRL 52933 internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal ribed spacer 2, 900 900 99% 0.0 100% JF740937.l complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium sp. NRRL 527l4 internal transcribed spacer l, 5.88 ribosomal RNA gene, and al transcribed spacer 2, JF7409ll.l complete sequence; and 28S ribosomal RNA gene, partial sequence Fusarium sp. NRRL 25 129 al transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence 7409l6. l| Fusarium sp. NRRL 52726 internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete ce; and 28S ribosomal RNA gene, partial sequence >gb|JF7409l7.l| Fusarium sp. JF740895.l NRRL 52727 internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|JF7409l8.l| um sp.

NRRL 52730 internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial seuence um sp. NRRL 25128 internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, JF740894.l complete ce; and 28S ribosomal RNA ene, artial seuence Gibberella avenacea isolate 3214 188 ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal FJ224099.l transcribed spacer 2, complete ce; and 28S ribosomal RNA gene, partial seuence PC24 (Control) Fusarium um Sequence (477 bases): CATACCTTATGTTGCCTCGGCGGATCAGCCCGCGCCCCGTAAAAAGGGACGGCCCG CCGCAGGAACCCTAAACTCTGTTTTTAGTGGAACTTCTGAGTATAAAAAACAAATAA ATCAAAACTTTCAACAACGGATCTCTTGGTTCTGGCATCGATGAAGAACGCAGCAAA ATGCGATAAGTAATGTGAATTGCAGAATTCAGTGAATCATCGAATCTTTGAACGCAC ATTGCGCCCGCCAGTATTCTGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCTCA AGCCCAGCTTGGTGTTGGGAGCTGCAGTCCTGCTGCACTCCCCAAATACATTGGCGG TCACGTCGAGCTTCCATAGCGTAGTAATTTACATATCGTTACTGGTAATCGTCGCGG CGTTAAACCCCAACTTCTGAATGTTGACCTCGGATCAGGTAGGAATACCCG CTGAACTTAAGCATATCAATAG (SEQ ID NO: 4) NCBI BLAST Matches: Description Total Query Accession Score Score Cover Fusarium sp. OTU930 internal transcribed spacer 1, partial sequence; 5.8S ribosoma1 R\IA gene and internal transcribed spacer GU934527.1 2, complete sequence; and 28S ribosomal R\IA ene,artia1- seuence Fusarium culmorum isolate 149 18S ribosomal RNA gene, partial sequence; al transcribed spacer 1, 5.8S ribosomal RNA gene, and internal 94.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l seuence Fusarium cerea1is genes for contains 18S rRNA, ITS1, 5.8S rRNA, ITS2, 28S rRNA, partial and complete sequence, ' AB820718'1 strain: MAFF 101 144 Fusarium culmorum genes for 18S rRNA, ITS1, 5.8S rRNA, ITS2, 28S rRNA, partial and te sequence, strain: MAFF 241212 >dbj|AB820717.1| AB586990.1 Fusarium cerea1is genes for ns 18S rRNA, ITS1, 5.8S rRNA, ITS2, 28S rRNA, partial and complete sequence, strain: MAFF 241212 um cerea1is strain FC3 18S ribosomal RNA gene, internal transcribed spacer 1, 5.8S ribosomal RNA gene, JF303876.1 internal transcribed spacer 2, and 28S ribosomal RNA _ene, re ion um cerealis strain FC2 l8S ribosomal RNA gene, internal transcribed spacer l, 5.88 ribosomal RNA gene, 880 880 99% 0.0 100% JF30387l.l internal transcribed spacer 2, and 28S ribosomal RNA _ene, re - ion Fusarium cerealis strain FCl l8S ribosomal RNA gene, internal transcribed spacer l, 5.88 ribosomal RNA gene, JF303867.l internal transcribed spacer 2, and 28S ribosomal RNA gene, region Fusarium culmorum strain G5 188 ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 mal RNA gene, and internal GU56627l .l transcribed spacer 2, complete ce; and 28S ribosomal RNA gene, partial seuence Uncultured Hypocreales clone B2_i_ITS lF al transcribed spacer 1, partial sequence; 5.8S ribosomal RNA EU754930.l gene, complete ce; and internal transcribed s.acer 2, oartial seuence Uncultured Hypocreales clone B3_l_c_ITS lF internal transcribed spacer 1, partial sequence; 5.8S mal RNA EU754928.l gene, complete sequence; and internal transcribed s.acer 2, oartial seuence E 30 -14 Fusarium avenaceum Sequence (485 bases): CAGAAGTTGGGGTTTTACGGCATGGCCGCGCCGCGTTCCAGTTGCGAGGTGTTAGCT ACTACGCAATGGAGGCTGCAGCGAGACCGCCAATGTATTTCGGGGGCGGCACCGCC AGAAGGCAGAGCCGATCCCCAACACCAAACCCGGGGGCTTGAGGGTTGAAATGACG CTCGAACAGGCATGCCCGCCGGAATACCAGCGGGCGCAATGTGCGTTCAAAGATTC GATGATTCACTGAATTCTGCAATTCACATTACTTATCGCATTTTGCTGCGTTCTTCAT CGATGCCAGAACCAAGAGATCCGTTGTTGAAAGTTTTGATTTATTTGTTTGTTTTACT CAGAAGTTACAATAAGAAACATTAGAGTTTGGGTCCTCTGGCGGGCCGTCCCGTTTT ACGGGGCGCGGGCTGATCCGCCGAGGCAACATTAAGGTATGTTCACAGGGGTTTGG TAAACTCGGTAATGATCCCTCCGCA (SEQ ID NO: 5) NCBI BLAST s: E Max Accession Score Score Cover Value Ident Fusarium avenaceum 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, JX402l84.l complete sequence; and 28S mal RNA gene, partial sequence > b JX402l87.l Fusarium avenaceum 18S ribosomal RNA gene, l sequence; internal transcribed spacer l, 5.8S ribosomal RNA JX402l83.l gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial e Fusarium avenaceum 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA JX402l80.l gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium avenaceum 18S ribosomal RNA gene, l sequence; internal transcribed spacer l, 5.8S ribosomal RNA JX402l79.l gene, and al transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium tricinctum strain wxm38 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal 896 896 100% 0.0 100% HM037940.l transcribed spacer 2, complete sequence; and 28S mal RNA gene, partial seuence Fusarium tricinctum genes for 188 rRNA, ITSl, 5.8S rRNA, ITS2, 28S rRNA, AB470855.l partial and complete ce, isolate: TSO82 Fusarium tricinctum genes for 188 rRNA, ITSl, 5.8S rRNA, ITS2, 28S rRNA, partial and complete sequence, isolate: TSO8l >dbj|AB4708l8.l| Fusarium tricinctum genes for 188 rRNA, ITSl, .8S rRNA, ITS2, 28S rRNA, l and complete ce, isolate: TSO8l AB470859.l >gb|GU586834. l| Fusarium tricinctum isolate pr30 188 mal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, . artial se a uence Gibberella avenacea isolate FA37 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal FJ602983.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l seuence Gibberella ea isolate FAl8 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l sequence >gb|FJ602975.l| Gibberella FJ602964.l avenacea isolate FA29 l8S ribosomal RNA gene, partial ce; internal transcribed spacer l, 5.88 ribosomal RNA gene, and al transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence > b FJ603000.l Gibberella avenacea isolate FA54 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA gene, partial sequence Gibberella avenacea e FAl7 l8S ribosomal RNA gene, l ce; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA gene, partial sequence >gb|FJ602968. l| Gibberella avenacea e FA22 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|FJ602973 . l | Gibberella ea isolate FA27 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and 896 896 100% 0.0 100% FJ602963.l al ribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|FJ60298 l . l| Gibberella avenacea isolate FA35 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA gene, partial sequence >gb|FJ602999. l| Gibberella avenacea isolate FA53 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence E 06-7 Fusarium tinans Sequence (469 : CAGAAGTTGGGGTTTAACGGCGTGGCCGCGACGATTACCAGTAACGAGGGTTTTACT ACTACGCTATGGAAGCTCGACGTGACCGCCAATCAATTTGGGGAACGCGATTTGACT CGCGAGTCCCAACACCAAGCTGGGCTTGAGGGTTGAAATGACGCTCGAACAGGCAT GCCCGCCAGAATACTGGCGGGCGCAATGTGCGTTCAAAGATTCGATGATTCACTGA ATTCTGCAATTCACATTACTTATCGCATTTTGCTGCGTTCTTCATCGATGCCAGAACC AAGAGATCCGTTGTTGAAAGTTTTGATTTATTTATGGTTTTACTCAGAAGTTACATAT AGAAACAGAGTTTAGGGGTCCTCTGGCGGGCCGTCCCGTTTTACCGGGAGCGGGCT GATCCGCCGAGGCAACAATTGGTATGTTCACAGGGGTTTGGGAGTTGTAAACTCGGT AATGATCCCTCCGC (SEQ ID NO: 6) NCBI BLAST Matches: Score Score Cover Value Ident Fusarium verticillioides r UOA/HCPF 14862 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosoma1 100% I 100% KC709665. 1 RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence um subg1utinans strain AAFCFcir-012 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, 867 867 100% 100% KC464632.1 and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibbere11a moni1iformis genomic DNA n1ng 18S rRNA gene, ITS1, 5.8S 867 100% 100% HF570008.1 rRNA gene, ITS2 and 28S rRNA gene, strain DBT-112 Gibbere11a formis isolate SIDV20110221051 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosoma1 867 100% 100% KC143121.1 RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibberella intermedia r LFG4- 3BBRS internal transcribed spacer l, .88 ribosomal RNA gene, and internal 867 867 0.0 JQ272470.1 transcribed spacer 2-like gene, partial se a uence; ondrial Gibberella moniliformis strain CBl l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal JXSll973.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Fusarium sp. CHTAG40 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal JF773630.l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium sp. CHTAG38 l8S mal RNA gene, partial sequence; internal ribed spacer l, 5.88 mal JF773629.l RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA ene, artial e Fusarium sp. CHTAG34 l8S ribosomal RNA gene, partial ce; internal transcribed spacer l, 5.88 ribosomal JF773628.l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium sp. CHTAG32 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal JF773627.l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence WO 03082 E-30 -7 Fusarium avenaceum Sequence (480 bases): GAAGTTGGGGTTTTACGGCATGGCCGCGCCGCGTTCCAGTTGCGAGGTGTTAGCTAC TACGCAATGGAGGCTGCAGCGAGACCGCCAATGTATTTCGGGGGCGGCACCGCCAG AAGGCAGAGCCGATCCCCAACACCAAACCCGGGGGCTTGAGGGTTGAAATGACGCT CGAACAGGCATGCCCGCCGGAATACCAGCGGGCGCAATGTGCGTTCAAAGATTCGA TGATTCACTGAATTCTGCAATTCACATTACTTATCGCATTTTGCTGCGTTCTTCATCG ATGCCAGAACCAAGAGATCCGTTGTTGAAAGTTTTGATTTATTTGTTTGTTTTACTCA ACAATAAGAAACATTAGAGTTTGGGTCCTCTGGCGGGCCGTCCCGTTTTAC GGGGCGCGGGCTGATCCGCCGAGGCAACATTAAGGTATGTTCACAGGGGTTTGGGA GTTGTAAACTCGGTAATGATCCCTCC (SEQ ID NO: 7) NCBI BLAST s: Description Max Total Query E Max Accession Score Score Cover Value Ident Fusarium avenaceum e 143 18S mal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal 887 100% 100% KC989099.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Uncultured Fusarium clone R1_12 18S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.8S ribosomal RNA gene, and internal 887 100% 100% KC753424.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium avenaceum strain Fkl 5 small subunit ribosomal RNA gene, partial sequence; internal transcribed spacer l, .8S ribosomal RNA gene, and internal 887 100% 100% KC464345.1 transcribed spacer 2, complete sequence; and large t ribosomal RNA ene, artial seuence Fusarium avenaceum l8S ribosomal RNA gene, l sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|JX402l87.l| Fusarium avenaceum l8S ribosomal RNA gene, partial sequence; al transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l sequence >gb|JX402l88.l| Fusarium avenaceum l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, 887 887 100% 0.0 100% JX402l84.l and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|JX402l89.l| Fusarium avenaceum l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l ce >gb|JX402l90. 1| Fusarium avenaceum l8S mal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA gene, partial sequence Fusarium avenaceum l8S ribosomal RNA gene, partial sequence; al transcribed spacer l, 5.88 ribosomal 887 887 100% 0.0 100% JX402l83.l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l sequence um avenaceum l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal 887 887 100% 0.0 100% JX402l80.l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Fusarium avenaceum l8S ribosomal RNA gene, l sequence; internal transcribed spacer l, 5.88 ribosomal 887 887 100% 0.0 100% JX402l79.l RNA gene, and internal transcribed spacer 2, complete ce; and 28S ribosomal RNA gene, partial sequence Uncultured Fusarium genomic DNA containing 188 rRNA gene, ITSl, 5.8S 887 887 100% 0.0 100% HE977545.l rRNA gene, ITS2 and 28S rRNA gene, clone RRFOl Fusarium sp. CHTAM47 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal 887 887 100% 0.0 100% JF773662.l RNA gene, and al transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Fusarium sp. CHTAM2 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal 887 887 100% 100% JF773634.l RNA gene, and internal ribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence E 06-01 Fusarium subglutinans Sequence (468 : GAAGTTGGGGTTTAACGGCGTGGCCGCGACGATTACCAGTAACGAGGGTTTTACTAC TACGCTATGGAAGCTCGACGTGACCGCCAATCAATTTGGGGAACGCGATTTGACTCG CGAGTCCCAACACCAAGCTGGGCTTGAGGGTTGAAATGACGCTCGAACAGGCATGC CCGCCAGAATACTGGCGGGCGCAATGTGCGTTCAAAGATTCGATGATTCACTGAATT CTGCAATTCACATTACTTATCGCATTTTGCTGCGTTCTTCATCGATGCCAGAACCAAG AGATCCGTTGTTGAAAGTTTTGATTTATTTATGGTTTTACTCAGAAGTTACATATAGA AACAGAGTTTAGGGGTCCTCTGGCGGGCCGTCCCGTTTTACCGGGAGCGGGCTGATC CGCCGAGGCAACAATTGGTATGTTCACAGGGGTTTGGGAGTTGTAAACTCGGTAATG ATCCCTCCGCA (SEQ ID NO: 8) NCBI BLAST Matches: Description Max Total Query Max Accession Score Score Cover Ident um verticillioides voucher UOA/HCPF 14862 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal KC709665 . l RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibberella moniliformis c DNA containing 18S rRNA gene, ITS1, 5.8S HF570008.1 rRNA gene, ITS2 and 28S rRNA gene, strain DBT-112 Gibberella moniliformis isolate SIDV20110221051 18S mal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal 865 KC 143 121 . 1 RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibberella moniliformis strain CB1 18S ribosomal RNA gene, partial ce; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal JXS l 1973 .1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence ella moniliformis isolate FM13 18S ribosomal RNA gene, l HQ995667.1 sequence; internal transcribed spacer 1, .8S ribosomal RNA ene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibberella moniliformis isolate FM2 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, .88 ribosomal RNA gene, and internal JF499676.l transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence Fusarium sp. Ljf001 l8S ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal HQ025928.1 RNA gene, and internal transcribed spacer 2, te sequence; and 28S ribosomal RNA ene, artial seuence Gibberella sp. FLS-2010 isolate FS- 74(3) 188 ribosomal RNA gene, partial sequence; internal transcribed spacer l, .88 mal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, l sequence >gb|HQ0232l4. l| Gibberella sp. FLS-2010 isolate FS-78(3) l8S mal RNA gene, partial sequence; internal transcribed spacer l, 5.88 ribosomal RNA gene, and internal HQ023213.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence >gb|HQ0232 l 5. 1| illus sp. FLS-20lO isolate FS-55(3) l8S ribosomal RNA gene, partial sequence; internal ribed spacer l, 5.88 ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence Gibberella sp. 10 isolate FS- 485(1) 188 ribosomal RNA gene, partial sequence; internal transcribed spacer l, 5.88 mal RNA gene, ll.l and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial seuence WO 03082 Gibberella sp. FLS-2010 isolate FS- 82(3) 18S mal RNA gene, partial sequence; internal transcribed spacer 1, .8S ribosomal RNA gene, and internal 865 865 100% 0.0 100% HQ023203.1 transcribed spacer 2, complete sequence; and 28S ribosomal RNA ene, artial se uence ITS based phylogenetic analysis Phylogenetic analysis of these organisms was d out by the ition of the ITS- .8 S ribosomal gene sequence. The fungus was grown on PDA for 7 days and DNA templates were prepared by using the Prepman Ultra Sample Preparation Reagent (Applied Biosystems, USA) according to the manufacturer’s guidelines. The ITS regions of the fungus were amplified with the universal ITS primers ITSl (5’ TCCGTAGGTGAACCTGCGG 3’; SEQ ID NO: 9) and ITS4 (5’TCCTCCGCTTATTGATATGC 3’; SEQ ID NO: 10) using Polymerase Chain Reaction (PCR). The PCR conditions used were as follows: initial denaturation at 94°C for 3 min followed by 30 cycles of 94°C for 15 sec., 50°C for 30 sec., 72°C for 45 sec., and a final extension at 72°C for 5 min. The 50 ul reaction e contained 1x PCR , 200 pM each dNTP, 1.5 mM MgC12, 10 pmol of each primer, 1—5 ng ofDNA and 2.5 U of Taq DNA polymerase. The amplified product (5 ul) was visualized on 1% (w/v) agarose gel to confirm the ce of a single amplified band. The amplified products were purified by Amicon Ultra columns (Millipore, USA) and 20—40 ng were used in a 10 ul sequencing reaction using the Big Dye Terminator sequencing kit (V. 3.1), with 2 pmoles of the forward or the e primer in the cycle sequencing reaction. Twenty cycles of 96 °C for 10 s, 50 °C for 5 s and 60 °C for 4 min were performed and the extension products were purified by ethanol precipitation, dissolved in ul of HiDi Formamide, incubated at 95 °C for 1 min and loaded on ABI Prism 377 Genetic Analyzer (Perkin-Elmer, USA) for sequencing. All the reagents for sequencing were from Applied Biosystems, USA. The amplified products were sequenced and aligned with the ces in the GenBank by BLASTN program hul et al., 1997). Sequencing was performed at the U Calif, Berkeley.

