Method and kit for detecting the presence and / or abundance of bacteria in food, beverage, environmental, or biological samples

Abstract

Provided is a method that makes it possible to detect the presence and / or amount of bacteria in a food / drink sample, environmental sample, or biological sample in a short period of time, simply, and efficiently. This method comprises a step in which the presences and / or amounts of bacteria of two or more different genera in a sample are simultaneously detected on the basis of antigen-antibody reactions.

Description

[Technical field]

[0001] The present invention relates to methods and kits for detecting the presence and / or abundance of bacteria in a food or beverage, environmental, or biological sample. [Background technology]

[0002] Conventional methods for detecting the presence or absence or amount of bacteria in food and beverage samples, environmental samples, or biological samples, or for determining the degree of bacterial contamination, include the culture method in which the sample is cultured and the growth of bacteria is confirmed (e.g., Patent Document 1: JP 63-233774 A; Patent Document 2: WO 2019 / 142848 A), and the ATP method in which intracellular ATP (adenosine triphosphate) of bacteria in the sample is detected (e.g., Patent Document 3: JP 11-239493 A; Patent Document 4: JP 2009-136205 A).

[0003] However, conventional culture methods require culture equipment and take several days to a week until detection, posing problems in terms of testing location, effort, and time. Another problem is that only specific bacteria that match the culture conditions (medium components, aerobic / anaerobic atmosphere, set temperature, etc.) grow, and a wide range of bacterial genera cannot be detected simultaneously. Another problem with conventional ATP methods is that ATP is present not only in bacterial cells but also in eukaryotic cells (animal cells, plant cells), making it difficult to distinguish bacteria from eukaryotic cells derived from food, beverages, and the environment.

[0004] In actual situations where it is necessary to detect the presence or absence and / or amount of bacteria in food and beverage samples, environmental samples, or biological samples, there are situations where it is necessary to comprehensively and quickly detect multiple genera of bacteria (e.g., detection of total bacterial count, general bacterial count, coliform bacteria, Enterobacteriaceae group), rather than detecting various bacteria individually, such as bacterial tests in the sanitation management of food and beverages and the environment. Therefore, if there is a method that can detect multiple genera of bacteria present in food and beverages, the environment, living organisms, etc. at the same time, it would be of great technical significance and usefulness. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Japanese Patent Application Publication No. 63-233774 [Patent Document 2] International Publication No. 2019 / 142848 [Patent Document 3] Japanese Patent Application Publication No. 11-239493 [Patent Document 4] JP 2009-136205 A Summary of the Invention [Problem to be solved by the invention]

[0006] One aspect of the present invention aims to provide a method and kit capable of detecting the presence or absence and / or amount of bacteria in a sample such as a food or beverage sample, an environmental sample, or a biological sample in a short period of time, simply and efficiently. [Means for solving the problem]

[0007] As a result of intensive research, the present inventors have come up with the idea that the presence / absence and / or abundance of bacteria of different genera in a sample can be detected simply and efficiently in a short time by simultaneously detecting the presence / absence and / or abundance of bacteria of different genera in a sample based on an antigen-antibody reaction. In addition, the present inventors have come up with the idea that the presence / absence and / or abundance of bacteria of different genera in a sample can be detected simply and efficiently in a short time by using a general-purpose antibody that undergoes a broad antigen-antibody reaction with various bacteria in combination with one or more specific antibodies that undergo a specific antigen-antibody reaction with a specific bacterium. Based on this idea, the present inventors have actually produced antibodies that undergo an antigen-antibody reaction with bacteria of different genera, and demonstrated that the presence / absence and / or abundance of bacteria of different genera in a sample can be detected simply and efficiently in a short time by using these antibodies, thereby arriving at the present invention.

[0008] That is, the gist of the present invention is as follows. [Item 1] A method for detecting the presence and / or amount of bacteria in a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method comprises a step of simultaneously detecting the presence or absence and / or amount of bacteria of at least two or more different genera in a sample based on an antigen-antibody reaction. [Item 2] The method according to Item 1, wherein in the detection step, bacteria of two or more different genera selected from the group consisting of the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella are simultaneously detected. [Item 3] The method according to Item 1 or 2, wherein the two or more genera of bacteria to be detected include both gram-negative bacteria and gram-positive bacteria. [Item 4] The method according to any one of Items 1 to 3, wherein in the detection step, bacteria of at least 3 or more, or 4 or more, or 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, or 10 or more, or 11 or more different genera are simultaneously detected. [Item 5] The method according to any one of Items 1 to 4, wherein the detection step includes a step of contacting a specimen with an antibody that undergoes an antigen-antibody reaction with a component derived from the two or more genera of bacteria, and a step of measuring the presence or absence and / or strength of the antigen-antibody reaction that occurs in the specimen after the contact. [Item 6] The method described in Item 5, wherein the antibody is an antibody that generates an antigen-antibody reaction with ribosomal protein L7 / L12 of bacteria of the two or more genera. [Item 7] The method according to Item 5 or 6, further comprising a step of lysing bacteria in the sample before contacting the antibody with the sample. [Item 8] The method according to any one of Items 5 to 7, wherein the antibody does not cross-react with one or more non-bacteria-derived components that may be present in a sample. [Item 9] The method according to Item 8, wherein the non-bacteria-derived components that do not cross-react with the antibody are organic components derived from viruses, plants, and / or animals. [Item 10] The method according to any one of Items 5 to 9, wherein the antibody is a monoclonal antibody or a fragment thereof, or a derivative thereof. [Item 11] The monoclonal antibody or a fragment thereof, or a derivative thereof, As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5, and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6 Item 11. The method according to item 10, each of which comprises: [Item 12] The monoclonal antibody or a fragment thereof, or a derivative thereof, A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 1, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 2, or A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 3, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 4, or The heavy chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:5, and the light chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:6. Item 12. The method according to item 11. [Item 13] The method according to any one of items 5 to 12, comprising: (I) capturing and labeling bacteria in the specimen through an antigen-antibody reaction between the specimen, a capture antibody linked to a solid phase carrier, and a detection antibody having a detection label; and (II) A step of detecting the target bacteria in the sample based on the detection marker. detecting the presence and / or amount of bacteria in a sample by One of the capture antibody and the detection antibody is one or more specific antibodies that undergo an antigen-antibody reaction with one or more types of target bacteria, and the other antibody is one or more general antibodies that undergo an antigen-antibody reaction with five or more genera of bacteria including the target bacteria, and The method, wherein either the general antibody or the specific antibody is the antibody according to any one of items 5 to 12. [Section 14] The step (I) is (Ia-1) contacting a specimen with a detection antibody and labeling the bacteria in the specimen by an antigen-antibody reaction between the detection antibody and the bacteria; and (Ia-2) A step of contacting a specimen containing bacteria labeled with a detection antibody with a capture antibody and capturing the bacteria in the specimen by an antigen-antibody reaction between the capture antibody and the bacteria-detection antibody complex. Item 14. The method according to item 13, comprising: [Section 15] The step (I) is (Ib-1) contacting a specimen with a capture antibody and capturing bacteria in the specimen through an antigen-antibody reaction between the capture antibody and the bacteria; and (Ib-2) A step of contacting a specimen containing the bacteria captured by the capture antibody with a detection antibody, and labeling the bacteria in the specimen by an antigen-antibody reaction between the detection antibody and the bacteria-capture antibody complex. Item 14. The method according to item 13, comprising: [Item 16] The method according to any one of Items 13 to 15, wherein the capture antibody is a general-purpose antibody and the detection antibody is a specific antibody. [Item 17] The method according to any one of Items 13 to 15, wherein the detection antibody is a general-purpose antibody and the capture antibody is a specific antibody. [Item 18] The method according to any one of Items 13 to 17, wherein the generic antibody undergoes an antigen-antibody reaction with bacteria of five or more genera selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella. [Item 19] The method according to any one of Items 13 to 18, wherein the specific antibody specifically reacts with bacteria of one or more genera selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella. [Item 20] A universal antibody, As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5, and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6 20. The method according to any one of items 13 to 19, each of which comprises: [Item 21] A universal antibody, A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 1, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 2, or A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 3, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 4, or The heavy chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:5, and the light chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:6. 21. The method according to item 20. [Item 22] A specific antibody, As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, and SEQ ID NO: 13, and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, and SEQ ID NO: 14. 22. The method according to any one of items 13 to 21, each of which comprises: [Item 23] A specific antibody, A heavy chain variable region sequence having an amino acid sequence having 80% or more homology to the amino acid sequence of SEQ ID NO: 7, and a light chain variable region sequence having an amino acid sequence having 80% or more homology to the amino acid sequence of SEQ ID NO: 8, or A heavy chain variable region sequence having an amino acid sequence having 80% or more homology to the amino acid sequence of SEQ ID NO: 9, and a light chain variable region sequence having an amino acid sequence having 80% or more homology to the amino acid sequence of SEQ ID NO: 10, or A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 11, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 12, or The heavy chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 13, and the light chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 14. 23. The method according to item 22. [Item 24] A method for determining the degree of bacterial contamination of a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method comprises a step of simultaneously detecting the presence or absence and / or the amount of bacteria of at least two or more genera in the sample based on an antigen-antibody reaction by the method according to any one of items 1 to 23. [Item 25] A kit for detecting the presence or absence and / or amount of bacteria in a sample selected from a food or drink sample, an environmental sample, and a biological sample by the method according to any one of items 5 to 12, the kit comprising the antibody according to any one of items 5 to 12. [Item 26] A kit for detecting the presence or absence and / or amount of bacteria in a sample selected from a food or drink sample, an environmental sample, and a biological sample by the method according to any one of items 13 to 23, the kit comprising a capture antibody and a detection antibody according to any one of items 13 to 23, one of the capture antibody and the detection antibody being the general-purpose antibody and the other being the specific antibody. [Item 27] ​​The method further comprises: developing a sample and contacting the sample with a capture antibody; A detection line having a capture antibody immobilized thereon is provided on the carrier, Item 27. The kit according to item 26, configured to detect two or more types of bacteria in a sample with a single detection line. [Item 28] The kit according to Item 26 or 27, wherein the kit is an immunochromatography kit. [Item 29] The capture antibody and the detection antibody are selected so as to undergo an antigen-antibody reaction with the ribosomal protein L7 / L12 of the bacteria in the sample to be detected, thereby forming a sandwich structure; The immunochromatography kit includes an insoluble membrane carrier for developing a sample and contacting the sample with a capture antibody, and a conjugate pad provided on the insoluble membrane carrier and having the detection antibody attached thereto, Item 29. The kit according to Item 28, wherein the capture antibody is immobilized in the chromatographic development direction relative to the conjugate pad on the insoluble membrane carrier. [Item 30] A method for producing the immunochromatography kit according to item 29, laminating the conjugate pad having the detection antibody attached thereto on the insoluble membrane carrier; and immobilizing the capture antibody in the chromatographic direction relative to the conjugate pad on the insoluble membrane carrier; A manufacturing method comprising at least the steps of: [Item 31] The manufacturing method described in Item 30, wherein the specific antibody is used as the capture antibody and the general antibody is used as the detection antibody. [Item 32] The production method described in Item 30 or 31, wherein the specific antibody is an antibody that specifically generates an antigen-antibody reaction with the target bacteria of one or more genera selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella. [Item 33] The method according to any one of Items 30 to 32, wherein the generic antibody specifically undergoes an antigen-antibody reaction with five or more target bacteria selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella. Effect of the Invention

