CN119666810A - A method for fluorescence detection of Mycobacterium tuberculosis using tongue swab samples based on image processing - Google Patents
A method for fluorescence detection of Mycobacterium tuberculosis using tongue swab samples based on image processing Download PDFInfo
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Abstract
The invention discloses a method for detecting mycobacterium tuberculosis by tongue swab sample fluorescence based on image processing, which relates to the technical field of image processing and comprises a flora monitoring module, an image analysis module and a concentration determination module, wherein the flora monitoring module is used for identifying flora culture fluid and monitoring flora on the flora culture fluid in real time, the image analysis module is used for carrying out straight division processing on a shot image and fitting the outline of the flora, the concentration determination module is used for analyzing the size of the flora, the shape of the bifidobacterium and the life cycle in the image data and carrying out targeted fluorescent agent concentration adjustment on the flora with different growth conditions, and the flora monitoring module comprises an image monitoring unit and a flora culture fluid identification module, wherein the image monitoring unit is electrically connected with the flora culture fluid identification module and the flora identification module, and the flora culture fluid identification module is electrically connected with the flora identification module.
Description
Technical Field
The invention relates to the technical field of image processing, in particular to a method for detecting mycobacterium tuberculosis by tongue swab sample fluorescence based on image processing.
Background
The tongue swab sample fluorescence detection of the mycobacterium tuberculosis is a laboratory method for tuberculosis diagnosis, and the fluorescence detection technology can rapidly and sensitively identify the existence of the mycobacterium tuberculosis, so that early diagnosis of tuberculosis is realized. In the growth and division process of the mycobacterium tuberculosis, the absorption effect of the fluorescent agent is changed, the initial individuals of growth and division are small, the rod-shaped branching characteristics are not obvious, the quantity of the bacteria is increased along with rapid proliferation of the bacteria, the bacteria can show typical rod-shaped branching structures, and the division speed is slowed down along with apoptosis of the service life of the bacteria.
When the existing bifidobacterium flora is taken out of a culture room and observed for a growth experiment, fluorescent agents with the same concentration are uniformly added for coloring treatment, and the life cycle of the flora is different, and researches show that the life cycle of the flora is different, the concentration of the adaptive fluorescent agents is also different, and the absorption capacity of the bacterial flora on the fluorescent agents is reduced along with the continuation of the life cycle of the bacteria, so that more fluorescent agents are needed for better observation, and the bifidobacterium flora in the early stage of the life cycle can absorb excessive fluorescent agents to cause unclear detail observation. Therefore, it is necessary to design a method for detecting mycobacterium tuberculosis by real-time control based on image processing tongue swab sample fluorescence.
Disclosure of Invention
The invention aims to provide a method for detecting mycobacterium tuberculosis by tongue swab sample fluorescence based on image processing, so as to solve the problems in the background technology.
In order to solve the technical problems, the invention provides a method for detecting mycobacterium tuberculosis based on tongue swab sample fluorescence of image processing, which comprises a flora monitoring module, an image analysis module and a concentration determination module, wherein the flora monitoring module is used for identifying flora culture solution and monitoring flora on the flora culture solution in real time, the image analysis module is used for carrying out straight division processing on a shot image and fitting flora contours, and the concentration determination module is used for analyzing the flora size, the bifidobacterium shape and the life cycle in image data and carrying out targeted fluorescent agent concentration adjustment on flora with different growth conditions.
According to the technical scheme, the flora monitoring module comprises an image monitoring unit, a flora culture solution identification module and a flora identification module, wherein the image monitoring unit is electrically connected with the flora culture solution identification module and the flora identification module, and the flora culture solution identification module is electrically connected with the flora identification module;
The image monitoring unit is used for acquiring image data of the flora culture solution, the flora culture solution identification module is used for identifying the flora culture solution by utilizing an image identification technology and determining the flora culture solution grown by the flora, and the flora identification module is used for identifying the flora on the flora culture solution and determining the position of the flora in the flora culture solution;
The image analysis module comprises a coordinate establishment module, a growth area division module, a position marking module, a flora outline drawing module and an interval photographing module, wherein the interval photographing module is electrically connected with the position marking module, the position marking module is electrically connected with the flora outline drawing module, the coordinate establishment module is sequentially and electrically connected with the growth area division module and the position marking module, the coordinate establishment module is used for generating a culture area map of a monitored flora culture solution image, the growth area division module is used for intersecting the culture area map with straight lines and vertical lines according to the same interval size and setting boundaries of the intersecting points, the position marking module is used for recording point position coordinates of the flora image elements, the flora outline drawing module is used for identifying outlines of the flora images and drawing simplified flora outlines, and the interval photographing module is used for photographing and recording the images according to a certain period;
The concentration determining module comprises a time marking module, a flora size analyzing module, a growth speed calculating module, an individual shape judging module, a concentration calculating module and a weight determining module, wherein the time marking module is electrically connected with the growth speed calculating module, the growth speed calculating module is electrically connected with the concentration calculating module, and the flora size analyzing module and the individual shape judging module are electrically connected with the flora outline drawing module;
the time marking module is used for calculating time to serve as the basis of other data, the flora size analysis module is used for analyzing the position coordinates of flora image elements and the outline size of the flora, the growth speed calculation module is used for calculating the life cycle of the flora according to the change of the shape and the size of the image photographing record, the individual shape judgment module is used for judging the shape of the individual bifidobacteria in the flora by combining the image elements, the concentration calculation module is used for reducing the concentration of the flora which grows fast, and the weight decision module is used for adjusting the size of the flora and the influence weight of the individual shape on the life cycle of the flora according to the using time of the culture solution.