Shown in Table 3 is the growth of s fusaria on human wastes causes a reduction of the dry weight of the mass during the course of a 7 week experiment. The experimental set- up contained 0.5 g of bentonite with System 2 on a water agar plate having about 100 mg wet weight of human waste and a small agar plug with the test fusarium on it. The incubation period was 7 weeks at 22 °C. The remains of the human waste were physically removed and dried for 4 hr at 80 °C and then weighed.

Table 3.

Fusarium isolate designation Dry weight of the human waste remaining after 7 weeks. mg.

Control- no fusarium EC--45 E06-7 P2-24 Fusarium culmorum Original control Example 2 Establishment 0fS—3 and S—4 mixes Tests were conducted as similarly bed for Systems 1 and 2 above (Figure 9) to ascertain the biological actiVities of various test mixtures against a panel of test microbes. A small plug of each organism was placed in the periphery of the PDA plate. In the center well was placed the test solution in the plastic cup holder. A control plate (A) was also setup. After 30 hr the growth of the test organisms was compared to that of the l and the % inhibition was ated. The (B) plate contained the test e. ements were made 30 hr after plate set up.

It is to be noted that the System 1 and 2 mixtures described herein contain about 3.5 parts of propanoic acid along with 3.5 parts of isobutryic acid and finally two parts of an ester- either isoamyl butryate (System 1) or isoamyl isobutryate (System 2). It is realized that while these mixtures are effective in a number of applications there may be other mixtures that are even more effective by virtue of their range of biological activities, their utility and their effectiveness at low doses. To this end, a search was conducted using the standard propanoic acid as a starting point whilst omitting isobutryic acid (because of its offensive odor) and now including larger molecular weight esters as the ester component. Quite singly and ctedly, it was discovered that the use of propanoic acid (7) parts and Isoamyl Hexonates (2) parts produced a volatile mixture with biological activities that exceeded that of either B-23 (see below), and S-l as shown in Table 4. This new mixture is designated as System 3, while the formulation comprising propanoic acid (7) and formate (2) is ated System 4. It is to be noted that System 4 is less active t most of the test organisms than System 3, but System 4 does kill E coli while allowing for the growth of Fusarium. To this end, System 4 is an effective e to be used as a human waste treatment along with Fusarium spp.

Table 4. The effects of various esters and propanoic acid on the growth of test organisms measured at 30 hr at room temperature. The effect is ented as percent inhibition of the growth when directly compared to the growth of an uninoculated control. Measurements (average of two) were made as the hyphal growth from the edge of the inoculum plug.