[0009] According to the method of the present invention, it is possible to easily and efficiently detect the presence or absence and / or amount of bacteria in a food or drink sample, an environmental sample, or a biological sample in a short period of time. [Brief description of the drawings]

[0010] [Figure 1] FIG. 1 is a cross-sectional view showing a schematic configuration of a strip-shaped detection mechanism, which is an example of the detection mechanism of a lateral flow type immunochromatographic detection device. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0011] The present invention will be described in detail below with reference to specific embodiments. However, the present invention is not limited to the following embodiments, and can be embodied in any form without departing from the spirit of the present invention.

[0012] All documents cited in this specification, including patent publications, published patent applications, and non-patent publications, are hereby incorporated by reference in their entirety for all purposes.

[0013] In addition, in the formulas representing amino acid sequences described herein, amino acids are represented by single-letter codes unless otherwise specified.

[0014] One aspect of the present invention relates to a method for detecting the presence or absence and / or amount of bacteria in a food or beverage sample, an environmental sample, or a biological sample (hereinafter referred to as "the method of the present invention" as appropriate). The method of the present invention involves simultaneously detecting the presence or absence and / or amount of bacteria of multiple genera in a sample based on an antigen-antibody reaction. According to one aspect, such detection based on an antigen-antibody reaction is performed, for example, by contacting the sample with an antibody (hereinafter referred to as "the antibody of the present invention" as appropriate) that undergoes an antigen-antibody reaction with components derived from bacteria of multiple genera in the sample, and measuring the presence or absence and / or strength of the antigen-antibody reaction occurring in the sample after contact. By using the method of the present invention, for example, it becomes possible to easily and efficiently determine the degree of bacterial contamination of a food or beverage sample, an environmental sample, or a biological sample in a short period of time.

[0015] Furthermore, a kit containing the antibody of the present invention (kit of the present invention) for carrying out the method of the present invention is also within the scope of the present invention.

[0016] Below, we will first explain the method of the present invention, then explain the antibody of the present invention used in the method of the present invention, followed by an explanation of a particularly preferred embodiment of the method of the present invention (method (2) of the present invention), and then explain the kit used in the method of the present invention.

[0017] [1. Method for detecting the presence and / or amount of bacteria in a specimen (1)] The method of the present invention is a method for detecting the presence or absence and / or the amount of bacteria in a sample selected from food and drink samples, environmental samples, and biological samples. The method of the present invention includes simultaneously detecting the presence or absence and / or the amount of bacteria of multiple genera in a sample based on an antigen-antibody reaction. The method of the present invention may be used to determine, for example, the degree of bacterial contamination of the sample.

[0018] Examples of specimens include food and beverage specimens, environmental specimens, and biological specimens (hereinafter, food and beverage specimens and environmental specimens may be collectively abbreviated as "food and beverage / environmental specimens", and food and beverage specimens, environmental specimens, and biological specimens may be collectively abbreviated as "food and beverage / environmental / biological specimens"). There are no particular limitations on the type of food and beverage specimen, but examples include specimens obtained from ingredients such as meat, fish, vegetables, prepared foods, processed foods and beverages, and seasonings, as well as beverages such as water, tea, coffee, juice, and alcoholic beverages. The type of environmental sample is not particularly limited, but examples include samples obtained by wiping the surfaces of hands, work clothes, work shoes, nail brushes, cutting boards, knives, handles, conveyor belts, packaging materials, work desks, beds, faucets, showers, medical instruments, etc. in environments such as food and beverage manufacturing equipment, food and beverage service sites, medical equipment, and medical sites with collection tools (swabs) such as clean cotton or clean cloth impregnated with a liquid medium (water, physiological isotonic solution, ethanol, etc.), and liquid samples such as tap water, well water, river water, and hot spring water. The type of biological sample is not particularly limited, but examples include samples derived from humans or non-human animals such as whole blood, serum, plasma, urine, stool, hands, saliva, sputum, sweat, nasal mucus, throat swabs, nasal aspirates, and lung lavage fluid. Such food and beverage, environmental, and biological samples may be contaminated by a wide variety of bacteria.

[0019] As mentioned above, in order to detect bacterial contamination in such food and beverage, environmental, and biological samples, it was previously necessary to use the culture method or the ATP method. However, the culture method requires culture equipment and complicated culture work, takes several days to a week until detection, and can only detect specific bacteria that meet the culture conditions. Since the ATP method is also present in eukaryotic cells (animal cells, plant cells), it was difficult to distinguish bacteria from eukaryotic cells derived from food and beverage, the environment, and living organisms.

[0020] In the method of the present invention, the presence or absence and / or the amount of bacteria of multiple genera in a sample is simultaneously detected based on an antigen-antibody reaction. In the present invention, "antigen-antibody reaction" refers to an antibody specifically binding to its antigen. By using an antigen-antibody reaction, it is possible to detect the presence or absence and / or the amount of bacteria in a sample in real time on-site with simple equipment and operations. In the present invention, "simultaneous" detection of multiple types or multiple genera of bacteria means detecting multiple types or multiple genera of bacteria collectively, and is not necessarily limited to detecting them simultaneously in time. In addition, "simultaneous" detection of bacteria of two or more genera includes not only a mode in which bacteria of two or more genera are finally detected, but also a mode in which detection is performed using an antibody (i.e., a general-purpose antibody described later) that causes an antigen-antibody reaction with bacteria of two or more genera collectively (i.e., "simultaneously") even if the bacteria finally detected are of a single genus. In the present invention, by appropriately selecting and using antibodies (antibodies of the present invention) that specifically undergo antigen-antibody reactions with components derived from multiple genera of bacteria to be detected, it becomes possible to simultaneously detect multiple genera of bacteria to be detected, reduce false positives due to components other than bacteria, and improve detection sensitivity and detection accuracy. As a result, it becomes possible to easily and efficiently determine the degree of contamination of a sample by multiple genera of bacteria in a short time.

[0021] Bacteria that can be detected by the method of the present invention include bacteria belonging to the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella (hereinafter referred to as "specific bacterial genera"), which are representative bacterial genera that are in high demand for detection in foods, beverages, the environment, and biological samples. In the method of the present invention, it is preferable to detect antigen-antibody reactions with bacteria from at least two or more genera (multiple genera) of these specific bacterial genera, and it is particularly preferable to detect antigen-antibody reactions with bacteria from at least three or more, or four or more, or five or more, or six or more, or seven or more, or eight or more, or nine or more, or ten or more genera, and particularly preferably all of the eleven specific bacterial genera.

[0022] Examples of bacteria of the genus Escherichia include Escherichia coli (E. coli, EC), Escherichia albertii (E. albertii), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Escherichia, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Escherichia coli.

[0023] Examples of bacteria of the genus Staphylococcus include Staphylococcus aureus (S. aureus, SA), Staphylococcus epidermidis (S. epidermidis), Staphylococcus argenteus (S. argenteus), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Staphylococcus, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Staphylococcus aureus.

[0024] Examples of bacteria of the genus Pseudomonas include Pseudomonas aeruginosa (P. aeruginosa, PA), Pseudomonas fluorescens (P. fluorescens), Pseudomonas phosphorescence (P. phosphorescence), Pseudomonas putida (P. putida), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Pseudomonas, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Pseudomonas aeruginosa.

[0025] Examples of bacteria of the genus Bacillus include Bacillus subtilis (B. subtilis, BS), Bacillus cereus (B. cereus), Bacillus licheniformis (B. licheniformis), Bacillus megaterium (B. megaterium), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Bacillus, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Bacillus subtilis.

[0026] Examples of bacteria belonging to the genus Klebsiella include Klebsiella pneumoniae (K. pneumoniae, KP), Klebsiella oxytoca (K. oxytoca), Klebsiella aerogenes (K. aerogenes), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria belonging to the genus Klebsiella, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Klebsiella pneumoniae.

[0027] Examples of bacteria of the genus Serratia include Serratia liquefaciens (S. liquefaciens, SL), Serratia marcescens (S. marcescens), Serratia fonticola (S. fonticola), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Serratia, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Serratia liquefaciens.

[0028] Examples of bacteria of the genus Rahnella include Rahnella aquatilis (R. aquatilis, RA), Rahnella victoriana (R. victoriana), Rahnella bruchi (R. bruchi), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Rahnella, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Rahnella aquatilis.

[0029] Examples of bacteria of the genus Citrobacter include Citrobacter freundii (C. freundii, CF), Citrobacter amalonaticus (C. amalonaticus), Citrobacter diversus (C. diversus), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Citrobacter, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Citrobacter freundii.

[0030] Examples of bacteria of the genus Listeria include Listeria monocytogenes (L. monocytogenes, LM), Listeria innocua (L. innocua), Listeria ivanovii (L. ivanovii), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Listeria, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Listeria monocytogenes.

[0031] Examples of bacteria belonging to the genus Enterobacter include Enterobacter cloacae (E. cloacae, ECL), Enterobacter aerogenes (E. aerogenes), Enterobacter sakazakii (E. sakazakii), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria belonging to the genus Enterobacter, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Enterobacter cloacae.