According to the technical scheme, the working method of the system comprises the following steps:
s1, taking the bifidobacteria and dividing the bifidobacteria into a plurality of parts with similar sizes, shooting the bifidobacteria flora with the same initial size by using an image monitoring unit, generating coordinates of all cross points to serve as growth positions of the flora, and counting the use time of the culture solution;
S2, photographing and recording the image information of the intersection according to a certain period, and not recording the image information at other times, and drawing the outline of the flora according to whether the image elements of the flora appear at the coordinate points;
S3, calculating the outline size of the flora by combining the outline scanning image of the flora to obtain the splitting speed of the flora, and analyzing the shape of the flora to obtain the growth stage of the flora;
s4, adjusting the weight of the shape of the bifidobacteria on the life cycle of the flora in combination with the use time of the culture solution, and calculating the life cycle of the flora;
S5, adjusting the concentration of the fluorescent agent according to the life cycle of the flora, so that the observation conditions of each flora are adjusted to be similar, and unified observation and comparison are facilitated.
According to the above technical scheme, in S3, the method for calculating the outline size of the flora includes:
S3-1, after the flora recognition module recognizes the flora outline, the flora outline drawing module is used for marking and locking pixel points in the shape edge of the flora picture, and smooth connection is carried out on adjacent pixel points, and the image grid takes the flora distance from the image monitoring unit as a reference distance The reference unit area at the time is;
S3-2, calculating the number of image grids of the outline surrounded by the smooth connecting linesThe image size of the flora is the image size, and the distance value is perceived by the distance of the imageQuantifying the flora propagation speed at the current distanceAt the same timeThe greater the speed of the splitting is the faster,The conversion coefficient of the image size and the propagation speed of the flora.
According to the above technical scheme, in S3, the specific method for analyzing the shape of the flora is as follows:
s3-3, the coordinates of the transverse extreme points of the individual bifidobacteria in the flora in the microscope picture are respectively And connecting the marked points to draw as a bifidobacterium midrace transverse drawing line;
s3-4, the coordinates of the longitudinal extreme points of the individual bifidobacteria in the flora in the microscope picture are respectively And connecting the marked points to draw as a longitudinal drawing line of the bifidobacterium middleyanum;
S3-5, performing shape analysis on all the individual bifidobacteria in the flora, and calculating the average rod-shaped divergence characteristic of the individual bifidobacteria in the flora, namely the growth stage value ,
,
,,,,,,,Are the coordinate values of the mark points,The larger the growth phase the closer to maturity.
According to the above technical scheme, in S4, the life cycle of the floraThe method for calculating is that the ratio of different stages of the bacterial colony development and the shape and size after maturation are different, the bacterial colony propagation speed and the bacterial colony growth stage valueNeither can fully accurately reflect the life cycle of the flora,Speed of propagation for floraAnd growth stage value of floraIs the integrated value of (1), i.e,Is a weight coefficient of the propagation speed of the flora,The weight coefficient of the bacterial colony in the growth stage is taken according to practical experience, and in the initial stage of using the bacterial in the culture solution,Maximally, with the continuous use of the culture solution,Will decrease in proportion to the time of use.
According to the above technical scheme, in S5, the method for adjusting the concentration of the fluorescent agent comprises setting an injection point for each coordinate point, and taking pictures at intervals according to the life cycle of the flora in the normal growth stage of the floraPreliminary setting of the concentration of the fluorescent agent, i.e. standard life cycle of the flora at different time points, is performedRespectively isThe standard concentration of the corresponding fluorescent agent is respectivelyWhen the life cycle of a certain floraBelow the corresponding point in timeWhen the concentration of the fluorescent agent is reducedOtherwise increase。
According to the above technical scheme, in S5, the specific calculation method of the concentration of the fluorescent agent is as follows: Wherein The concentration conversion coefficient of the fluorescent agent.