Cercospora Phytophthora Verticillium Sclerotinia Pythium beticola cinnamomi dahliae tiorum ultimum '1 3011““ 100 72 92 0 100 Propanoic Acid Propanoic Acid with Isoamyl Propanoic Acid with Isobutyl Propanoic Acid with Isoamyl Hexonates (7:2) = S-3 * Propanoic Acid 100 92 100 2014/045297 with Isoamyl Formate & c Propanoic Acid with equal mix of formatcs & valenccnc Propanoic Acid with equal mix of 98 92 100 64 100 formatcs (7:2) Propanoic Acid with Hexyl Formate 100 8 8 87 60 100 (7 :2 :) Fusariurn Trichoderma Rhizoctonia Aspcrgillus solani Viridac flavus S-l on B-23** Isoarnyl chonatcs 2 l Propanoic Acid Propanoic Acid with Isoamyl Formatc 7:2 = S-4 Propanoic Acid with Isobutyl Formatc (7:2) Propanoic Acid with Isoamyl Hexonatcs (7:2)= S- 3>l< Propanoic Acid with Isoamyl Formate & Cincolc oic Acid with equal mix of 74 35 77 43 formatcs & valenccnc (7:2:0.5) Propanoic Acid with equal mix of 58 30 77 29 formatcs 7:2 Propanoic Acid with chyl Formatc 7 :2: Activity against yeasts and bacteria Yes = Growth Medium = Some Growth N0 = No Growth Candida Escherichia Bacillus Saccharomyces albicans coli us cereviceae S-l Solution Some growth No No Yes Isloamyl Hexonates (2 Yes Yes Yes Yes Propanoic Acid Yes Propanoic Acid with Isoamyl Formate (7:2) Yes Propanoic Acid with Isobutyl Formate (7:2) Propanoic Acid with Isoamyl Hexonates (7:2) S-3 * Propanoic Acid with Isoamyl Formate & Cineole (7:l:l) oic Acid with equal mix of formates & ene (7:2:0.5) oic Acid with equal mix of formates Propanoic Acid with Hex lFormate 7:2: * S-3 tests were run for 30 hr at room temp and then measured and photographed. Measurements made from edge of inoculation block to edge of colony. Two measurements made and then averaged. The tests were run at room temp.

The results show that S-3 was the most biological active mixture of the solutions tested. Also Note S3 , Inhibiting Erwinia carotovora: 80 2 90% and inhibiting Lactobacillus sp. ca. 50%.

** B-23 a tested is as follows: 1.39 parts acetaldehyde; 2.83 parts 2-butanone; 30.56 parts propanoic acid, 2- methyl-,methyl ester; 2.29 parts acetic acid, 2-methylpropyl ester; 1.09 parts propanoic acid, 2-methyl-, 2- methylpropyl ester; 1.78 parts 1-propanol, 2-methyl-; 1.51 parts 2-butenal, 2-methyl-, (E)-; 4.79 parts nol, 3- methyl-, acetate; 4.78 parts propanoic acid, 2-methyl-, 2-methylbutyl ester; 5.38 parts nol, 3-methyl-; 351.18 parts propanoic acid, 2-methyl-; 1.31 parts acetic acid, 2-phenylethyl ester.

It is to be noted that the 8-3 mixture gave 100 % inhibition to many of the sms tested (Table 4). The effect was greater than with Isoamyl Hexonatess or propanoic acid alone.

Thus in some cases it appeared to be strongly synergistic ie. Sclerotina tiorum 66 % with hexanoates, 0% with propanoic and 100% when the two were combined. Some other sms also reacted in the same manner such as Rhizoctonia solani. In addition it appeared that 8-3 was more active than 8-1, as well as B-23 and of course the Isoamyl tes or propanoic acid alone (Table 4). Other combinations of propanoic acid and other esters or combinations of esters and oids such as cineole or ene were not as effective (Table 4). The 8-4 formulation, although not as active as 8-3, did not cause such a great effect on Fusarium but it was inhibitory to other microbes and thus it may be best suited as a useful agent in to treat human wastes in combination with the Fusarium. S-3 did kill both bacterial test organisms in the tests (Table 4).

S-3 also affected Erwinia and Lactobacillus sp. (Table 4).

Establishment 0fthe appropriate ratios ofingredientsfor 5-3 The mixes of propanoic acid to Isoamyl Hexonates were varied and subsequently tested according to the procedures outlined above. It turns out that the most favorable mixture was the 7:2 ratio of the two ingredients (Table 5). All others gave lower inhibition values (Table 5). The addition of terpenoids such as valencene did not promote biological activity. Thus, the ratio of 7:2 V/V of the two ingredients is the most preferred for cal application.

Table 5. Effects of various ratios of propanoic acid to Isoamyl Hexonates on a panel of test ms. All tests were carried out as described in Table 4. beticola cinnamomi dahliae sclerotiorum ultimum Propanoic Acid with Isoamyl 100 100 100 100 Hexonates (7:2) = Propanoic Acid with Isoamyl Hexonates (5:4) Propanoic Acid with Isoamyl Hexonates Propanoic Acid with Isoarnyl Hexonates & Valencene 6:2:1 Fusarium Trichoderrna Rhizoctonia Aspergillus solani e solani flavus Propanoic Acid with Isoarnyl tes 7:2 Propanoic Acid with Isoarnyl Hexonates 5:4 oic Acid with Isoarnyl Hexonates 3 :6 Propanoic Acid with yl 72 59 93 50 Hexonates & Valencene (6:2: 1) Yes = Growth Medium = Sorne Growth N0 = No Growth Candida Escherichia Bacillus Saccharornyces albicans coli subtilus cereViceae Propanoic Acid with Isoarnyl Yes No Hexonates (7:2) Propanoic Acid with Isoarnyl Yes Trace Hexonates 5:4 Propanoic Acid Hexonates : Propanoic Acid ‘vailolsggsng Yes Some No Sorne Valencene 6:2:1 C. Testing of Other Esters with Propanoic acid As shown in Table 6 below, alternative esters were tested for mixture with propanoic acid at a ratio of 7:2 propanoic acid:ester. These formulations are in addition to formulations S-l, S- 2, S-3 and 8-4, and accordingly form part of the formulations of the present invention. It should also be iated that the present ion may include multiple esters or combinations of any of the esters bed hereinthroughout, in conjunction with propanoic acid, preferably at a ratio of 7:2 propanoic acid:ester mixture.

Table 6. Testing of Esters B. C. D. E.

Cercospora Phytophthora Verticillium Sclerotinia m beticola Cinnamomi* dahliae sclerotiorum ultimum Test solution Propanoic acid with Isoamyl benzoate (7:2) oic acid with Isoamyl phenylacetate (7:2) Propanoic acid with isoamyl cinnamate Propanoic acid with Isoamyl octanoate Propanoic acid with Isoamyl salicylate Propanoic acid with Isoam l laurate 7:2 sm not available F. G. H. I.

Fusariurn Trichodcrma Rhizoctonia Aspcrgillus solani Viridac solani flavus Propanoic acid with Isoarnyl tc (7:2) Propanoic acid with Isoarnyl acctatc (7:2) Propanoic acid with isoarnyl cinnamatc Propanoic acid with Isoarnyl octanoatc Propanoic acid with Isoarnyl salicylatc Propanoic acid with Isoarnyl Yes = Growth Medium = Sornc Growth N0 = No Growth Lactobacillus Erwinia C. Bacillus S_ carotovora albicans E. coli subtilus ccrcViccac Propanoic acid with Isoarnyl benzoatc (7:2) Propanoic acid with Isoarnyl ohcn lacctatc Propanoic acid with yl atc Propanoic acid with Isoarnyl octanoatc (7:2) Propanoic acid with Isoarnyl salicylatc Propanoic acid with lsoamyl laurate (7 :2) ‘ ‘ Control Yes Yes Yes Yes Yes Yes All testing was done according to the methods in Table 4 Example 3 Corn Decontamination tests Corn is fermented to make ethanol. It is ground, heated to a mash and treated with enzymes prior to the on of yeast cells to make a final preparation. Also added are one or more antibiotic preparations that tend to suppress otherwise competing microbes that would foul the fermentation process. As such antibiotics are being removed from the market place, other antimicrobial treatment processes are needful. To determine if the 8-3 preparation has cy against corn contaminating microbes the following was done: Approximately 5 g of ground corn (cracked com) was treated for 1 hr with 10 ml of 0% (control), 0.25 %, 0.5 % and 1% solutions of 8-3 made with 7:2 v/v plus 10 microliters of triton— x 100 (per 10 ml). The treatment was for 1 hr and the product was damp dried on paper tissue to remove excess liquid. About 2 grams of al was placed directly on a PDA plate and incubated for 2 days prior to being photographed. In another case, the cracked seed was dried under a hood and then plated on PDA.

The results trated that the treatment levels of 0.5% and 1.0 % 8-3 for 1 hr completely d the ial contamination of the cracked corn particles (Fig. 10). When the com particles were blotted dry and further dried and tested in the same manner, the results were virtually the same. l, the results indicate that the 8-3 solution can be used to decontaminate agriculturally and food based products and materials. This would likewise apply to instruments, equipment, clothing and food being processed for consumption.

Example 4 Use 0fS—4 in treatment ofhuman waste with Fusarium tinans.

Testing of formulae S-3 and 8-4 was done to learn of their efficacy in treating human waste ia. The testing was done using 0.5 g of bentonite having a rate of 1 ml 8-1, 8-2, 8-3 or S-4 or B-23 per 10 g of bentonite. The l was no mixture of compounds. Barley seeds contaminated with Fusarium subglutinans (same one as previously used) were placed on PDA plates. The mid plate was streaked with a pure culture of E coli obtained from human waste. Cap and seal with parafilm and then incubate for 3 days and raph. The S-3 and S-4 killed the E coli but there was less effect with B-23. The fusarium grew in the presence of S-3 and better with S-4. The E coli grew in the control and slightly in the presence of B-23 all as illustrated in Fig. 11. It is to be noted that S-4 in ite resulted in complete killing of E coli and the growth of the Fusarium did occur. This was also true of the S-1 and S-3 treatments but the Fusarium was more inhibited. The B-23 as a l was also effective in killing E. coli but not to the same degree. The results show that the S-4 is a good and reasonable treatment of human wastes to kill enteric bacteria with the concomitant use of Fusarium to allow for the breakdown of human waste als.

Example 5 Treatment of animal wastes with S-3 S-3 was applied at the rate of 3 ml per lb (0.45 kg) of zeolite. To test its efficacy in treating animal wastes with control of bacterial growth the following experiments were done.

The treated zeolite (0.5g) was placed in a center well of a PDA plate (cut out). The plate had been completely streaked and covered with a suspension of bacterial cells made from n, goat, cat and horse manure. The plates were covered and sealed with parafilm and then observed after 3 -4 days of tion and photographed. The results in all cases showed that the S-3 was an effective crobial mixture by virtue of the zone of inhibition that it caused on the plates.

This effect was also noted with the case of horse, goat and cat fecal matter bacteria spread on the plates (Fig. 12). The results suggest that the S-3 zeolite combination has the potential to be used as a cat litter treatment or a treatment for chicken coops or as an animal bedding application.

Example 6 The cy of S-3 as a cat litter treatment and as an animal bedding treatment was further tested.