[0032] Examples of bacteria of the genus Salmonella include Salmonella enteritidis (S. enteritidis, SE), Salmonella infantis (S. infantis), Salmonella typhimurium (S. typhimurium), etc. When the method of the present invention detects an antigen-antibody reaction with bacteria of the genus Salmonella, it is sufficient to detect an antigen-antibody reaction with any one or more of these bacteria, but it is preferable to detect an antigen-antibody reaction with at least Salmonella enteritidis.

[0033] In addition to the aforementioned bacteria, examples of genera of bacteria that can be detected by the method of the present invention include, but are not limited to, the genera Enterococcus, Moraxella, Aeromonas, Lactobacillus, Micrococcus, Acinetobacter, Campylobacter, Proteus, and Vibrio.

[0034] According to one embodiment of the present invention, bacteria to be detected may include bacteria belonging to the family Enterobacteriaceae (hereinafter referred to as "Enterobacteriaceae bacteria"). Examples of Enterobacteriaceae bacteria that are particularly required to be detected in this embodiment include, but are not limited to, Enterobacteriaceae bacteria belonging to the genera Escherichia, Klebsiella, Citrobacter, Enterobacter, Proteus, Salmonella, and Serratia, which are representative Enterobacteriaceae genera that are particularly required to be detected in foods, beverages, and the environment. Other Enterobacteriaceae bacteria that can be detected in this embodiment include, but are not limited to, Enterobacteriaceae bacteria belonging to the genera Yersinia, Erwinia, Hafnia, Morganella, Obessambacterium, Providencia, Shigella, Aeromonas, and Pectobacterium.

[0035] In one embodiment, it is preferable that the bacteria of multiple genera to be detected include both gram-negative and gram-positive bacteria, because the structures of the cell membrane and cell wall of the two bacteria are significantly different, making it difficult to simultaneously detect both bacteria with conventional techniques, but the method of the present invention makes it possible to simultaneously detect gram-negative and gram-positive bacteria by appropriately designing the antibodies used for detection.

[0036] According to the method of the present invention, the presence or absence and / or amount of bacteria in food, beverage, environmental, or biological specimens can be simultaneously detected based on an antigen-antibody reaction, making it possible to detect the presence or absence and / or amount of bacteria in a specimen in a short time, easily, and efficiently, as compared with the conventional culture method and ATP method. Furthermore, by using the method of the present invention, for example, it becomes possible to determine the degree of bacterial contamination of food, beverage, environmental, or biological specimens much more quickly and easily.

[0037] [2. Antibodies that react with components derived from multiple genera of bacteria in a specimen] In the method of the present invention, the method of simultaneously detecting the presence or absence and / or the amount of bacteria of multiple genera in a sample based on an antigen-antibody reaction is not particularly limited. According to one embodiment, such detection based on the antigen-antibody reaction is suitably carried out by contacting the sample with an antibody (the antibody of the present invention) that undergoes an antigen-antibody reaction with a component derived from bacteria of multiple genera, and measuring the presence or absence and / or the strength of the antigen-antibody reaction that occurs in the sample after the contact. The antibody of the present invention will be described below.

[0038] In the present invention, an "antibody" refers to a protein that recognizes and binds to a specific antigen or substance, and is sometimes called immunoglobulin (Ig). A typical antibody usually has two light chains and two heavy chains that are mutually bonded by disulfide bonds. There are two types of light chains, called λ chains and κ chains, and there are five types of heavy chains, called γ chains, μ chains, α chains, δ chains, and ε chains. Depending on the type of heavy chain, there are five isotypes of antibodies, called IgG, IgM, IgA, IgD, and IgE.

[0039] Each heavy chain contains a heavy chain constant (CH) region and a heavy chain variable (VH) region. Each light chain contains a light chain constant (CL) region and a light chain variable (VL) region. The light chain constant (CL) region is composed of a single domain. The heavy chain constant (CL) region is composed of three domains, namely CH1, CH2 and CH3. Each light chain variable (VL) region and heavy chain variable (VH) region are composed of four highly conserved regions (FR-1, FR-2, FR-3, FR-4) called framework regions (FR) and three hypervariable regions (CDR-1, CDR-2, CDR-3) called complementarity determining regions (CDR). The heavy chain constant (CH) region has three CDRs (CDR-H1, CDR-H2, CDR-H3) and four FRs (FR-H1, FR-H2, FR-H3, FR-H4), which are arranged from the amino terminus to the carboxy terminus in the following order: FR-H1, CDR-H1, FR-H2, CDR-H2, FR-H3, CDR-H3, FR-H4. The light chain constant (CL) region has three CDRs (CDR-L1, CDR-L2, CDR-L3) and four FRs (FR-L1, FR-L2, FR-L3, FR-L4), which are arranged from the amino terminus to the carboxy terminus in the following order: FR-L1, CDR-L1, FR-L2, CDR-L2, FR-L3, CDR-L3, FR-L4. The variable regions of the heavy and light chains contain binding domains that interact with antigens.

[0040] The antibody of the present invention may be a polyclonal antibody or a monoclonal antibody, but is preferably a monoclonal antibody. A polyclonal antibody is usually prepared from the serum of an animal immunized with an antigen, and is a mixture of various antibody molecular species with different structures. On the other hand, a monoclonal antibody refers to an antibody consisting of a single type of molecule containing a combination of a light chain variable (VL) region and a heavy chain variable (VH) region having a specific amino acid sequence. A monoclonal antibody can be produced from a clone derived from an antibody-producing cell, but it can also be produced by genetic engineering using a nucleic acid molecule obtained having a gene sequence that codes for the amino acids of the antibody protein. In addition, modification to improve the binding and specificity of an antibody using genetic information such as heavy and light chains, or their variable regions and CDRs, is a technique well known to those skilled in the art in this field.

[0041] The antibody of the present invention may be an antibody fragment and / or derivative. Examples of antibody fragments include F(ab')2, Fab, Fv, etc. Examples of antibody derivatives include antibodies in which amino acid mutations have been artificially introduced into the constant region of the light chain and / or heavy chain, antibodies in which the domain configuration of the constant region of the light chain and / or heavy chain has been modified, antibodies having two or more Fc regions per molecule, sugar chain-modified antibodies, bispecific antibodies, antibody conjugates in which an antibody or an antibody fragment is bound to a protein other than an antibody, antibody enzymes, tandem scFvs, bispecific tandem scFvs, diabodies, etc. Furthermore, when the antibody or a fragment or derivative thereof is derived from a non-human animal, the antibody of the present invention also includes chimeric antibodies or humanized antibodies in which a part or all of the sequence other than the CDR is replaced with the corresponding sequence of a human antibody. Unless otherwise specified, the term "antibody" in the present invention also includes antibody fragments and / or derivatives.

[0042] The antibody of the present invention causes an antigen-antibody reaction with a certain bacterium means that the antibody specifically binds to a certain component of the bacterium as an antigen. The bacterial component that serves as an antigen for the antibody of the present invention is not limited. It may be a component contained in the cell wall or cell membrane exposed outside the bacterial cell, or a component contained in the cytoplasm, organelles, nucleus, etc. that is not exposed outside the bacterial cell. When the antibody of the present invention causes an antigen-antibody reaction with a component that is not exposed outside the bacterial cell, in order to cause an antigen-antibody reaction between the antibody of the present invention and such a bacterial component, the sample may be subjected to a treatment to lyse the bacteria before contacting the antibody of the present invention with a food, drink, environment, or biological sample. Such a bacterial lysis treatment will be described later.

[0043] The antibody of the present invention is capable of detecting at least the following bacteria: Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, It is preferable that the antibody reacts with bacteria of 5 or more, 6 or more, 7 or more, 8 or more, 9 or more, 10 or more, or 11 or more genera selected from the genera Enterobacter and Salmonella. Specific bacterial species of these genera are as described above.

[0044] In particular, the antibody of the present invention preferably undergoes an antigen-antibody reaction with a ribosomal protein of any of the bacteria of the specific bacterial genus and / or selected bacterial genus described above. In particular, it is preferable that the antibody undergoes an antigen-antibody reaction with the ribosomal protein L7 / L12. In the present invention, "ribosomal protein L7 / L12" or simply "L7 / L12" is a type of ribosomal protein essential for protein synthesis in microorganisms, and is a protein commonly possessed by various bacteria. For the antibody that undergoes an antigen-antibody reaction with the ribosomal protein L7 / L12 of the above-mentioned bacteria and a method for producing the same, reference can be made to the description in, for example, International Publication No. WO 2000 / 006603, which is a patent publication related to a previous patent application filed by the present inventors.

[0045] The bacterial component that serves as an antigen for the antibody of the present invention is not limited. It may be a component contained in the cell wall or cell membrane exposed outside the bacterial cell, or a component contained in the cytoplasm, organelles, nucleus, etc. that is not exposed outside the bacterial cell. When the antibody of the present invention causes an antigen-antibody reaction with a component that is not exposed outside the bacterial cell, in order to cause an antigen-antibody reaction between the antibody of the present invention and such a bacterial component, the sample may be subjected to a treatment for lysing the bacteria before contacting the antibody of the present invention with a food, drink, environment, or biological sample. Such a lysis treatment will be described later.

[0046] The degree of the antigen-antibody reaction between the antibody of the present invention and the bacteria to be detected is not particularly limited, but it is sufficient that the antigen-antibody reaction occurs to an extent that can be detected by any known detection method. Methods for detecting the antigen-antibody reaction between the antibody and the bacteria include, but are not limited to, various known immunological measurement methods described below.

[0047] In addition, the antibody of the present invention preferably does not cross-react with one or more non-bacterial components that may be present in a sample. Examples of such non-bacterial components include, but are not limited to, various bioorganic compounds derived from viruses, plants, and / or animals that bacteria do not have. Specific examples of such bioorganic compounds include proteins, sugars, glycoproteins, lipids, complex lipids, nucleic acids, etc. It is preferable that the antibody of the present invention does not cross-react with at least one or more, usually three or more, even four or more, five or more, six or more, seven or more, eight or more, particularly nine or more, and particularly ten or more non-bacterial bioorganic compounds among these non-bacterial components.