Compared with the prior art, the method has the beneficial effects that the splitting speed and the growth stage of the bifidobacterium flora are comprehensively counted through an image analysis method to obtain the life cycle of the flora, the two factors are comprehensively considered in the calculation method of the life cycle, the phenomenon of overlarge deviation caused by single judgment is avoided, and meanwhile, the concentration of the fluorescent agent is adjusted through the method, so that the life cycle which is as consistent as possible is convenient to observe accurately.
Drawings
The accompanying drawings are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate the invention and together with the embodiments of the invention, serve to explain the invention. In the drawings:
fig. 1 is a schematic view of the overall module structure of the present invention.
Detailed Description
The following description of the embodiments of the present invention will be made clearly and completely with reference to the accompanying drawings, in which it is apparent that the embodiments described are only some embodiments of the present invention, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Referring to fig. 1, the method for detecting mycobacterium tuberculosis based on tongue swab sample fluorescence of image processing comprises a flora monitoring module, an image analysis module and a concentration determination module, wherein the flora monitoring module is used for identifying flora culture solution and monitoring flora on the flora culture solution in real time, the image analysis module is used for carrying out straight division processing on photographed images and fitting flora contours, and the concentration determination module is used for analyzing the size of the flora, the shape of the bifidobacterium and the life cycle in image data and carrying out targeted fluorescent agent concentration adjustment on the flora with different growth conditions;
the flora monitoring module comprises an image monitoring unit, a flora culture solution identification module and a flora identification module, wherein the image monitoring unit is electrically connected with the flora culture solution identification module and the flora identification module, and the flora culture solution identification module is electrically connected with the flora identification module;
The image monitoring unit is used for acquiring image data of the flora culture solution, the flora culture solution identification module is used for identifying the flora culture solution by utilizing an image identification technology and determining the flora culture solution grown by the flora, and the flora identification module is used for identifying the flora on the flora culture solution and determining the position of the flora in the flora culture solution;
The image analysis module comprises a coordinate establishment module, a growth area division module, a position marking module, a flora outline drawing module and an interval photographing module, wherein the interval photographing module is electrically connected with the position marking module, the position marking module is electrically connected with the flora outline drawing module, the coordinate establishment module is sequentially electrically connected with the growth area division module and the position marking module, the coordinate establishment module is used for generating a culture area map of a monitored flora culture solution image, the growth area division module is used for intersecting the culture area map with a straight line and a vertical line according to the same interval size and setting the boundary of the intersection point, the position marking module is used for recording the point position coordinates of the flora image elements, the flora outline drawing module is used for identifying the outline of the flora image, drawing a simplified flora outline, and the interval photographing module is used for photographing and recording the image according to a certain period;
The concentration determining module comprises a time marking module, a flora size analyzing module, a growth speed calculating module, an individual shape judging module, a concentration calculating module and a weight determining module, wherein the time marking module is electrically connected with the growth speed calculating module, the growth speed calculating module is electrically connected with the concentration calculating module, and the flora size analyzing module and the individual shape judging module are electrically connected with the flora outline drawing module;
The time marking module is used for calculating time as the basis of other data, the flora size analysis module is used for analyzing the position coordinates of flora image elements and the outline size of the flora, the growth speed calculation module is used for calculating the life cycle of the flora according to the changes of the shape and the size of the image photographing record, the individual shape judgment module is used for judging the shape of the individual bifidobacteria in the flora by combining the image elements, the concentration calculation module is used for reducing the concentration of the flora which grows fast, and the weight decision module is used for adjusting the size of the flora and the influence weight of the shape of the individual on the life cycle of the flora according to the using time of the culture solution;
The working method of the system comprises the following steps:
s1, taking the bifidobacteria and dividing the bifidobacteria into a plurality of parts with similar sizes, shooting the bifidobacteria flora with the same initial size by using an image monitoring unit, generating coordinates of all cross points to serve as growth positions of the flora, and counting the use time of the culture solution;
S2, photographing and recording the image information of the intersection according to a certain period, and not recording the image information at other times, and drawing the outline of the flora according to whether the image elements of the flora appear at the coordinate points;