Cat Litter Treatment Comparative Efficacy Testing A 1 ft.2 (0.09 m2) plastic snap-seal-top container was filled with the desired litter ent plus untreated bentonite in the proportions indicated by the packaging instructions (Figure 13). For these tests, CLOE (used at the rate of 4 ml per lb (0.45 kg)) and an untreated bentonite control were . A constant temperature was maintained in the testing facility for the duration of the tests (e.g. 70°F (21°C)). About 50 g of cat feces and 5 mL urine were added to treated containers. At 24 hour intervals, the ammonia level was measured in each box using the Z-800 ammonia meter. The measurements were done by placing the meter inside each box at respective 5-minute intervals, minimizing the amount of time the container spent open. The ammonia meter yielded an average a level over the five minutes, as well as a peak ammonia level achieved during the five minutes. After the ements were te, the d fecal matter was removed, and approximately 50 g of fresh fecal matter and 5 mL of urine were added. The containers were resealed. These steps were continued daily for 1 week to determine relative cies of the products. A one-time one-hour-interval a reading was taken on each of the containers.

After 8 days, the average ammonia level readings taken over 5-minute intervals every 24 hours showed that a production was much lower on the CLOE-treated litter than on the untreated control (see Figures 14A and 14B).

Example 7 Microbiology analysis Microbiological studies were done to demonstrate that the processes of odor formation are directly related to microbiological activity in the waste and waste environment. Inhibiting or controlling microbial activity should have a cial effect on the reduction of odors. CLOE has a direct effect on this microbial activity, rather than ameliorating the odors by absorbing them, as other cat litter treatment products do. To demonstrate this quality, approximately 0.5 g of CLOE were placed in the center well of a potato dextrose agar (PDA) plate, which had been covered with a lawn of bacteria derived from fresh solid cat waste. The plates were ted at 23°C for 1 week and photographed. The series of photographs shown in Figures 15A and 15B indicate that the ite control (15A) had massive amounts of bacterial colonies growing all over the plate, including in those areas close to the well containing the litter. In contrast, the CLOE treatment (4 ml S3 per pound (0.45 kg) of carrier, 15B) was virtually free of ial colonies around the well of the plate, but it did sport some growth of Penicillium sp., which is inherent to the carrier substance and does not contribute to odor production. Please also note the Penicillium sp. in the control well.

Clearly, the antimicrobial activity of the CLOE product is directly related to its effectiveness as a cat litter treatment and its ability to reduce ammonia and other odors emanating from animal (specifically cat) waste, as manifested by many users. This is also confirmed by the ability of the product to inhibit and kill waste-associated microbes such as E. coli. The CLOE formula is absorbed by the carrier substances, but it is also slowly released over time, and, as such, can effectively act at some distance from the point source of the bentonite or zeolite carrier particulate.

Example 8 Chicken Litter ent Comparative Efficacy g 1 ft.2 (0.09 m2) plastic snap-seal-top containers were filled with pine shavings and the desired bedding treatment, in the proportions indicated by the packaging instructions (Figure 16).

For these tests, Barnyard g at the rate of 15 ml per lb (0.45 kg) of e and an untreated zeolite control were tested, as these products are the more popular items on the market. A constant temperature was maintained in the testing ty for the on of the tests (e.g. 70°F ). About 50 g of chicken feces were added to treated containers and sprayed with about 2 mL of water. At 24 hour intervals, the ammonia level in each box was measured using the Z-800 ammonia meter. The measurements were done by placing the ammonia meter inside each box for respective 5-minute intervals, minimizing the amount of time the container spent open. The ammonia meter yielded an average a level over the five s, as well as a peak ammonia level achieved during the five minutes. About 50 g of fresh fecal matter and 2 mL of water were added each day after measurements were complete, and ner was resealed.

These steps were continued for 3 weeks to determine relative efficacy of the formula. A onetime one-hour-interval a reading was taken on each of the containers.

After 8 days, the average ammonia level readings taken over 5-minute intervals every 24 hours showed that ammonia production was highest on the zeolite control and lowest on the Barnyard Bedding-treated bedding (Figure 17A and 17B).

Example 9 Large Animal Stall Litter Amendment Comparative cy Testing 1 ft.2 (0.09 m2) c snap-seal-top container was filled with pine shavings (a commonly used bedding material for large animals) and the desired bedding treatment, in the proportions ted by the packaging instructions (Figure 18). For these tests, Barnyard Bedding, and an untreated zeolite control were tested. A constant temperature was maintained in the testing facility for the duration of the tests (e.g. 70°F (21°C)). About 100 g of fresh horse manure and about 10 mL of urine were added to treated ners. After 24 hours, the Z-800 ammonia meter was placed inside each box to make ements at respective 5-minute intervals, minimizing the amount of time the ner was open. The ammonia meter yielded an average ammonia level over the five minutes, as well as a peak ammonia level achieved during the five minutes. After measurements were complete, the day-old manure and urine-soaked pine bedding were removed. The recommended proportion of bedding treatment for wet spots plus about 100 g fresh manure and about 10 mL of urine were added, and each ner was resealed. These steps were continued for 1 week to determine relative efficacy of the products. A one-time onehour-interval ammonia reading was taken on each of the containers.

After 8 days, the e ammonia level readings taken over 5-minute intervals every 24 hours showed that ammonia production was highest on the control bedding and lowest on the Barnyard g-treated g (Figures 19A and 19B).

Example 10 ent of Calf Scours with Formula S-3 Calf Scours is a calf diarrheal disease caused primarily by viral and bacterial infection of the calf. In some instances, scours can occur in upwards of 70% of calves in a herd, and cause death to 50% of the infected calves. Although there is a viral etiology to these events, the most common cause is one of more pathogenic bacterial strains of Escherichia coli, followed by strains of Cryposporidia and Salmonella.

The minimum inhibitory concentration (MIC) of S-3 to E. coli is < 0.00125 %. Also see Table 5, above. Accordingly, a solution of about 1% S-3 at 50 ml may be effective to treat a calf ing with scours. A solution (S-X) was prepared for testing on calves diagnosed with the classical symptoms of scours. 2014/045297 The S-X formula contains the following ingredients: Per 100 ml: 1 g glucose 1 g whey protein 0.25 g KCl 0.25 g MgSO4 0.5 g NaCl 1 ml of 8-3 Glucose and whey protein were added to provide a nutritional supplement to the treated animals, whereas the other salts were added to e the electrolyte balance to the animal. The 8-3 ent is present to inhibit and kill pathogenic bacteria.

A first test was done on 5 newly born Holstein calves not having scours in order to learn if the S-X solution was toxic or was producing any side effects. Each y calf was administered 50 ml of the S-X solution and after 1 day, and into several weeks later, no adverse side effects were noted, and particularly, no signs of chemical side effects or abnormal behavior..

Arrangements were then made to do in vivo animal testing with the S-X mixture at a ranch in Bozeman, Montana. ng animals (Angus breed) were first reported during cold damp weather several weeks prior. Each scoured animal had all of the symptoms associated with this disease. Doses for each animal were set at 50 ml per animal per treatment. n calves authenticated as having scours were d with 50 ml of solution via the oral cavity by tubing. Thirteen calves, having been treated with 1 dose, recovered overnight.

Two animals required a second dose and recovered overnight after the second dose. Figure 20A shows one of the two scoured calves (tag 166) that had to receive a second 50 ml treatment of the S-X solution (image taken prior to administration of S-X solution). Note the large pile of excrement in the lower right hand comer and the head and ears down and drooped (Figure 20A).

One day after the second treatment with S-X solution, the calf was ambulatory and free of diarrhea (Figure 20B). The second day after the second S-X treatment, the calf was nursing its mother.

No deaths were reported in this experiment. The ranch owners reported that the S-X solution was far or to all other treatments they had used to-date. Accordingly, S-X solution represents a safe, fast and effective ent of scours.

Example 1 1 Livestock scours treatment A scours treatment formula was developed that contained the 8-3 formulation plus sugar, amino acids, sodium and potassium chloride and magnesium acetate. Many animals having infectious scours (caused by a pathogen) were treated. Typically, if the infectious scours is involved the stools are yellow to brownish to somewhat greenish. Also if a parasite is causing scours, the fecal matter ns blood and this is evident. If non-infectious scours (milk scours) is ed, the fecal matter is h. In this study at least two animals had milk scours and did not recover. Likewise, it appeared that one animal had parasitic scours and it too did not recover.

Basically, all other animals (having viral or bacterial caused scours) did recover when given S-X treatments. In about 90% of the cases recovery was within 12-24 hr with signs of recovery occurring within 3-4 hr. In a few cases, recovery took two days requiring a second treatment.

This is unlike any other treatment available. The material is delivered orally via stomach tube or syringe. Other treatments using antibiotics and nt electrolyte solutions do manage to assist the animal but ry is not certain as is mostly the case with the 8-3 treatment.

Exemplaryformulation and treatment 0fScours in calves Per 90 ml of water: 1 g of glucose 1 g glycine 0.5 g ofNaCl 0.25 g KCl 0.25 g Mg acetate 1 ml of 8-3 containing 0.7ml of propanoic acid and 0.2 ml of isoamyl hexanoates. 50 ml per animal was administered via syringe or h tube per treatment and some atment was necessary if the animal did not recover in 24 hr.

Exemplaryformulation and treatment 0fScours in piglets Per 90 ml of water: 1 g of glucose 1 g glycine 0.5 g of NaCl 0.25 g KCl 0.25 g Mg acetate 0.1 g KH2PO4 2 ml of S-3 containing 0.7 ml of propanoic acid and 0.2 ml of isoamyl hexanoates. 1-2 ml per piglet administered via a syringe.

S-X Scours Treatment Field Study Case 1 – Ranch 1 May 16, 2014 - One calf had come down with scours on the 6th of May and had been d with Banomine and given two shots of LA-200 9 (an anti-infectious drug). olyte solutions were also given on a daily basis in the dosage of 1 pint (473 mL); however, the animal did not recover and languished for 9 to 10 days with chronic scours. The S-X solution was sent on the morning of May 17th and the scouring calf was administered 50 ml orally by syringe. It was noted that the calf was dramatically improved in condition by the evening and completely better on the morning of May 18th. The calf showed no further signs of scours as of May 22, 2014. These s demonstrate that virtually all scours treatments on this animal had failed and that it was not in a ry stage until the S-3 treatment was given.

Case 2 – Ranch 2 Ranch 2 experienced an influx of scouring calves and ity in the late winter of 2014.

The S-X technology solution was provided to them, and the ranchers used the solution for treatment of calves via stomach tubing. Three calves were treated in this manner. Recovery from scours for these calves ed within 24 hours after treatment, and there were no other known medications administered at the same time as the S-X treatments that could have contributed to recovery. Sick animals were taken into the barn and photographed during their recovery. One of these animals is pictured in Figure 21.

WO 03082 Case 3 — Ranch 3 Ranch 3 experienced a particularly cold winter during the calving season, including high winds and a large amount of snow fall. These conditions make scouring a more common occurrence for calves.