[0048] Since antibodies have extremely high antigen specificity, they are effective for specifically capturing a specific antigen, but they have been considered unsuitable for detecting multiple different target substances. Furthermore, since the genera and types of bacteria to be detected during food and beverage testing are extremely diverse, it has been previously considered extremely difficult to simultaneously detect such multiple genera of bacteria through antigen-antibody reactions. However, as described in the Examples below, the present inventors have succeeded in obtaining antibodies that undergo antigen-antibody reactions with multiple genera of bacteria to be detected during testing of food and beverage samples or environmental samples, and can be used to simultaneously detect these bacteria. Such findings are extremely unexpected findings that contradict conventional technical common sense.

[0049] The structure of the antibody of the present invention is not particularly limited, but is preferably as follows: Note that antibodies defined only by the structural features described below are also included in the antibody of the present invention.

[0050] Specifically, the antibody of the present invention preferably has the following amino acid sequences as the amino acid sequences of each of the heavy chain and light chain variable regions.

[0051] The amino acid sequence of the heavy chain variable region (VH) preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5. Among these, it is particularly preferable that the VH sequence is any one of the amino acid sequences selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5.

[0052] The amino acid sequence of the light chain variable region (VL) preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6. Among these, the VL sequence is particularly preferably any one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6.

[0053] Among these, preferred combinations of amino acid sequences of a heavy chain variable region (VH) and a light chain variable region (VL) are not limited to any one of the following combinations: a heavy chain variable region (VH) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:1, SEQ ID NO:3, and SEQ ID NO:5, and a light chain variable region (VL) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:2, SEQ ID NO:4, and SEQ ID NO:6. Among these, any one of the following combinations is particularly preferred.

[0054] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:1, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:2.

[0055] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 3, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 4.

[0056] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90%; particularly at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:5, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90% or at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:6.

[0057] In the present invention, the "homology" of two amino acid sequences is the ratio at which identical or similar amino acid residues appear at corresponding positions when both amino acid sequences are aligned, and the "identity" of two amino acid sequences is the ratio at which identical amino acid residues appear at corresponding positions when both amino acid sequences are aligned. The "homology" and "identity" of two amino acid sequences can be determined, for example, using the BLAST (Basic Local Alignment Search Tool) program (Altschul et al., J. Mol. Biol., (1990), 215(3):403-10) or the like.

[0058] Methods for identifying the sequences of each CDR from the variable sequences of the heavy and light chains of an antibody include, for example, the Kabat method (Kabat et al., The Journal of Immunology, 1991, Vol. 147, No. 5, pp. 1709-1719) and the Chothia method (Al-Lazikani et al., Journal of Molecular Biology, 1997, Vol. 273, No. 4, pp. 927-948). These methods are common technical knowledge in this field, and reference can also be made to, for example, the website of Dr. Andrew CR Martin's Group (http: / / www.bioinf.org.uk / abs / ).

[0059] In addition, examples of amino acids similar to a certain amino acid include amino acids that belong to the same group in the following classification based on the polarity, charge, and size of amino acids (each type of amino acid is represented by a one-letter code in each case). Aromatic amino acids: F, H, W, Y; Aliphatic amino acids: I, L, V; Hydrophobic amino acids: A, C, F, H, I, K, L, M, T, V, W, Y; Charged amino acids: D, E, H, K, R etc.; · Positively charged amino acids: H, K, R; · Negatively charged amino acids: D, E; Polar amino acids: C, D, E, H, K, N, Q, R, S, T, W, Y; Small amino acids: A, C, D, G, N, P, S, T, V etc.; ·Very small amino acids: A, C, G, S.

[0060] Furthermore, amino acids similar to a certain amino acid include amino acids that belong to the same group in the following classification based on the type of amino acid side chain (each type of amino acid is represented by a one-letter code in each case). · Amino acids with aliphatic side chains: G, A, V, L, I; · Amino acids with aromatic side chains: F, Y, W; · Amino acids with sulfur-containing side chains: C, M; · Amino acids with aliphatic hydroxyl side chains: S, T; · Amino acids with basic side chains: K, R, H; · Acidic amino acids and their amide derivatives: D, E, N, Q.

[0061] The method for producing the antibody of the present invention is not particularly limited. When the antibody of the present invention is a polyclonal antibody, it can be produced using a component derived from the bacteria to be detected. Examples of the component derived from the bacteria that can be used include the bacterial cell itself, a lysate obtained by lysing the bacterial cell, and a fraction obtained by electrophoresis of the lysate. When a fraction obtained by electrophoresis of a bacterial lysate is used, the fraction to be used is not limited, but it is preferable to select and use a fraction corresponding to a molecular weight of about 10 to 20 kDa. In addition, it is preferable to use a ribosomal protein contained in the bacteria as the component derived from the bacteria, and it is particularly preferable to use ribosomal protein L7 / L12. These components derived from the bacteria are inoculated into an animal together with an adjuvant as necessary, and the serum is collected, whereby antiserum containing an antibody (polyclonal antibody) that causes an antigen-antibody reaction with the predetermined multiple types of bacteria can be obtained. The animal to be inoculated is a sheep, a horse, a goat, a rabbit, a mouse, a rat, etc., and sheep and rabbits are particularly preferable for producing polyclonal antibodies. In addition, the antibodies are purified and fractionated from the obtained antiserum, and the desired antibodies with superior specificity can be obtained by appropriately screening using known methods, using as indicators whether the antibodies react with the desired bacteria and whether they do not cross-react with other components derived from food and beverages, the environment, or living organisms. Furthermore, it is also possible to obtain monoclonal antibodies by isolating antibody-producing cells that produce the desired antibody molecules and fusing them with myeloma cells to produce hybridomas with autonomous proliferation ability. In addition, as a method that does not require sensitization of animals, a technology is also available in which an antibody that specifically binds to a component derived from the bacteria to be detected or a phage clone consisting of a specific amino acid sequence is obtained using a phage library that expresses the heavy chain variable (VH) region or light chain variable (VL) region of an antibody or a part of them, and an antibody is produced from the information.

[0062] Furthermore, if a desired antibody is obtained by the above procedure, the structure of the antibody, specifically, a part or all of the amino acid sequences of the heavy chain constant (CH) region, the heavy chain variable (VH) region, the light chain constant (CL) region, and / or the light chain variable (VL) region can be analyzed using a known amino acid sequence analysis method. A method for modifying the amino acid sequence of the desired antibody thus obtained to improve the binding ability and specificity of the antibody is also known to those skilled in the art. Furthermore, it is also possible to use the whole or part of the amino acid sequence of the desired antibody (particularly the whole or part of the heavy chain variable (VH) region and the light chain variable (VL) region, especially the amino acid sequence of each CDR) and combine it with a part of the amino acid sequence of a known antibody (particularly the heavy chain constant (CH) region and the light chain constant (CL) region, and optionally the amino acid sequence of each FR of the heavy chain variable (VH) region and the light chain variable (VL) region) as necessary, thereby designing another antibody that is highly likely to have the same antigen specificity.

[0063] Once the amino acid sequence of a desired antibody has been identified, a nucleic acid molecule having a base sequence encoding all or part of the amino acid sequence of the desired antibody can be prepared by known techniques, and the antibody can be prepared by genetic engineering using the nucleic acid molecule. Furthermore, a vector or plasmid for expressing each component of the desired antibody can be prepared from the base sequence and introduced into a host cell (mammalian cell, insect cell, plant cell, yeast cell, microbial cell, etc.) to produce the antibody. Furthermore, for the purpose of improving the performance of the obtained antibody or avoiding side effects, the structure of the constant region of the antibody or the sugar chain portion can be appropriately modified by techniques well known to those skilled in the art.

[0064] The present invention also covers the above-described methods for producing the antibodies of the present invention, the nucleic acid molecules encoding the antibodies of the present invention, vectors or plasmids containing such nucleic acid molecules, cells containing such nucleic acid molecules, vectors or plasmids, and hybridomas producing the antibodies of the present invention.

[0065] The techniques for producing and modifying antibodies described herein are all known to those skilled in the art, and may be found, for example, in Antibodies; A laboratory manual, E. Harlow et al., Cold Spring Harbor Laboratory Press (2014). The molecular biology techniques described herein (e.g., amino acid sequence analysis, nucleic acid molecule design and production methods, vector and plasmid design and production methods, etc.) are all known to those skilled in the art, and may be found, for example, in Molecular Cloning, A laboratory manual, Cold Spring Harbor Laboratory Press, Shambrook, J. et al. (1989).

[0066] In this way, the preferred embodiment of the method of the present invention is to use an antibody (the antibody of the present invention) that recognizes the ribosomal protein of each bacterium and causes an antigen-antibody reaction, and to contact the sample to detect the antigen-antibody reaction. Here, the detection sensitivity can be improved by exposing the ribosomal protein of the bacteria present in the sample to the outside of the bacterial cell membrane before contacting the antibody of the present invention with the sample. Therefore, in a preferred embodiment of the method of the present invention using the antibody of the present invention described below, the sample may be subjected to a treatment to lyse the bacteria before contacting the antibody of the present invention with the sample. Examples of such bacterial lysis treatment include, but are not limited to, heat treatment, ultrasonic treatment, chemical treatment with a surfactant, and the like. The conditions used for the lysis treatment can be appropriately determined depending on the type of bacteria contained in the sample. In addition, in a preferred embodiment of the method of the present invention using the antibody of the present invention, the method of contacting the antibody of the present invention with a food, drink, environment, or biological sample is also arbitrary.

[0067] In a preferred embodiment of the method of the present invention using the antibody of the present invention, the immunoassay for detecting the antigen-antibody reaction is not limited. Examples of the immunoassay are not limited, and may be a method using a single antibody or a method using two or more types of antibodies.

[0068] Examples of immunoassays using a single antibody include, but are not limited to, ELISA (enzyme-linked immunosorbent assay) which uses a microtiter plate carrying bacterial antigens to confirm the antigen-antibody reaction caused by the antibody; biosensors which carry an antibody (or antigen) on the sensor surface and confirm the antigen-antibody reaction with the antigen (or antibody) electrically (e.g., AC impedance assay, FET (field effect transistor) assay, etc.) or optically (e.g., SPR (surface plasmon resonance) assay, etc.), and various other known immunoassays can be used for any of these.