S3, calculating the outline size of the flora by combining the outline scanning image of the flora to obtain the splitting speed of the flora, and analyzing the shape of the flora to obtain the growth stage of the flora;
s4, adjusting the weight of the shape of the bifidobacteria on the life cycle of the flora in combination with the use time of the culture solution, and calculating the life cycle of the flora;
s5, adjusting the concentration of the fluorescent agent according to the life cycle of the flora, so that the observation conditions of each flora are adjusted to be similar, and unified observation and comparison are facilitated;
in S3, the method for calculating the outline size of the flora comprises the following steps:
S3-1, after the flora recognition module recognizes the flora outline, the flora outline drawing module is used for marking and locking pixel points in the shape edge of the flora picture, and smooth connection is carried out on adjacent pixel points, and the image grid takes the flora distance from the image monitoring unit as a reference distance The reference unit area at the time is;
S3-2, calculating the number of image grids of the outline surrounded by the smooth connecting linesThe image size of the flora is the image size, and the distance value is perceived by the distance of the imageQuantifying the flora propagation speed at the current distanceAt the same timeThe greater the speed of the splitting is the faster,Conversion coefficient for image size and propagation speed of flora;
s3, a specific method for analyzing the shape of the flora comprises the following steps:
s3-3, the coordinates of the transverse extreme points of the individual bifidobacteria in the flora in the microscope picture are respectively And connecting the marked points to draw as a bifidobacterium midrace transverse drawing line;
s3-4, the coordinates of the longitudinal extreme points of the individual bifidobacteria in the flora in the microscope picture are respectively And connecting the marked points to draw as a longitudinal drawing line of the bifidobacterium middleyanum;
S3-5, performing shape analysis on all the individual bifidobacteria in the flora, and calculating the average rod-shaped divergence characteristic of the individual bifidobacteria in the flora, namely the growth stage value ,
,
,,,,,,,Are the coordinate values of the mark points,The larger the growth phase, the closer to maturity;
s4, life cycle of flora The method for calculating is that the flora propagation speed is improved due to different ratio of flora at different stages of development and different shape and size after maturationAnd growth stage value of floraNeither can fully accurately reflect the life cycle of the flora,Speed of propagation for floraAnd growth stage value of floraIs the integrated value of (1), i.e,Is a weight coefficient of the propagation speed of the flora,The weight coefficient of the bacterial colony in the growth stage is taken according to practical experience, and in the initial stage of using the bacterial in the culture solution,Maximally, with the continuous use of the culture solution,Will decrease in proportion to the time of use;
S5, setting an injection point for each coordinate point, and taking pictures at intervals according to the life cycle of the flora in the normal growth stage of the flora Preliminary setting of the concentration of the fluorescent agent, i.e. standard life cycle of the flora at different time points, is performedRespectively isThe standard concentration of the corresponding fluorescent agent is respectivelyWhen the life cycle of a certain floraBelow the corresponding point in timeWhen the concentration of the fluorescent agent is reducedOtherwise increase;
In S5, the specific calculation method of the concentration of the fluorescent agent comprises the following steps: Wherein The concentration conversion coefficient of the fluorescent agent.
It is noted that relational terms such as first and second, and the like are used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Moreover, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus.
It should be noted that the above-mentioned embodiments are merely preferred embodiments of the present invention, and the present invention is not limited thereto, but may be modified or substituted for some of the technical features thereof by those skilled in the art. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention should be included in the protection scope of the present invention.
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101273016A (en) * | 2005-07-28 | 2008-09-24 | 詹森药业有限公司 | Antibacterial quinoline derivatives |
| JP2008304298A (en) * | 2007-06-07 | 2008-12-18 | Panasonic Corp | Bacteria discrimination device and bacteria discrimination method |
| CN101925819A (en) * | 2007-12-28 | 2010-12-22 | 株式会社比尔生命 | Immune detection method for Mycobacterium tuberculosis complex |
| CN115187620A (en) * | 2022-07-07 | 2022-10-14 | 湖南省结核病防治所(湖南省胸科医院) | Method and system for detecting concentration of bifidobacterium |
| CN118845083A (en) * | 2024-07-03 | 2024-10-29 | 复旦大学附属华山医院 | A medical digital imaging system and method for urology |
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Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101273016A (en) * | 2005-07-28 | 2008-09-24 | 詹森药业有限公司 | Antibacterial quinoline derivatives |
| JP2008304298A (en) * | 2007-06-07 | 2008-12-18 | Panasonic Corp | Bacteria discrimination device and bacteria discrimination method |
| CN101925819A (en) * | 2007-12-28 | 2010-12-22 | 株式会社比尔生命 | Immune detection method for Mycobacterium tuberculosis complex |
| CN115187620A (en) * | 2022-07-07 | 2022-10-14 | 湖南省结核病防治所(湖南省胸科医院) | Method and system for detecting concentration of bifidobacterium |
| CN118845083A (en) * | 2024-07-03 | 2024-10-29 | 复旦大学附属华山医院 | A medical digital imaging system and method for urology |
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Application publication date: 20250321 |