S-X treatments for scouring calves were administered at this ranch from April 2 to April 24, 2014. Eleven animals were treated with 50 ml dosages using the stomach tubing method.

Results were successful, with one dose in nine head; while one animal had to be treated a second time and another one needed three separate treatments. In some cases, S-X was not the only treatment given. Some of the animals also presented with symptoms of pneumonia and needed does of Baytril, sulpha pills, or Nuflor. All animals that were treated with the S-X solution recovered while most (9) recovered within twenty-four hours after treatment.

Case 4 — Dairy 1 May 15, 2014 — Dairy 1 is a holstein dairy cow operation. This dairy houses 300 animals whose health and everyday needs must be met. Dairy has been shown to have the rotaVirus as a source for scours, which was noted by the veterinary center located near their dairy. The S-X treatment was administered to 7 young animals that had scours by oral syringe ation. All of the animals that were given the S-X treatment recovered. All of the animals except one recovered within 24 hours, and one after the second treatment of S-X.

According to Dairy 1, in December of 2013, 30 of their calves were lost to scours, even though these calves had been given multiple electrolyte treatments as well as antibiotics.

Treatment of these calves usually took 5-7 days with le treatments, as compared to the 1 day of 1-2 dosages of S-X ents. Administration of the ent Via oral drench was preferred by Dairy 1 and proved to be effective.

The or of Dairy 1 remarked, “Need more, since the stuff really works.” She was ing to the S-X solution and their s with these treatments. The dairy will continue treating calf scours with the S-X technology as well as providing information on animals that are subsequently tested with the S-X formula.

Case 5 — Ranch 4 The S-X technology was also tested at a Hutterite swine production facility the week of April 14th, 2014 where ds of piglets were exhibiting scours. The presence of the PED virus in this pig population was confirmed by Newport Labs, Worthington, MN. According to the producer, over 850 s had died in the previous three weeks, which represents nearly a 100 t fatality in infected piglets.

The producer was interviewed about the results of his trial with the piglet formula of the S-X technology for use on scouring pigs on April 19, 2014. The producer noted that on or around the 12th of April, 2014 an 8-day old piglet with scours was administered 6 ml of the S-X formula orally via syringe. After 5 hours the piglet was better and the next day there was no evidence of scours. Furthermore, on the lSth of April, 10 piglets that were all 14 days old showed evidence of scouring with the classic symptom of dark yellow loose stools. These piglets were administered 4 ml of S-X solution orally through a syringe, and within 24 hours each animal was completely “dry.” The er also ted that from his previous experiences with the disease, he would have expected many ties. onally, on or around April 19th 10 piglets that were 3 days old showed signs of scours and were given 2 ml of the S-X solution via syringe. All of these s also remained alive after several weeks. Another treatment was administered for 30 piglets that were 3 days old showing signs of scouring. These 30 piglets were given 3 ml of the S-X solution and all piglets remained alive. If the treatment had not been administered, the producer would have expected mortality for nearly all of these animals, based on his previous experiences. The producer also administered Tylan 40-50 to each of the 3 day old piglets in the study whose treatments were on April 15th and 19th. Tylan is an antibiotic that is used to treat pneumonia.

The producer felt that the Tylan-40 paired with the S-X treatment was responsible for the survival of these young animals; however, according to professionals in the field, antibiotics are generally not ive against inal viral and bacterial infections. Although not wishing to be bound by any particular theory, in this case, Tylan-40 likely had no effect on the survival of the piglets.

Since using the S-X solution to treat his piglets, the producer has not lost any animals to scours. Additionally, as of May 27, 2014, samples from the piglets that had been sent to Norwalk labs after the addition of S-X treatments confirmed that PED was no longer present. This finding indicates that the S-X on is successful at treating scours in pigs at the Harlowton colony.

Furthermore, the disappearance of the PED virus from the area may be uted to the S-X ents since all piglets with scours were treated with the technology and recovered.

Case 6 — Ranch 5 Ranch 5 near the Canadian border participated in S-X treatments for scours for their beef cattle ranch. The temperatures during calving season were particularly low during the past winter with driving winds and high snow falls. The S-X solution was provided early in April and the first date of treatment that followed was on April 6, 2014. -one animals were treated only with the S-X solution for conditions of scouring and s were treated by stomach tube stration of 50 ml of S-X solution. After 24 hours, 18 of the calves that had been treated with the S-X solution recovered from scouring; however, 3 animals needed a dosage re- administration. These animals soon recovered after the treatment. Of the 21 animals treated, 8 sed symptoms of pneumonia and were given Nuflor. Recovery of animals d with S- X was not related to the treatment for the incidence of pneumonia. The last date of treatment was on April 18, 2014. In all, approximately 85 percent of the animals treated with the S-X technology recovered with one dose of the solution. These results demonstrate that S-X technology required less time and was more effective than traditional forms of treatment for scouring s.

Case 7 — Ranch 6 Ranch 6 is a dairy operation that used the S-X technology as a scours treatment in mid- April of 2014. The dairy has about 100 head of Holstein milk cattle with various other animals, including beef cattle. The incidence of scours on the ranch is particularly high and most animals acquire scours soon after birth. The S-X formula was given to the dairy and it was administered to both beef calves and in calves in 50 ml doses through oral syringes.

Initial treatments of the S-X formula were given to 8 calves in 50 ml doses via syringe, 7 of which had displayed the typical creamy yellow scouring, and l calf (number 80) with white pasty scouring that developed into watery scours after two days. This calf’ s condition was l of milk scours. This ular calf was treated with S-X well after its symptoms had developed, and it died 4 days later. It was suspected that this particular calf’ s scours was nutritionally caused because of the characteristics of the diarrhea, in which case the S-X technology would not have been effective. Most of the animals that were treated with the S-X solution recovered and were completely better within 24 hours; however, one holstein calf took 48 hours to fully recover. Additionally, one beef calf (number 34 as an untreated control) at the ranch was noted to have scours and was not given a dose of the S-X solution along with the other animals and it died within two weeks. Figure 23 is a series of images showing a calf treated with S-X before and after treatment.

Case 8 – Ranch 7 The owners of Ranch 7 were interested in using S-X logy in the early spring of 2014 for treating newborn calves that developed . The S-X solution was given to the owners and over the course of several weeks, calves that showed signs of scouring were immediately treated in the pasture with 50 ml of the S-X solution in two doses of 25 ml in an oral syringe. At least 15 calves were treated with the S-X solution and every one of them except for one recovered in 24 hr. The one calf that did not recover in 24 hours had white feces that could have been attributed to “milk scours.” This calf also had pneumonia so it was also treated with Nuflor and a drench. It was also administered two additional treatments of the S-X solution. The calf did recover from scours and is now in normal condition. The owner noted that most of the time calves recovered within 3 to 4 hours after treatments of the S-X solution. The owner also commented that improvement was recognized with the calves’ stoppage of “teeth grinding,” and in their general se in alertness. The owner noted that the oral syringe method of S-X on treatment was very easy for her to administer dosages to the 100 lb (45.36 kg) .

These results demonstrate that administration of S-X can be performed using either the stomach tube or the syringe method.

Case 9 – Ranch 8 Experiments on beef calves with scours took place at Ranch 8 in at an elevation of 4,459 feet (1,359 m), from May 4, 2013 to May 21, 2014, concentrated in the spring of 2013 and the winter and spring of 2014. On this ranch, 300 calves are born in the spring and 300 are born in the fall. One hundred and forty two distinct calves were d with an S-X on or a combination of S-X solution and other medications. The initial S-X formula was used through January 2014, after which an improved formula of the S-X logy scours treatment was used.

Temperatures varied from –20°F ) to up to 50°F (10°C) in the months of February and March. Significant snow and winds were observed during this time period with dramatic temperature swings reported.

A large number of calves exhibited clinical signs of scours (droopy ears, sullen eyes, and profuse ea). These calves were given 50 mL of the S-X on through a stomach tube system and checked approximately six hours later to determine if they were recovering or if readministration of the drug was needed. Of the 243 calves treated, 36 were either given only the solution for the first or second dose or the solution plus a vitamin supplement, while the rest were administered standard antibiotics along with the S-X scours treatment. Twelve of the S-X- only treatments were administered as a second or third dose within the same day. In all, 243 treatments included the S-X solution and 29 of those were treated either 2 or 3 times. Total individual calf s that were treated with both formulae ed 142. Drugs that were typically given along with the S-X treatment included: Excede (treats respiratory infection), probiotics, Toxiban (absorbs toxins with charcoal), Noromycin LA (antibiotic for use on pinkeye, foot rot, and other infections), multivitamins, Inforce 3 (a three-way respiratory vaccine), Draxxin (antibiotic for pinkeye, foot rot, or respiratory disease), and sulpha tablets (sulfonamides for anti-bacterial treatments).

The owners of Ranch 8 were interviewed on March 3, 2014 on their experiences with the S-X treatment for scours. Scours was first reported for the calving season on February 27, 2014, and 40 doses were supplied at 50 mL each. From February 27 until March 3, 15 calves with signs of scouring had been treated with S-X technology. Thirteen of those 15 recovered overnight after one dose, while 2 required a second dose and recovered overnight with no ity in either instance. Half of the calves were treated in the pasture with only 6 brought in to the barn. Normal treatment for scours includes electrolytes, IV administration of fluids, and some antibiotics such as tetracycline.

The ers observed that some of the calves treated had pneumonia and other tions were administered; however, it was also noted that the S-X ents were far superior to other tions and credited its use with a quick and full recovery. It was estimated that without the S-X, one-third or more of the calves with scours would have died.

Additional observations of the S-X ent were that it was easy to use and carry when working the herd, that it was a quick treatment option and that antibiotic treatment was not required if the scours was caught quickly enough. Figure 24 is a series of images showing a calf d With S-X before and after treatment.

Table 7 depicts the S-X treatments administered at Ranches 3, 5, and 8 Without any additional medications given besides Vitamin ments.