[0069] Examples of immunoassays using two or more types of antibodies include, but are not limited to, various known immunoassays, such as ELISA using a microtiter plate carrying an antibody, latex particle agglutination assay using latex particles carrying an antibody (e.g., polystyrene latex particles, etc.), immunochromatography using a membrane carrying an antibody, and a sandwich assay using a detection antibody labeled with colored particles or particles having color-developing ability, enzymes, fluorescent bodies, etc., and a capture antibody immobilized on a solid-phase carrier such as magnetic particles. In the case of an immunoassay using two or more types of antibodies, a detection antibody and a capture antibody, such as a sandwich assay, the antibody of the present invention may be used as either a capture antibody or a detection antibody.

[0070] [3. Method for detecting the presence and / or amount of bacteria in a specimen (2)] In particular, in the present invention, it is preferable to use a sandwich assay method in which the presence or absence and / or amount of bacteria in a specimen is detected by a process of capturing and labeling bacteria in the specimen through an antigen-antibody reaction between the specimen, a capture antibody linked to a solid phase carrier, and a detection antibody having a detection label, and a process of detecting the target bacteria in the specimen based on the detection label. Such a method (hereinafter appropriately abbreviated as "method (2) of the present invention") will be described below.

[0071] The method (2) of the present invention is a method comprising: (I) a step of capturing and labeling bacteria in a sample by an antigen-antibody reaction between the sample, a capture antibody linked to a solid-phase carrier, and a detection antibody having a detection label, and (II) a step of detecting the presence or absence and / or amount of bacteria in a sample by detecting the target bacteria in the sample based on the detection label. In this method, one of the capture antibody and the detection antibody is one or more specific antibodies that undergo an antigen-antibody reaction with one or more target bacteria, and the other antibody is one or more general-purpose antibodies that undergo an antigen-antibody reaction with five or more genera of bacteria including the target bacteria.

[0072] In one embodiment of the method (2) of the present invention (which will be appropriately referred to as "embodiment A"), the step (I) is (Ia-1) contacting a specimen with a detection antibody and labeling the bacteria in the specimen by an antigen-antibody reaction between the detection antibody and the bacteria; and (Ia-2) A step of contacting a specimen containing bacteria labeled with a detection antibody with a capture antibody and capturing the bacteria in the specimen by an antigen-antibody reaction between the capture antibody and the bacteria-detection antibody complex. may also include

[0073] In another embodiment of the method (2) of the present invention (which will be appropriately referred to as "embodiment B"), the step (I) is (Ib-1) contacting a specimen with a capture antibody and capturing bacteria in the specimen through an antigen-antibody reaction between the capture antibody and the bacteria; and (Ib-2) A step of contacting a specimen containing the bacteria captured by the capture antibody with a detection antibody, and labeling the bacteria in the specimen by an antigen-antibody reaction between the detection antibody and the bacteria-capture antibody complex. may also include

[0074] In any embodiment, the capture antibody may be a general-purpose antibody and the detection antibody may be a specific antibody, or the detection antibody may be a general-purpose antibody and the capture antibody may be a specific antibody. In addition, any of the general-purpose antibodies and specific antibodies may be the antibody of the present invention. Among them, according to one embodiment of the present invention, the antibody of the present invention is preferably used as a general-purpose antibody, although it is not limited thereto. In addition, unless otherwise specified, in this specification, a "specific antibody" means an antibody that causes an antigen-antibody reaction with one or more types of bacteria (detection target bacteria) that are the final detection target, and a "general-purpose antibody" means an antibody that causes an antigen-antibody reaction with bacteria of 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, or 10 or more, or 11 or more genera including the detection target bacteria.

[0075] In the method (2) of the present invention, the selection of either mode A or mode B may be made depending on the type of immunoassay and the type of specimen to be actually used. Examples of the immunoassay include, but are not limited to, various known immunoassays, such as ELISA (enzyme-linked immunosorbent assay) using a microtiter plate carrying an antibody, latex particle agglutination assay using latex particles (e.g., polystyrene latex particles, etc.) carrying an antibody, immunochromatography using a membrane carrying an antibody, and a sandwich assay using a detection antibody labeled with colored particles or particles having color-developing ability, an enzyme, a fluorescent substance, or the like, and a capture antibody immobilized on a solid-phase carrier such as magnetic particles.

[0076] Hereinafter, an example will be described in which the method (2) of the present invention according to aspect A is carried out using immunochromatography as the immunoassay method. However, when using other immunoassay methods, each feature can be appropriately modified.

[0077] In the step (Ia-1), that is, the step of contacting the specimen with the detection antibody and labeling the bacteria in the specimen by the antigen-antibody reaction between the detection antibody and the bacteria, the detection antibody having a detection label is contacted with the specimen, and the bacteria in the specimen are labeled by the antigen-antibody reaction between the detection antibody and the bacteria. The method of contacting the specimen with the detection antibody is not limited, but it is usually carried out by introducing a specimen prepared as an aqueous specimen into a member region impregnated with the detection antibody and maintaining it for a certain period of time. The specific embodiment differs depending on the capture embodiment of step (a), but as an example, a conjugate pad to which the detection antibody is attached is placed upstream of a solid phase carrier (porous membrane) to which the capture antibody is immobilized, and the specimen prepared as an aqueous specimen is introduced into the conjugate pad portion and allowed to permeate, thereby contacting the specimen with the detection antibody. As another example, when a flow path is used as the solid phase carrier, the specimen prepared as an aqueous specimen may be contacted with the detection antibody upstream of the position of the capture antibody immobilized on the flow path or before being introduced into the solid phase carrier.

[0078] In the step (Ia-2), that is, the step of contacting a specimen containing bacteria labeled with a detection antibody with a capture antibody and capturing bacteria in the specimen by an antigen-antibody reaction between the capture antibody and the bacteria-detection antibody complex, the capture antibody is brought into contact with the specimen, and the bacteria in the specimen are captured by an antigen-antibody reaction between the capture antibody and the bacteria. The method of contacting the specimen with the capture antibody is not limited, but it is usually carried out by introducing a specimen prepared as an aqueous specimen into an area where the capture antibody is present and maintaining it for a certain period of time. The specific embodiment varies depending on the type of solid phase carrier of the capture antibody, and the like. For example, a porous membrane is used as the solid phase carrier, and the bacteria-detection antibody complex is introduced and permeated through the porous membrane on which the capture antibody is immobilized, so that the capture antibody immobilized on the porous membrane captures the bacteria in the specimen. As another example, the capture antibody may be immobilized in one area on a flow path as a solid phase carrier, and the bacteria-detection antibody complex may be circulated through the flow path, so that the capture antibody immobilized in one area on the flow path captures the bacteria in the specimen.

[0079] In the step (II), i.e., the step of detecting the target bacteria in the specimen based on the detection label, the target bacteria captured by the capture antibody and labeled by the detection antibody are detected based on the detection label. The detection method is not particularly limited and may be appropriately selected depending on the type of detection label, but for example, when a metal colloid such as gold colloid is used as the detection label, the presence or absence or amount of gold colloid bound to the target bacteria may be detected by any method such as visual inspection or a camera.

[0080] According to the method (2) of the present invention described above, by appropriately combining a general-purpose antibody that undergoes a wide range of antigen-antibody reactions with many types of bacteria with a specific antibody that undergoes a specific antigen-antibody reaction only with a specific type of bacteria, it becomes possible to distinguish a desired bacterium from other bacteria and other components in a sample and detect it simply and efficiently. In particular, by using a plurality of specific antibodies in appropriate combination, it becomes possible to design a detection system that corresponds to various desired combinations of bacteria. In addition, the method (2) of the present invention can be carried out by utilizing any immunoassay method as long as it uses a capture antibody and a detection antibody.

[0081] Specifically, when an antibody of the present invention is used as the above-mentioned general antibody, an antibody of the present invention that undergoes an antigen-antibody reaction with a wide range of bacteria (usually five or more genera) including the bacteria to be ultimately detected (i.e., has relatively low specificity) is prepared as the general antibody, and an antibody that specifically undergoes an antigen-antibody reaction with the bacteria to be ultimately detected among the bacteria with which the general antibody undergoes an antigen-antibody reaction but does not undergo an antigen-antibody reaction with other bacteria is prepared as a specific antibody, and these can be used in combination.

[0082] As mentioned above, the general-purpose antibody may be used as a capture antibody or a detection antibody, but is preferably used as a detection antibody. The detection antibody needs to be labeled for detection, and the labeling conditions (pH, salt concentration, buffer type, etc.) need to be optimized according to the type of antibody used. By using the general-purpose antibody as a detection antibody, the same general-purpose antibody can be used even if the bacteria to be detected change, so there is no need to optimize the labeling conditions, which is advantageous in producing a kit for sandwich assays.

[0083] On the other hand, when the above-mentioned general-purpose antibody is used as the specific antibody, an antibody of the present invention that undergoes an antigen-antibody reaction with two or more genera of bacteria that are the final detection targets, but does not undergo an antigen-antibody reaction with bacteria of other genera (i.e., has a relatively high specificity) is prepared as the specific antibody, and an antibody that undergoes an antigen-antibody reaction with a wide range of bacteria genera other than the bacteria to be detected (with which the antibody of the present invention does not undergo an antigen-antibody reaction) is prepared as the general-purpose antibody, and these can be used in combination.

[0084] In the method (2) of the present invention, it is preferable that the specific antibody undergoes an antigen-antibody reaction only with bacteria of a limited genus. Specifically, the range of bacteria with which the specific antibody undergoes an antigen-antibody reaction is made to coincide with the range of bacteria to be detected. When only a single specific antibody is used, the range of bacteria with which the specific antibody undergoes an antigen-antibody reaction is made to coincide with the range of bacteria to be detected. On the other hand, when two or more specific antibodies are used in combination, the combined range of bacteria with which each of the specific antibodies undergoes an antigen-antibody reaction should coincide with the range of bacteria to be detected. In particular, according to the latter embodiment, by appropriately combining a plurality of specific antibodies each of which undergoes an antigen-antibody reaction with different bacteria, it is possible to adjust the range of bacteria to be detected in various ways, which is extremely advantageous.

[0085] In the method (2) of the present invention, each specific antibody may react with at least one genus of bacteria. The specific genus of bacteria with which each specific antibody reacts is not limited, but it is preferable that each specific antibody reacts with at least one or more genus of bacteria selected from the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

[0086] In method (2) of the present invention, it is preferable that each of the universal antibodies is an antibody that generates an antigen-antibody reaction with bacteria of at least 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, or 10 or more, or 11 or more genera selected from the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

[0087] In the method (2) of the present invention, the structures of the general antibody and the specific antibody are not particularly limited, but it is preferable that the amino acid sequences of the heavy chain and light chain variable regions thereof are as follows:

[0088] The amino acid sequence of the heavy chain variable region (VH) of the generic antibody preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5. Among these, it is particularly preferable that the VH sequence is any one of the amino acid sequences selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5.

[0089] The amino acid sequence of the light chain variable region (VL) of the generic antibody preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6. Among these, it is particularly preferable that the VL sequence is any one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 6.

[0090] Preferred combinations of amino acid sequences of a heavy chain variable region (VH) and a light chain variable region (VL) for a versatile antibody are not limited, and can be any combination of a heavy chain variable region (VH) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:1, SEQ ID NO:3, and SEQ ID NO:5, and a light chain variable region (VL) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:2, SEQ ID NO:4, and SEQ ID NO:6. Among these, any of the following combinations is particularly preferred.

[0091] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:1, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:2.

[0092] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 3, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 4.

[0093] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90%; particularly at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:5, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90% or at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO:6.

[0094] On the other hand, the amino acid sequence of the heavy chain variable region (VH) of the specific antibody preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, and SEQ ID NO:13. Among them, it is particularly preferable that the VH sequence is identical to any one of the amino acid sequences selected from SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, and SEQ ID NO:13.

[0095] The amino acid sequence of the light chain variable region (VL) of the specific antibody preferably has an amino acid sequence having 80% or more, particularly 85% or more, further 90% or more, particularly 95% or more, or 96% or more, or 97% or more, or 98% or more, or 99% or more, and particularly 100% homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, and SEQ ID NO:14. Among them, it is particularly preferable that the VL sequence is identical to any one of the amino acid sequences selected from SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, and SEQ ID NO:14.

[0096] Preferred combinations of amino acid sequences of the heavy chain variable region (VH) and light chain variable region (VL) for a specific antibody are not limited, and can include any combination of a heavy chain variable region (VH) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:11, and SEQ ID NO:13, and a light chain variable region (VL) having an amino acid sequence that has 80% or more homology (preferably identity) with any one of the amino acid sequences selected from SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:12, and SEQ ID NO:14. Among these, any of the following combinations is particularly preferred.

[0097] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90%; particularly at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 7, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90% or at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 8.

[0098] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 9, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 10.

[0099] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90%; particularly at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 11, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85% or even at least 90% or at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 12.

[0100] a heavy chain variable region (VH) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 13, and a light chain variable region (VL) having an amino acid sequence which has at least 80% homology (preferably at least 85%; even more preferably at least 90%; particularly preferably at least 95% or at least 96% or at least 97% or at least 98% or at least 99% and in particular 100% identity) with the amino acid sequence of SEQ ID NO: 14.

[0101] [4. Kit for detecting the presence and / or amount of bacteria in a specimen] The present invention also encompasses a kit (kit of the present invention) that contains the above-described antibody of the present invention for use in the above-described method of the present invention.

[0102] The kit of the present invention includes, in addition to the antibody of the present invention, one or more reagents necessary for carrying out the method of the present invention using the antibody of the present invention, a detection device or its components, and / or instructions describing the procedure for carrying out the method of the present invention. The types of such reagents, the contents of the instructions, and further other components included in the kit of the present invention may be appropriately determined depending on the type of specific immunological assay used to detect bacteria of multiple genera.

[0103] When the kit of the present invention includes a detection device or its components, the device constituted by such a kit is a device equipped with components necessary for carrying out the method of the present invention using the antibody of the present invention (hereinafter, appropriately abbreviated as "the device of the present invention"). The specific components of the device of the present invention can be appropriately adjusted according to the type of immunoassay, which is a specific embodiment of the method of the present invention. As described above, examples of immunoassays include, but are not limited to, ELISA (enzyme-linked immunosorbent assay) using a microtiter plate carrying an antibody; latex particle agglutination assay using latex particles (e.g., polystyrene latex particles, etc.) carrying an antibody; immunochromatography using a membrane carrying an antibody; a sandwich assay using a detection antibody labeled with colored particles or particles having color-developing ability, enzymes, or fluorescent bodies, etc., and a capture antibody immobilized on a solid phase carrier such as magnetic particles, an ELISA method using one antibody, a biosensor method, and various other known immunoassays. The device of the present invention is equipped with components necessary for carrying out such various immunoassays.

[0104] Specific examples of devices capable of simultaneously and easily detecting the presence or absence and / or abundance of multiple genera of bacteria in a specimen include a lateral flow type device and a flow-through type device. Here, the lateral flow type is a method in which a target specimen and a detection antibody are developed in parallel to a membrane including a detection region having a capture antibody immobilized on its surface, and a target substance captured in the detection region of the membrane is detected. On the other hand, the flow-through type is a method in which a target specimen and a detection antibody are passed vertically through a membrane having a capture antibody immobilized on its surface, and a target substance captured on the surface of the membrane is detected. The method of the present invention can be applied to both a lateral flow type device and a flow-through type device.

[0105] Both lateral flow type devices and flow-through type immunochromatographic detection devices are publicly known, and procedures other than those described in this disclosure can be appropriately designed by a person skilled in the art based on common technical knowledge. Below, the schematic configuration of the detection mechanism of the lateral flow type immunochromatographic detection device will be described with reference to the drawings, but this is merely one example of the schematic configuration of the detection procedure, and the configuration of the lateral flow type immunochromatographic detection device is not limited to the embodiment exemplified in the drawings.

[0106] FIG. 1 is a cross-sectional view showing a schematic configuration of a strip-shaped detection mechanism, which is an example of the detection mechanism of a lateral flow type immunochromatographic detection device. In the detection mechanism 10 of FIG. 1, a strip-shaped detection antibody-impregnated member (conjugate pad) 2 (this pad is impregnated with a detection antibody) and a specimen addition member (sample pad) 3 are arranged on one end side (upstream side of specimen flow B) of a strip length direction on an insoluble membrane carrier 1 for chromatographic development, and an absorption member (absorption pad) 4 is arranged on the other end side (downstream side of specimen flow B). In the center of the strip length direction on the insoluble membrane carrier 1, a site 5 where a capture antibody is immobilized and a site 6 where a control reagent is immobilized as necessary are arranged. The control reagent is a reagent that does not bind to the analyte but binds to the detection antibody. When a specimen A is applied onto the specimen addition member (sample pad) 3, the specimen A passes through the detection antibody-impregnated member (conjugate pad) 2 and flows through the insoluble membrane carrier 1 in the direction of the specimen flow A. At this time, the analyte in the specimen (bacteria to be detected in the present invention) binds to the detection antibody to form an analyte-detection antibody complex. When specimen A passes through the capture antibody fixing site 5, the analyte in the specimen binds to the capture antibody to form a capture antibody-analyte-detection antibody complex. Furthermore, when specimen A passes through the control reagent fixing site 6, the detection antibody that is not bound to the analyte binds to the control reagent 6, thereby confirming the end of the test (i.e., specimen A has passed through the capture antibody 5). Here, the presence or absence or amount of the analyte can be detected by detecting the label possessed by the detection antibody in the capture antibody-analyte-detection antibody complex present at the capture antibody fixing site 5 by a known means. If necessary, the label of the detection antibody may be sensitized by a known method to facilitate detection.

[0107] The type of solid phase carrier used for the capture antibody is not particularly limited, but specific examples include porous membranes made of cellulose, nitrocellulose, cellulose acetate, nylon, PVDF (Polyvinylidene Difluoride), glass fiber, etc.; flow channels made of glass, plastic, PDMS (Poly(dimethylsiloxane)), silicon, etc.; thread, paper, fiber, etc. The method for linking an antibody to a solid phase carrier is not particularly limited, and specific examples include immobilization by physical adsorption utilizing the hydrophobicity of the antibody, and immobilization by chemical bonding utilizing the functional groups of the antibody.

[0108] The type of detection label used for the detection antibody is not particularly limited and may be selected appropriately depending on the detection method. Specific examples of the detection label include metal colloids such as gold colloid, platinum colloid, palladium colloid, etc.; non-metallic colloids such as selenium colloid, alumina colloid, silica colloid, etc.; insoluble granular substances such as colored resin particles, dye colloids, colored liposomes, etc.; color-developing reaction catalytic enzymes such as alkaline phosphatase, peroxidase, luciferase, etc.; fluorescent dyes, radioactive isotopes; chemiluminescent labels, bioluminescent labels, electrochemiluminescent labels, etc.

[0109] The method for labeling the antibody is not particularly limited, and specific examples include physical adsorption utilizing the hydrophobicity of the antibody and chemical bonding utilizing the functional groups of the antibody.

[0110] The detection antibody-impregnated member (conjugate pad) 2 and the specimen addition member (sample pad) 3 can be omitted as desired. If the detection antibody-impregnated member (conjugate pad) 2 is not provided in this system, the specimen A and the detection antibody can be simultaneously or sequentially applied to one end of the insoluble membrane carrier 1 in a premixed state or separately, to perform a test similar to the above test.

[0111] In addition, even if the capture antibody and the detection antibody are interchanged, a detection kit capable of similar detection can be constructed. That is, the capture antibody may be a general-purpose antibody and the detection antibody may be a specific antibody, or the detection antibody may be a general-purpose antibody and the capture antibody may be a specific antibody. As described above, either or both of the general-purpose antibody and the specific antibody may be the antibody of the present invention.

[0112] Among them, it is more preferable to use a general-purpose antibody as the detection antibody as described above. For example, when gold colloid is used as a detection label, it is necessary to perform excessive optimization of the labeling conditions (pH, salt concentration, blocking agent, type of buffer solution, type of dispersion liquid, centrifugation conditions, etc.) depending on the type of antibody used. On the other hand, since the capture antibody is simply applied to an insoluble membrane carrier and dried, excessive optimization of conditions depending on the type of antibody is not required. Since the general-purpose antibody of the present invention undergoes a wide antigen-antibody reaction regardless of the type of bacteria, the same general-purpose antibody (detection antibody) can be used even if the bacteria to be detected are changed, there is no need to perform such excessive optimization of the labeling conditions, which is extremely advantageous in producing an immunochromatography kit.