Table 7: S-X Treatments Without other medications Ranch S—X Date Calf Treatment number 000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO S-l 13 Y122 1st S-l 5/4/2013 Y306B 1st S-l 5/6/2013 Y350a 1st S-3 2/24/2014 Y3742 1st S-3* 2/27/2014 Y26262 1st S-3* 2/27/2014 Y321 1st S-3* 2/27/2014 Y383 1st S-3 3/2/2014 R18361 1st S-3 3/2/2014 Y3730 1st S-3 3/2/2014 Y387 1st S-3 3/3/2014 G032 1st S-3 3/3/2014 Y166461 1st S-3 3/3/2014 Y402 1st S-3 3/4/2014 G03 2nd S-3 14 G3731 1st S-3 3/4/2014 R1396 1st S-3 3/4/2014 Y29092 1st S-3 3/5/2014 G309 1st S-3 3/5/2014 Y29902 1st S-3 3/5/2014 Y3311 1st S-3 3/5/2014 Y8A20 1st S-3 3/6/2014 R2451 2nd S-3 3/6/2014 Y163391 1st S-3 3/9/2014 Y2014 2nd S-3 3/12/2014 R215 1st S-3 014 Y16629 3rd S-3 3/15/2014 Y2014 2nd S-3 3/16/2014 R26861 2nd S-3 3/16/2014 Y2062 2nd S-3 3/16/2014 Y3619 1st S-3 3/17/2014 Y20060 2nd S-3 3/18/2014 Y3630 2nd S-3 3/18/2014 Y80842 2nd 8 S-3 014 R616 2nd 8 S-3 3/27/2014 Y411 2nd 8 S-3 014 R616 1st S3 4/6/2014 516 1st S3 4/6/2014 1122 1st S3 4/6/2014 1255 1st S3 4/6/2014 8104 1st S3 4/6/2014 9203 1st S3 4/7/2014 7490 1st S3 4/8/2014 173 1st S3 4/8/2014 1241 1st S3 4/8/2014 5416 1st S3 4/12/2014 1203 2nd S3 4/12/2014 2487 1st S3 4/12/2014 2637 1st S3 4/16/2014 1219 2nd S3 4/18/2014 711 1st S3 4/18/2014 1000 1st S3 4/18/2014 1636 1st S3 4/18/2014 k23 1st 3 S-X 4/18/2014 2431 1st * Received multivitamin supplement Table 8 depicts all S-X treatments given regardless of Whether any additional medications were administered for Ranches 3, 5, and 8.

Table 8: All S-X treatments Treatment Ranch S—X Date Calf Additional Medication number 8 S-1 5/4/2013 Y122 1st 8 S-1 5/4/2013 Y306B 1st 8 S-1 13 Y350a 1st 8 S-1 5/ 15/2013 Y163 1st \oromycin LA, Toxi Ban, Nas 8 S-1 5/15/2013 Y169 1st \oromycin LA 8 S-1 5/15/2013 Y3351 1st \oromycin LA 8 S-1 5/18/2013 R22326 1st \oromycin LA 8 S-1 5/18/2013 Y169 1st \oromycin LA 8 S-1 5/18/2013 Y3351 1st cin LA 8 S-1 5/29/2013 Y2886 1st \oromycin LA, Toxi Ban 8 S-1 10/21/2013 Y311 1st Excede 5cc 8 S-1 2013 R287 1st \oromycin LA 5cc 8 S-1 10/25/2013 R325 1st \oromycin LA 5cc 2014/045297 00000000000000000000000000000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO S-l 10/25/2013 Y238 1 st \oromycin LA 5cc 2/23/2014 G309 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y124981 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y14146 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y17739 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y36192 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y3742 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y405 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/23/2014 Y420 1 st \oromycin LA 5cc, Toxi Ban, sulpha 2/24/2014 Y3742 1 st 2/27/2014 Y26262 1 st Multivitamin 2/27/2014 Y321 1 st Multivitamin 2/27/2014 Y336 1 st \Ioromycin LA, multivitamin 2/27/2014 Y383 1 st multivitamin 2/27/2014 Y422 1 st 14 R18361 1 st 3/2/2014 Y3730 1 st 3/2/2014 Y387 1 st 3/3/2014 G032 1 st 3/3/2014 Y166461 2nd 3/3/2014 Y1 883 52 1 st Noromycin LA, Toxi Ban, itamin 3/3/2014 Y402 1 st 3/4/2014 G03 1 st Noromycin LA, Toxi Ban, multivitamin 3/4/2014 G03 2nd 3/4/2014 G3731 1 st 3/4/2014 R1396 1 st 3/4/2014 Y29092 1 st 3/4/2014 Y389 1 st Noromycin LA, Toxi Ban 3/5/2014 G309 1 st 3/5/2014 Y29902 1 st 3/5/2014 Y3311 1 st 3/5/2014 Y3779 1 st Toxi Ban 3/5/2014 Y8A20 1 st 3/6/2014 G0561 1 st Toxi Ban 3/6/2014 G3731 1 st Noromycin LA, Toxi Ban 14 R1396 1 st Noromycin LA, Toxi Ban 3/6/2014 R2451 1 st Noromycin LA, Toxi Ban 3/6/2014 R2451 2nd 14 R2456 1 st Toxi Ban 3/6/2014 Y163391 1 st 3/6/2014 Y20251 1 st Toxi Ban 14 Y3859 1 st cin LA, Toxi Ban 3/6/2014 Y408 1 st Toxi Ban 00000000000000000000000000000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO 3/7/2014 G03 1 st \oromycin LA 5cc 3/7/2014 G522 1 st \oromycin LA 5cc 14 R22519 1 st \oromycin LA 5cc 3/7/2014 Y16131 1 st \oromycin LA 5cc 3/7/2014 Y1951 1 st \oromycin LA 5cc 3/7/2014 Y29961 1 st \oromycin LA 5cc 3/7/2014 Y29962 1 st \oromycin LA 5cc 3/7/2014 Y3779 1 st \oromycin LA 5cc 14 R2451 1 st \oromycin LA 5cc 3/8/2014 Y28869 1 st \oromycin LA 5cc 3/8/2014 Y29962 1 st Excede 3cc 3/9/2014 G235 1 st \oromycin LA 5cc 3/9/2014 R13951 1 st \oromycin LA 5cc 3/9/2014 Y163391 1 st \oromycin LA 5cc 3/9/2014 Y1954 1 st Excede 3cc 3/9/2014 Y2014 2nd 3/9/2014 Y2014 1 st \oromycin LA 5cc 3/9/2014 Y2220 1 st cin LA 5cc 3/9/2014 Y3016 1 st \oromycin LA 5cc 3/9/2014 Y3042 1 st \oromycin LA 5cc 3/9/2014 Y3562 1 st \oromycin LA 5cc 3/10/2014 Y166461 1 st Toxi Ban 014 Y19541 1 st \oromycin LA 5cc 3/10/2014 Y2366 1 st \oromycin LA 5cc 3/10/2014 Y28392 1 st Toxi Ban 3/10/2014 Y2985 1 st \oromycin LA 3/10/2014 Y3630 1 st \oromycin LA 3/10/2014 Y365 1 st \oromycin LA 3/10/2014 Y401 1 st \oromycin LA 5cc 3/11/2014 R2391 1 st \oromycin LA 3/11/2014 Y2014 1 st cin LA 5cc 014 Y2162 1 st Excede 3cc 3/11/2014 Y2985 1 st \oromycin LA 5cc 3/11/2014 Y2985 1 st \oromycin LA 5cc 3/11/2014 Y3042 1 st Excede 3cc 3/12/2014 R215 1 st 3/12/2014 Y19349 1 st Noromycin LA 5cc 3/12/2014 Y2116 1 st Excede 3/12/2014 Y2366 1 st Excede 5cc 3/12/2014 Y2985 1 st Excede 3/12/2014 Y29962 1 st Noromycin LA 5cc 014 Y3630 1 st Excede 5cc 3/12/2014 Y64659 1 st Noromycin LA 5cc 00000000000000000000000000000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO 3/13/2014 G3731 1 st \oromycin LA 5cc 3/13/2014 R215 1 st Excede 5cc, Toxi Ban 3/13/2014 Y16629 1 st \oromycin LA 5cc 3/13/2014 Y19349 1 st \oromycin LA 5cc 3/13/2014 Y28392 1 st Excede 3/14/2014 Y1106 1 st \oromycin LA 5cc 3/14/2014 Y16629 1 st Excede 3cc 014 Y2951 1 st \oromycin LA 5cc 3/15/2014 R26861 1 st \oromycin LA 3/15/2014 R2902 1 st \oromycin LA 5cc 3/15/2014 Y16629 3rd 3/15/2014 Y2014 1 st \oromycin LA 3/15/2014 Y2014 2nd 3/15/2014 Y2366 1 st EX 3/15/2014 Y28392 1 st Noromycin LA 5cc 3/15/2014 Y2985 1 st Draxxen 3/15/2014 Y356 1 st Noromycin LA 3/15/2014 Y3619 1 st Noromycin LA 3/16/2014 R21441 1 st Noromycin LA 5cc, Toxi Ban 3/16/2014 R26861 2nd 014 Y2062 2nd 3/16/2014 Y2062 1 st \oromycin LA 5cc 014 Y2382 1 st \oromycin LA 5cc 3/16/2014 Y264 1 st \oromycin LA 5cc 3/16/2014 Y3619 1 st 3/17/2014 G235 1 st \oromycin LA 5cc 3/17/2014 G3731 1 st \oromycin LA 5cc 3/17/2014 R13951 1 st \oromycin LA 5cc 014 R317 1 st \oromycin LA 5cc 014 Y20060 2nd 3/17/2014 Y20060 1 st cin LA 5cc 3/17/2014 Y21 16 1 st \oromycin LA 5cc 3/17/2014 Y2382 2nd \oromycin LA 5cc 3/17/2014 Y264 1 st \oromycin LA 5cc 3/17/2014 Y2951 1 st \oromycin LA 5cc 3/17/2014 Y3630 1 st \oromycin LA 5cc 3/17/2014 Y80842 1 st \oromycin LA 5cc 014 G34491 1 st \oromycin LA 5cc 3/18/2014 G4335 1 st \oromycin LA 5cc 3/18/2014 Y3630 2nd 3/18/2014 Y64659 1 st \oromycin LA 5cc 3/18/2014 Y80842 2nd 3/19/2014 R215 1 st \oromycin LA 5cc OOOOOOOOOOOOOOOOOOOO00000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO 3/19/2014 R29092 1 st ycin LA 5cc 3/19/2014 Y2382 3rd \orornycin LA 5cc 3/19/2014 Y2951 1 st \orornycin LA 5cc 014 Y2985 1 st \orornycin LA 5cc 3/19/2014 Y3619 1 st \orornycin LA 5cc 014 Y64659 2nd \orornycin LA 5cc 3/19/2014 Y80842 3rd Excede 3cc 3/20/2014 Y2951 1 st \orornycin LA 5cc 3/20/2014 Y411 1 st \orornycin LA 5cc 3/20/2014 Y80B42 1 st Excede 3cc 014 R616 1 st ycin LA 5cc 3/22/2014 Y411 3rd Excede 3cc 3/23/2014 R20016 1 st \orornycin LA 5cc 014 R616 2nd \orornycin LA 5cc 3/23/2014 Y2382 1 st ycin LA 5cc 3/23/2014 Y2951 1 st \orornycin LA 5cc 3/24/2014 R1836 1 st \orornycin LA 5cc 3/24/2014 R29092 1 st \orornycin LA 5cc 3/24/2014 R616 3rd ycin LA 5cc 3/24/2014 Y10651 1 st Draxxen, Inforce 3 3/24/2014 Y321 1 st Draxxen, Inforce 3 9”DJ 3/24/2014 Y3619 1 st Norornycin LA 5cc 3/24/2014 Y411 1 st Norornycin LA 5cc 3/25/2014 R1836 2nd Norornycin LA 5cc 3/25/2014 R290 1 st Draxxen, sulpha 3/25/2014 R29092 1 st Norornycin LA 5cc 3/25/2014 Y29852 1 st Norornycin LA 5cc 3/25/2014 Y3619 2nd Norornycin LA 5cc S-3* 3/25/2014 Y368 1 st Draxxen, sulpha S-3* 3/25/2014 Y3742 1 st Draxxen, sulpha S-3* 3/25/2014 Y3862 1 st Draxxen, sulpha S-3* 3/26/2014 G1310 1 st Draxxen, sulpha S-3* 3/26/2014 R239 1 st Draxxen, sulpha S-3* 3/26/2014 R239 2nd Draxxen, sulpha S-3* 3/26/2014 R3000 1 st Draxxen, sulpha S-3* 3/26/2014 R3041 1 st Draxxen, sulpha S-3* 3/26/2014 Y1606 1 st Draxxen, sulpha S-3* 3/26/2014 Y20142 1 st Draxxen, sulpha S-3 3/26/2014 Y259 1 st Norornycin LA 5cc S-3* 3/26/2014 Y28869 1 st Draxxen, sulpha S-3* 3/26/2014 Y29062 1 st Draxxen, sulpha S-3* 3/26/2014 Y30162 2nd Draxxen, sulpha S-3* 3/26/2014 Y30162 1 st Draxxen, sulpha 2014/045297 00000000000000000000000000000000000000000000OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO S-3* 3/26/2014 Y331 1 st n, sulpha 3/26/2014 Y3619 3rd Noromycin LA 5cc 3/27/2014 R1836 1 st Noromycin LA 5cc 3/27/2014 R616 1 st Noromycin LA 5cc 014 R616 2nd 3/27/2014 R8461 1 st Draxxen, sulpha 3/27/2014 Y411 1 st Noromycin LA 5cc 3/27/2014 Y411 1 st S-3* 3/28/2014 Y1361 1 st Draxxen, sulpha S-3* 3/28/2014 Y1606 1 st Draxxen, sulpha S-3 3/28/2014 Y266962 1 st Noromycin LA 5cc S-3* 3/29/2014 G1310 1 st Draxxen, sulpha S-3* 3/29/2014 R2028 1 st Draxxen, sulpha S-3* 3/29/2014 Y16932 1 st n, sulpha S-3* 3/29/2014 Y18835 1 st Draxxen, sulpha S-3* 3/29/2014 Y3590 1 st Draxxen, sulpha S-3* 3/30/2014 G3060 1 st Draxxen, sulpha S-3 3/30/2014 R616 1 st S-3* 3/30/2014 Y166461 1 st Draxxen, sulpha S-3* 3/30/2014 Y2116 1 st Draxxen, sulpha S-3 3/30/2014 Y259 1 st Noromycin LA 5cc S-3* 3/31/2014 G131 1 st Draxxen, sulpha S-3* 3/31/2014 G5052 1 st Draxxen, sulpha 3/31/2014 G57 1 st Noromycin LA 5cc 3/31/2014 R3691 1 st Noromycin LA 5cc 3/31/2014 Y1124 1 st Noromycin LA 5cc S-3* 3/31/2014 Y119 1 st Draxxen, sulpha 014 Y26682 1 st cin LA 5cc S-3* 3/31/2014 Y2839 1 st Draxxen, sulpha S-3* 3/31/2014 Y36192 1 st Draxxen, sulpha S-3* 3/31/2014 Y365 1 st Draxxen, sulpha S-3* 3/31/2014 Y384 1 st Draxxen, sulpha S-3 3/31/2014 Y386 1 st Noromycin LA 5cc S-3 3/31/2014 Y424 1 st Noromycin LA 5cc S-3* 4/1/2014 B1395 1 st Draxxen, sulpha S-3* 4/1/2014 G5052 2nd Draxxen, sulpha S-3 4/1/2014 Y1126 2nd Noromycin LA 5cc 4/1/2014 Y2446 1 st Noromycin LA 5cc S-3 4/1/2014 Y266962 2nd Noromycin LA 5cc S-3 14 Y29852 1 st Noromycin LA 5cc S-3* 4/1/2014 Y3279 1 st n, sulpha S-3* 4/1/2014 Y3412 1 st Draxxen, sulpha S-3* 4/1/2014 Y43 1 st Draxxen, sulpha 030303030301mm010101010101mm010101010101mmmmmmoooooooooooooooooooooooooooooo S-3* 4/1/2014 Y592 1 st Draxxen, sulpha S-3* 4/2/2014 Y17739 1 st Draxxen S-3* 4/2/2014 ‘Y26262 1 st Draxxen, sulpha S-3 14 Y29852 2nd Noromycin LA 5cc S-3* 4/2/2014 Y399 1 st Draxxen, sulpha S-3* 4/3/2014 Y121242 1 st Draxxen S-3* 4/3/2014 Y16936 1 st Draxxen S-3* 4/3/2014 Y411 1 st Draxxen /21/2014 G34491 1 st Noromycin LA 5cc 014 R1836 1 st Noromycin LA 5cc /21/2014 R20016 1 st Noromycin LA 5cc /21/2014 R2616 1 st cin LA 5cc /21/2014 R29092 1 st Excede 3cc /21/2014 Y411 2nd Noromycin LA 5cc /21/2014 Y5861 1 st Noromycin LA 5cc 14 8104 1 st 4/6/2014 9203 1 st 4/6/2014 1122 1 st 4/6/2014 516 1 st 4/6/2014 1255 1 st 14 1255 2nd Nuflor 4/7/2014 7490 1 st 14 1203 1 st Nuflor 4/8/2014 1241 1 st 4/8/2014 5416 1 st 4/8/2014 173 1 st 4/12/2014 2363 1 st Nuflor 4/12/2014 9203 1 st Nuflor 4/12/2014 1203 2nd 4/12/2014 2637 1 st 4/12/2014 2487 1 st 4/12/2014 2763 1 st Nuflor 4/14/2014 1219 1 st Nuflor 4/16/2014 1219 2nd 4/18/2014 1000 1 st 4/18/2014 1636 1 st 4/18/2014 k23 1 st 4/18/2014 711 1 st 4/8/2014 2012 1 st Drench 4/18/2014 Y273 1 st Drench, Baytril 4/18/2014 2431 1 st 4/18/2014 Y177 1 st Baytril 4/22/2014 Y82 1 st Drench, Baytril 3 S-X 4/23/2014 Y273 1st Suprio 3 S-X 4/24/2014 281 1 1st Drench, Nuflor 3 S-X 4/24/20 1 4 wI 1st Drench, Nuflor, sulpha 3 S-X 4/24/2014 1100 1st Baytril 3 S-X 4/25/2014 841 1st Drench 3 S-X 4/25/2014 longhorn 1st Drench 3 S-X 4/25/2014 452 1st Drench, Nuflor *indicates S-X ent through nasal passages (2cc) Example 12 Animal mastitis treatment The problem of mastitis in the mammary glands in animals is typically caused by infections brought about by E. coli or Staphyloccous aureus and other bacterial pathogens. The teat s inflamed and eventually the condition can spread to all other sectors of the mammary gland. Milk production ceases. If untreated, the animal can die. Most antibiotic ents are expensive and ineffective. In the past three months, a yew lamb and two dairy cows suffering with mastitis were treated with 15 mL per teat of the mastitis treatment solution.

Figure 25A depicts a teat of a sheep suffering from mastitis. The d animal was well developed in terms of the disease and it did not die but remains y. The y gland has ceased functioning. The S-3 formula was administered via syringe (Figure 25B). Two cows suffering with mastitis were in the earlier stages of this disease. Each was treated with 15 ml per infected teat and total ry was noted within 24 hr.

Exemplaryformulation ana1 treatmentfor mastitis offarm animals Per 90 ml of water: mg of cremophor or other appropriate surfactant 0.7 ml of oic acid and 0.2 ml of isoamyl ates The formulation was shaken well and administered to a cow up to 15 ml per teat with a syringe. The cremophor acts to bring the ingredients of the S-3 formulation into solution.

Example 13 MIC testing 0fS—3 ana1 S—4formulations MIC Protocol for testing S—3 and 8-4 Turbid bacterial cultures grown in the appropriate nutrient broth medium were adjusted to OD650 = 0.4 and subsequently d 1:100 in broth, representing a concentration of 1><106 CFU/ml. 50 ul of this e were added to each well except the negative control, in which 50 ul broth was added. The final amount of bacteria in each well was 5><106 CPU. ul stock B-23 antibiotic solution was added to 480 ul broth. 250 ul of this solution was diluted 1:2. This was repeated twice to form four progressively diluted otic solutions.

Dilutions are such that final concentrations of the antibiotic in the appropriate wells were equal to 1%, 0.5%, 0.25%, and 0.125% ofthe stock B-23 antibiotic solution.

A 96-well microtiter plate was used. 6 total treatments were : 1%, 0.5%, 0.25%, 0.125%, 0.061%, 0.03% and 0% otic with bacterial inoculum; and no bacterial inoculum.

Each ent was plated in triplicate.

Broth was added to each well to reach a final volume of 200 ul. In wells without bacterial inoculum or antibiotic solution, an additional 50 ul broth was added.

MIC plates were incubated at appropriate growth conditions to the time points recorded on result tables. End points were chosen when the positive control well was turbid.

The MIC point was taken as the lowest concentration at which no growth was evident.

Results The MICs were as follows for the following organisms: Bacillus subtilis: 0.06125% Vibrio cholerae: 0.06125% Pseudomonas aeruginosa: 0.125% Salmonella enterica serovar Typhimurium: 0.06125% Escherichia coli: 0.125% Methicillin—resistant Staphylococcus aureus: 0.06125% For other MIC tests o dextrose broth was used instead of nutrient broth and the tests were done in the same manner. The results were: Erwinia ora: 0.0612% Lactobacillus sp.: 0.0625% WO 03082 Erwinz'a car0t0v0ra: 0.125% The s demonstrate that the 8-3 and 8-4 are useful for the treatment of diseases in plants, animals and humans caused by microorganisms. These diseases include plant diseases caused by Erwinz'a and the problem in grain fermentation to produce l caused by Lactobacz'llus spp. biofllms produced by Pseudomonas. Additional diseases e food ailments caused by Salmonella, E. coli and general major diseases caused by MRSA.