[0113] In the above-described lateral flow immunochromatographic detection method and device according to one embodiment of the present invention, it is possible to simultaneously detect two or more genera of bacteria to be detected in a single detection line (the capture antibody immobilization site 5 in the example of FIG. 1). In the conventional lateral flow immunochromatographic detection method and device, when detecting multiple detection targets, a detection line (the capture antibody immobilization site 5 in the example of FIG. 1) must be provided for each detection target, and thus it is necessary to provide detection lines corresponding to the number of detection targets. This leads to an increase in the size of the device, and in addition, when the number of detection targets is too large, it is difficult or impossible to detect them with a single device in the first place. In contrast, in the lateral flow immunochromatographic detection method and device according to one embodiment of the present invention, it is possible to simultaneously detect multiple genera of detection target bacteria with a single detection line by appropriately combining detection antibodies and capture antibodies. This allows the device to be miniaturized, and even if the number of species and genera of detection target bacteria is large, detection is possible in principle with a single device, and the total amount of detection target bacteria can be determined with a single detection line.

[0114] The present invention also provides a method for producing the above-mentioned immunochromatography kit, the method including at least the steps of: laminating the conjugate pad, to which the detection antibody is attached, on the insoluble membrane carrier; and immobilizing the capture antibody in the chromatographic development direction relative to the conjugate pad on the insoluble membrane carrier.

[0115] Here, of the capture antibody and the detection antibody, either one may be the specific antibody and the other may be the general-purpose antibody, but it is preferable to use the specific antibody as the capture antibody and the general-purpose antibody as the detection antibody.

[0116] Here, the specific antibody is preferably an antibody that specifically induces an antigen-antibody reaction with the target bacteria of at least one genera selected from the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

[0117] In addition, it is preferable that the general-purpose antibody specifically reacts with five or more genera of target bacteria selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

[0118] According to the above-described manufacturing method of the immunochromatography kit of the present invention, when manufacturing / mass-producing immunochromatography kits of multiple variations, it is possible to commonly use the same general-purpose antibody as the detection antibody, which is extremely effective in that multiple types of immunochromatography kits can be manufactured by simply selecting the capture antibody. EXAMPLES

[0119] The present invention will be described in more detail below with reference to examples. However, the present invention is not limited to the following examples, and can be carried out in any form without departing from the spirit of the present invention.

[0120] [1. Preparation of antibodies] · Preparation of universal antibody A (PA51B2) Pseudomonas aeruginosa (PA) was used as the bacterium immunogen. Antibodies against ribosomal protein L7 / L12 of Pseudomonas aeruginosa were produced with reference to the method described in International Publication No. 2000 / 06603. Specifically, Escherichia coli transformed with an expression vector incorporating DNA encoding the entire amino acid sequence of ribosomal protein L7 / L12 of Pseudomonas aeruginosa was cultured in LB medium or the like, and purified as a fusion protein using a tag sequence derived from the expression vector by affinity column. This Pseudomonas aeruginosa L7 / L12 full-length protein was used as an immunogen, and according to the standard method for obtaining hybridomas, the immunogen was prepared in PBS so that the concentration of the immunogen was 0.4 mg / mL, and the same amount of Freund's adjuvant was added, and mice were immunized four times so that the immunogen amount was 50 μg / time. After confirming the increase in serum antibody titer by test blood collection, spleen cells of the mice were extracted. The extracted mouse spleen cells were fused with myeloma cells to obtain various hybridomas.

[0121] The obtained hybridomas were cultured in HAT medium and screened using antibodies in the culture supernatant. Screening was performed by ELISA using bacterial lysates of multiple genera immobilized as antigens, and hybridomas producing antibodies that reacted simultaneously with lysates of 11 bacterial species, namely, Escherichia coli (EC), Staphylococcus aureus (SA), Pseudomonas aeruginosa (PA), Bacillus subtilis (BS), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Listeria monocytogenes (LM), Enterobacter cloacae (ECL), and Salmonella enterica (SE), were selected. Following the standard method for monoclonal antibody production, the selected hybridomas were cultured in TIL Media I medium supplemented with 10% fetal bovine serum (FBS), and administered intraperitoneally to mice, and ascites was collected. The collected ascites was centrifuged to separate floating matter and red blood cells, and then filtered through a filter with a mesh size of 0.45 μm. The filtrate was passed through a Protein G column to adsorb the antibody, thereby purifying and obtaining generic antibody A (PA51B2) corresponding to the antibody of the present invention from the mouse ascites.

[0122] ·Generic antibody B (LP54A3) Generic antibody B (LP54A3), which corresponds to the antibody of the present invention, was produced using a procedure similar to that for obtaining generic antibody A, except that Legionella pneumophila (LP) was used as the immunogen bacterium and Legionella pneumophila ribosomal protein L7 / L12 was used as the immunogen.

[0123] · Generation of universal antibody C (CP141A190.1) Generic antibody C (CP141A190.1), which corresponds to the antibody of the present invention, was produced using a procedure similar to that for obtaining generic antibody A, except that Chlamydia trachomatis (CP) was used as the immunogen bacterium and Chlamydia trachomatis ribosomal protein L7 / L12 was used as the immunogen.

[0124] - Preparation of specific antibody A (HI142D11.3) Haemophilus influenzae (HI) was used as the bacterium immunogen. Antibodies against ribosomal protein L7 / L12 of Haemophilus influenzae were produced with reference to the method described in International Publication WO 2000 / 06603. Specifically, Escherichia coli transformed with an expression vector incorporating DNA encoding the entire amino acid sequence of ribosomal protein L7 / L12 of Haemophilus influenzae was cultured in LB medium or the like, and purified as a fusion protein using a tag sequence derived from the expression vector by affinity column. This full-length Haemophilus influenzae L7 / L12 protein was used as an immunogen, and according to the standard method for obtaining hybridomas, the immunogen was prepared in PBS so that the concentration of the immunogen was 0.4 mg / mL, and the same amount of Freund's adjuvant was added, and mice were immunized four times so that the immunogen amount was 50 μg / time. After confirming the increase in serum antibody titer by test blood collection, spleen cells of the mice were extracted. The extracted mouse spleen cells were fused with myeloma cells to obtain various hybridomas.

[0125] The obtained hybridomas were cultured in HAT medium, and screening was performed using the antibodies in the culture supernatant. Screening was performed by the ELISA method described above, and hybridomas producing antibodies that reacted simultaneously with bacterial lysates of nine bacterial species (Escherichia coli (EC), Pseudomonas aeruginosa (PA), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Listeria monocytogenes (LM), Enterobacter cloacae (ECL), and Salmonella enterica (SE)) were selected. According to the standard method for monoclonal antibody production, the selected hybridomas were cultured in TIL Media I medium supplemented with 10% fetal bovine serum (FBS), and administered intraperitoneally to mice, and ascites was collected. The collected ascites was centrifuged to separate floating matter and red blood cells, and then filtered through a filter with a mesh size of 0.45 μm. The obtained filtrate was passed through a Protein G column to adsorb the antibody, and the specific antibody A (HI142D11.3) was purified from the mouse ascites.

[0126] - Preparation of specific antibody B (SA75B2) Similarly, various hybridomas were obtained using Staphylococcus aureus (SA) as the immunogen bacterium in the same manner as above, and hybridomas producing antibodies reactive with bacterial lysates of two bacterial species (Staphylococcus aureus (SA) and Bacillus subtilis (BS)) were selected. Specific antibody B (SA75B2) was then produced in the same manner as above.

[0127] - Preparation of specific antibody C (PA78A2) Except for using Pseudomonas aeruginosa (PA) as the immunogen and using the ribosomal protein L7 / L12 of Pseudomonas aeruginosa as the immunogen, various hybridomas were obtained using the same procedure as that for obtaining general antibody A, and then hybridomas producing antibodies that reacted with bacterial lysates of Pseudomonas aeruginosa (PA) 1 species were selected. Specific antibody C (PA78A2) was then produced using the same procedure as above.

[0128] - Preparation of specific antibody D (EC50C1) Similarly, various hybridomas were obtained by the same procedure as that for obtaining universal antibody A, except that Escherichia coli (EC) was used as the immunogen and E. coli ribosomal protein L7 / L12 was used as the immunogen. Hybridomas producing antibodies reactive with bacterial lysates of seven species, namely, E. coli (EC), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Enterobacter cloacae (ECL), and Salmonella enterica (SE), were then selected. Specific antibody D (EC50C1) was then produced by the same procedure as above.

[0129] Determination of the amino acid sequences of the heavy and light chain variable sequences of the general antibodies A to C and the specific antibodies A to D For the generic antibodies A to C (antibodies of the present invention) and the specific antibodies A to D prepared by the above procedures, examples of the amino acid sequences of the heavy and light chain variable sequences were determined according to standard methods. The correspondence between each amino acid sequence and each SEQ ID NO: is shown below.

[0130] · Universal antibody A (PA51B2): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:1) Light chain variable sequence: amino acid sequence (SEQ ID NO:2) · Universal antibody B (LP54A3): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:3) Light chain variable sequence: amino acid sequence (SEQ ID NO:4) · Universal antibody C (CP141A190.1): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:5) Light chain variable sequence: amino acid sequence (SEQ ID NO:6) ·Specific antibody A (HI142D11.3): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:7) Light chain variable sequence: amino acid sequence (SEQ ID NO:8) ·Specific antibody B (SA75B2): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:9) Light chain variable sequence: amino acid sequence (SEQ ID NO: 10) ·Specific antibody C (PA78A2): Heavy chain variable sequence: amino acid sequence (SEQ ID NO:11) Light chain variable sequence: amino acid sequence (SEQ ID NO: 12) ·Specific antibody D (EC50C1): Heavy chain variable sequence: amino acid sequence (SEQ ID NO: 13) Light chain variable sequence: amino acid sequence (SEQ ID NO: 14)

[0131] [2. Detection of antigen-antibody reaction between antibodies and bacteria 1 / Bacteriolytic antigen solid-phase ELISA] Using the general antibodies A to C (the antibodies of the present invention) and the specific antibodies A to D prepared by the above procedure, data on reactivity with bacteria of multiple genera were obtained by ELISA. As bacteria of multiple genera, 11 species were selected, which are frequently detected in food and drink or environmental samples: Escherichia coli (EC), Staphylococcus aureus (SA), Pseudomonas aeruginosa (PA), Bacillus subtilis (BS), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Listeria monocytogenes (LM), Enterobacter cloacae (ECL), and Salmonella enterica (SE). Each of the above bacteria was purchased from ATCC and cultured, and 1 × e 8Each cfu / mL was prepared and suspended in PBS. Bacterial lysates were obtained for each bacterium by sonication and filtration through a 0.45 μm filter to remove debris.