Example 14 Raspberry treatments The results bed herein demonstrate that the S-X technology is useful for the preservation of fruit and vegetables during shipment and storage. The 8-3 formula was mixed to form two formulations: 1 ml of 8-3 per 10 g of ite (the 1:10 mixture); 1 ml of 8-3 to 20 g bentonite (the 1:20 mixture) or other carrier. 1 gram of the mixture was placed in a small plastic cup in the presence of store purchased rries. The materials were placed in a small clear c box, which was sealed and held at room temperature for 1 week, followed by examination for the ce of contaminating fungi. The results demonstrate that the normal flora of the fruit quickly brings about its decay after 1 week at room temperature (Figure 26A). However, use of the 1:10 mixture resulted in no decay (Figure 26B). However, the 1:20 mixture did not perform quite as well as the 1:10 mixture, as at least 1 berry showed decay. Nonetheless, the 1:20 mixture was useful for preventing decay in the berries, and the treated berries were edible. A similar experiment was conducted with store purchased Thompson delicious grapes and the results were similar, wherein the control grapes were observed to show decay, while the treated grapes were not decayed. The grapes were also , as 4 people ate them and provided an evaluation of their acceptability.

Example 15 Treatment 0ff00a’poisoning and/0r stomachflu in humans using S—X.

The symptoms and conditions of food poisoning and/or stomach flu in humans re similar to those occurring in animals suffering with scours. For example, possible symptoms include: abdominal cramps, diarrhea (may be ), fever and chills, headache, nausea, vomiting, and weakness (may be serious). Most people simply suffer through the experience (12-48 hr) by 2014/045297 doing their best to rest, and drink replacement fluids and minerals being lost through diarrhea and vomiting. It appears that no product is ble that provides instant relief.

However, in ten volunteers suffering with one or more of these ms, at least 10-15 ml of a l % S-3 formula was taken orally at the onset of symptoms or within a few hours of the appearance of symptoms. In all cases, the patients described feeling better within one to two hours after treatment. Fever, stomach pain, diarrhea and vomiting all ceased, and the patients fully recovered. All patients were adults, white and represented both male and female classes.

One patient, however reported that there was no difference noted in the stomach condition after taking a 10 ml dose of a l % S-3 formula. Although not g to be bound by any particular theory, it is suspected that the patient was experiencing a viral induced stomach infection that would not have responded to S-X treatment. heless, the fact that 90% of the people treated having such an immediate and complete recovery, combined with all of the animal studies on scouring, supports the hypothesis that the 8-3 is useful for treating humans suffering from stomach flu and h poisoning caused by bacteria. This hypothesis is further supported by the impressive MIC values of 8-3 against E coli and S. aureus, which are two known causal agents of food poisoning in people le 13).

Example 16 z's in dairy cattle and the S—X technology Treatment: A formula containing 2 % of the 8-3 ation in the presence of 5 mg of cremophor (a non- ionic solubilizer) in pure water is thoroughly mixed and is used as the treatment agent.

Eight dairy cattle suffering with preclinical to sub-clinical mastitis were treated with 12 ml of the formula per teat. In seven cases the treatment was repeated during the course of one day. In all cases the animals were fully recovered the following day. Although not g to be bound by any particular theory, the recovery of the animals is likely due to the fact that the common bacterial causes of mastitis, such as E. coli and S. aureus, are organisms that are ely sensitive to the S-X formulations described herein (see Example 13.) Example 17 S—3 Detergent Testing 2014/045297 Several detergents that were obtained through sample orders were tested with the 8-3 solution for effectiveness on surfaces that are notoriously ridden with a y of pathogens.

These surfaces included a laboratory floor, and the women’s bathroom floor, toilet bowl, and door handle. For the floor testing, about 5 ml of each of the ent solutions (with 1 ml of 8-3 per 100 ml of deionized water) was poured on different sections of the floor and wiped dry with a paper towel. When this section of the floor was dried then it was wiped with a Kimwipe and this was then wiped across the surface of a potato se broth petri plate. For the toilet bowl testing, a paper towel was wet with the detergent solutions and a section of the surface was wiped. Kimwipes were used again once the surface dried and further streaked across a potato dextrose broth plate. The procedure for the door handle was the same as that for the sink except only one of the detergents was tested along with a control. The s are depicted in Tables 9 and 10 below.

Table 9: Laboratory floor results ment l EXoeriment 2 Amount of deterent Chemoxide CAW 2 milliliter BioSoft D40 0.5 milliliter Lathanol LAL 1 gram BioTere AS-40 l milliliter Potassium cocoate 2 milliliter l 1 Table 9 shows the number of ial or fungal colonies that grew on potato dextrose broth plates that were streaked from samples wiped with the various detergents or with just the Kimwipe as a control after 48 hours. One milliliter of 8-3 was used per 100 milliliters of deionized water.

Table 10: Detergent Testing in s Bathroom Amount of Floor Colonies Toilet Bowl Door Handle detergent es Colonies Control 12 6 2 Sucra-el CF 1 milliliter —__ Chemoxide CAW 2 milliliter __— BioSoft D40 0-5 milliliter __— Lathanol LAL 1 gram 2 l6 BioTere AS-40 l milliliter 4 21 Potassium cocoate 1-ram _— Nacconol 90G 2 milliliter l 0 Table 10 shows the results from women’s bathroom testing on a variety of surfaces (floor, toilet bowl, and door handle), and the number of bacterial or fungal colonies swiped from the es with a Kimwipe that grew after 48 hours on a potato dextrose broth plate.

Verticillium Experiment Thirty pea seeds were inoculated with Verticillium sp. after being placed on a petri dish growing the . The seeds were rolled around liberally and then samples of the fungus were scraped up and placed with the pea seeds in a petri dish that was sealed with parafilm and left for three days. After the three days had , potato dextrose agar plates with sterilized caps placed in their centers were either filled with 50 microliters of 8-3, 20 microliters of 8-3, or left empty as a l. Ten pea seeds from the inoculated group were placed in each of the three petri dishes containing potato dextrose agar, and filled or unfilled caps. The peas were left for two days and then checked for fungal growth and germination. The results of the experiment are depicted in Table ll.

Table ll: Verticillium Inoculated Pea seeds Treatment Percent with Fun al Growth microliters 8-3 _ 50 microliters 8-3 _ The percent of pea seeds inoculated with illium sp. that ated and showed fungal growth after 48 hours in the control (no 8-3), with 20 microliters S-3, and with 50 microliters S- Camelina Experiment Camelina seeds known to be contaminated with various fungal and bacterial pathogens were taken and placed with S3 to see if fungal and bacterial growth could be halted. Several potato dextrose broth plates were obtained along with caps for 8-3 placement. About forty seeds were placed on one of the plates and an empty, sterilized cap was placed in the center as the control group. This plate was parafilmed and left for two days to determine germination and fungal and ial growth. Over one hundred seeds were placed on another petri dish with a sterilized cap filled with 50 microliters of S-3. These seeds were left to sit with the S-3 in a tightly parafilmed dish for the following hourly als, at which point twenty to thirty seeds were taken out and plated dually on a dish: 1 hours, 2 hours, 4 hours, 8 hours, 16 hours, 24 hours, and 48 hours. For each of the intervals, the plates were left for 48 hours and then checked for germination and en growth.

Table 12: Camelina Seeds Germination and Pathogen Growth Seeds Per Plate Percent Germinated Percent with Pathogen Growth Control 100 56 50 microliters S—3: —— 2 Hour 25 96 40 4 Hour Table 12 shows the number of infected camelina seeds’ percent germination and percent with pathogen growth that were either plated with no S-3 (control), or plated with 50 microliters of S- 3 at hourly intervals. All s were recorded 48 hours after being put on potato dextrose broth plates.

The disclosures of each and every patent, patent application, and publication cited herein are hereby incorporated herein by reference in their entirety.

While this ion has been disclosed with reference to specific embodiments, it is apparent that other embodiments and variations of this invention may be d by others skilled in the art without departing from the true spirit and scope of the invention. The appended claims are intended to be construed to include all such embodiments and equivalent variations.

Claims (21)

1. A chemical formulation having antimicrobial and antibacterial activity and comprising an antimicrobial component comprising an acid component including at least one of oic acid and isobutyric acid, and isoamyl ates.

2. The chemical formulation of claim 1, wherein the acid component includes both propanoic acid and isobutyric acid.

3. The formulation of claim 1 or 2, wherein the ratio of the acid component to isoamyl hexanoates is about 7:2 v/v.

4. The chemical formulation of claim 2, wherein the ratio of propanoic acid: isobutyric acid: isoamyl hexanoates is about 3.5:3.5:2 v/v/v.

5. A composition having antimicrobial and antibacterial activity and comprising the chemical formulation of any one of claims 1 to 4.

6. The composition of claim 5, wherein the composition is in a form of a , capsule, pill, gel cap, troche, dispersion, suspension, solution, syrup, granules, beads, transdermal patch, gel, powder, pellet, magma, lozenge, cream, paste, plaster, lotion, disc, itory, liquid spray for nasal or oral administration, dry powder or aerosolized formulation for inhalation, or oral rinse.

7. The composition of claim 6, wherein the composition is formulated so as to be suitable for ng human or animal waste.

8. The composition of claim 6, wherein the composition is formulated so as to be le for use as a human or animal nutritional ment.

9. The composition of claim 6, wherein the ition is formulated so as to be suitable for use in treating or preventing a pathogenic or wound infection.

10. The composition of claim 6, wherein the composition is formulated so as to be suitable for administration to a patient’s area in a hospital or home.

11. The ition of claim 6, wherein the composition is formulated so as to be suitable for administration to an animal’s bedding.

12. A disinfecting composition comprising the formulation of any one of claims 1 to 4.

13. The disinfecting composition of claim 12, wherein the composition is formulated so as to be suitable for ng microbial or bacterial growth on solid surfaces or instruments, or in areas.

14. The ecting composition of claim 13, where the solid surfaces, instruments, or areas are located in one or more locations selected from the following: a medical facility; an agricultural plant; a livestock ty; a hospital or other medical facility; a home or restaurant or grocery food ation area; an industrial food processing center; food processing center; and other locations where food is prepared, processed, stored, transported, or sold, and in which microbial or bacterial contamination may be a problem.

15. The disinfecting ition of claim 13, wherein the solid surface is located in a home, hospital, food processing center, food prep area, animal facility, medical facility, agricultural plant, livestock facility, or other location requiring cleaning or disinfection.

16. The disinfecting composition of any one of claims 12 to 15, formulated for administration which includes regular or periodic use of the composition.

17. Use of the chemical formulation or the chemical ition of any one of claims 1 to 9 in the manufacture of a ment for treating a disease or disorder ated with a ial or bacterial infection.

18. The use of claim 17, wherein the microbial or bacterial infection is caused by at least one of the ing: E. coli, S. aureus, and Salmonella.

19. A method of cleaning or disinfecting an inanimate surface, comprising using the composition of any one of claims 12 to 15.

20. A method of aminating, degrading, or deodorizing human or animal waste, comprising use of the formulation of any one of claims 5 to 7.

21. The method of claim 20, for treatment of waste in one or more locations selected from the following: a latrine, cat litter box, animal stall, barn, chicken-raising facility, pig barn, pet station in a home, and zoo.