[0132] 50μL of the bacterial lysate was dropped into each well of a 96-well polystyrene plate for ELISA and immobilized on the bottom of the plate. Each well was washed three times with PBS-T (PBS containing Tween 20), and then blocked with PBS containing 1% BSA (Bovine Serum Albumin). After blocking, each well was washed three times with PBS-T, and 50μL of 10μg / mL of general antibodies A to C and specific antibodies A and B were dropped into each well, and an antigen-antibody reaction was carried out for 1 hour. After the reaction, the wells were washed three times with PBS-T, and 50μL of secondary antibodies (Goat Anti-mouse IgG) labeled with 0.5μg / mL of HRP (Horse Radish Peroxidase), an enzyme for detection, were dropped into each well and the reaction was carried out. After the reaction, the wells were washed five times with PBS-T, and 100 μL of a mixture of TMB (Tetramethylbenzidine) and hydrogen peroxide, which is a color-developing substrate, was dropped into each well to carry out a color reaction. After 10 minutes, hydrochloric acid, which is a reaction stop solution, was dropped into each well, and the absorbance at 450 nm of each well was measured using a plate reader.

[0133] The measurement results are shown in Table 1 below. The results shown in this table indicate that the generic antibodies A to C react with higher sensitivity (absorbance was 0.3 or higher for each bacterium, and 1.0 or higher in most cases) with each of the bacterial samples compared to samples without bacteria. In other words, it was confirmed that the generic antibodies A to C obtained by immunization with different bacteria can each cause an antigen-antibody reaction with (detect) each of the bacterial samples. On the other hand, the specific antibodies A to D showed antigen-antibody reactivity only with specific bacteria.

[0134] [Table 1]

[0135] [3. Detection of antigen-antibody reaction between antibodies and bacteria 2 / Recombinant antigen solid-phase ELISA] Using the general antibodies A to C (the antibodies of the present invention) and the specific antibodies A to D prepared by the above procedure, data on reactivity with ribosomal proteins L7 / L12 of bacteria from multiple genera were obtained by ELISA. As bacteria from multiple genera, 11 species were selected, which are frequently detected in food and drink or environmental samples: Escherichia coli (EC), Staphylococcus aureus (SA), Pseudomonas aeruginosa (PA), Bacillus subtilis (BS), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Listeria monocytogenes (LM), Enterobacter cloacae (ECL), and Salmonella enterica (SE). Escherichia coli transformed with an expression vector incorporating DNA encoding the amino acid sequence of ribosomal protein L7 / L12 of each bacterial species was cultured in LB medium or the like, and the ribosomal protein L7 / L12 of each bacterial species was obtained by purifying it as a fusion protein using the tag sequence derived from the expression vector using an affinity column.

[0136] 50μL of ribosomal protein L7 / L12 of each bacterial species was dropped into each well of a 96-well polystyrene plate for ELISA and immobilized on the bottom surface. After washing each well three times with PBS-T (PBS containing Tween 20), blocking treatment was performed with PBS containing 1% BSA (Bovine Serum Albumin). After blocking and washing three times with PBS-T, 50μL of either of the general antibodies A to C and the specific antibodies A to D at 10μg / mL was dropped into each well and an antigen-antibody reaction was performed for 1 hour. After the reaction, the wells were washed three times with PBS-T, and 50μL of secondary antibody (Goat Anti-mouse IgG) labeled with 0.5μg / mL of HRP (Horse Radish Peroxidase), an enzyme for detection, was dropped into each well and the reaction was performed. After the reaction, the wells were washed five times with PBS-T, and 100 μL of a mixture of TMB (Tetramethylbenzidine) and hydrogen peroxide, which is a color-developing substrate, was dropped into each well to carry out a color reaction. After 10 minutes, hydrochloric acid, which is a reaction stop solution, was dropped into each well, and the absorbance at 450 nm of each well was measured using a plate reader.

[0137] The measurement results are shown in Table 2 below. This table shows that the generic antibodies A to C react with higher sensitivity (absorbance was 0.3 or higher for all bacteria, and 1.0 or higher in most cases) with each of the bacterial samples compared to samples without bacteria. In other words, it was confirmed that all of the generic antibodies A to C obtained by immunization with different bacteria can cause an antigen-antibody reaction with (can detect) the ribosomal protein L7 / L12 in each of the bacterial samples. On the other hand, the specific antibodies A to D showed antigen-antibody reactivity only with specific bacteria.

[0138] [Table 2]

[0139] [4. Verification of cross-reactivity of antibodies with non-bacterial components in food, beverage, and environmental samples / Solid-phase ELISA] Using the general antibodies A to C (the antibodies of the present invention) and the specific antibodies A to D prepared by the above procedure, data on the reactivity with non-bacterial components (food, drink, and environmental components) in various food, drink, and environmental samples were obtained by ELISA. As food samples, raw fish (yakisoba, horse mackerel), raw noodles (fried noodles), raw eggs, side dishes (potato salad), vegetables (cucumber (fruit vegetable), carrot (root vegetable), and lettuce (leaf vegetable)), and fresh and processed meat (beef rib, beef shoulder, pork loin, chicken breast, and ham) were purchased from a supermarket and used. 25 g of each of these ingredients was weighed and placed in a commercially available stomacher bag, and 225 ml of PBS was added to perform stomacher processing. A part of the stomacher processing solution was used with a filter with a mesh size of 0.45 μm to remove solid matter containing bacteria, to prepare a food sample free of bacteria for ELISA. As beverage samples, milk and tea were purchased from a supermarket and used. These beverages were each suspended in PBS at a concentration of 1 / 10, and solid matter containing bacteria was removed using a 0.45 μm filter to prepare bacteria-free beverage samples for ELISA. Environmental samples were prepared by wiping the surfaces of hands, cutting boards, knives, and refrigerator handles using a commercially available wiping kit (ELMEX Pro·mediaST-25, PBS), suspending them in the PBS provided with the kit, and then removing solid matter containing bacteria using a 0.45 μm filter to prepare bacteria-free environmental samples for ELISA.

[0140] 50μL of the above food and drink samples and environmental samples were dropped into each well of a 96-well polystyrene plate for ELISA and immobilized on the bottom of the plate. Each well was washed three times with PBS-T, and then blocked with PBS containing 1% BSA. After blocking, 50μL of 10μg / mL of general antibodies A to C and specific antibodies A to D were dropped into each well and reacted for 1 hour. After the reaction, the wells were washed three times with PBS-T, and 50μL of 0.5μg / mL of secondary antibodies (Goat Anti-mouse IgG) labeled with HRP, an enzyme for detection, were dropped and reacted. After the reaction, the wells were washed five times with PBS-T, and 100μL of a mixture of TMB and hydrogen peroxide, a color-developing substrate, was dropped into each well to perform a color-developing reaction. After 10 minutes, hydrochloric acid, a reaction stopping solution, was added dropwise to each well, and the absorbance at 450 nm of each well was measured using a plate reader.

[0141] The measurement results are shown in Table 3 below. The results shown in this table indicate that the generic antibodies A to C do not react with any of the components in the food, drink, and environmental samples that do not contain the above bacteria (all absorbances are less than 0.3). Combined with the results of the above-mentioned Examples, it was confirmed that the generic antibodies A to C do not react with any of the non-bacterial components (food, drink, and environmental components) in the above-mentioned food, drink, and environmental samples, but react only with the specific multiple genera of bacteria to be detected, that is, the presence or absence and / or amount of the specific multiple genera of bacteria to be detected in the food, drink, and environmental samples can be detected with high selectivity. In addition, the specific antibodies A to D did not show cross-reactivity with any of the non-bacterial components in the food, drink, and environmental samples.

[0142] [Table 3]

[0143] [5. Preparation of immunochromatographic detection kit] Preparation of immunochromatographic detection kit: Three types of immunochromatographic detection kits (a) to (c) were prepared using the above-mentioned general antibody A corresponding to the antibody of the present invention as a secondary antibody (detection antibody) and the above-mentioned specific antibodies A to D as primary antibodies (capture antibodies) in the combinations shown in (a) to (c) in Table 4 below. In addition, detection kits capable of similar detection were prepared by switching the types of antibodies used as the primary and secondary antibodies and using them in the combinations shown in (d) to (f) in Table 4 below. In particular, by using the common general antibody A as a detection antibody, it was possible to easily construct various detection kits without the need for excessive optimization of the labeling conditions for each antibody.

[0144] [Table 4]

[0145] Preparation of membrane carrier for immunochromatography: A solution containing 1.5 mg / mL of primary antibody ((a) specific antibody C, (b) specific antibody D, (c) a mixture of specific antibodies A and B) and 3% (v / v) trehalose was prepared in 10 mM sodium phosphate buffer solution. The obtained solution was applied to a commercially available nitrocellulose membrane cut to a width of 2.5 cm and a length of 15 cm, with 1 cm of the solution being applied. 2 The solution was applied in an amount of 1 μL per well and dried to prepare a membrane carrier for immunochromatographic development.

[0146] Preparation of antibodies for detecting colloidal gold labels and antibody-impregnated members for detecting colloidal gold labels: A commercially available colloidal gold solution (particle size 60 nm) was added to the tube, and then 100 mM potassium phosphate buffer (pH 6.5) was added and mixed. A secondary antibody (general purpose antibody A) was added in an amount of 1 / 10 to the tube and mixed to prepare a solution with an antibody concentration of 0.1 mg / mL. The solution was left to stand at room temperature for 30 minutes to bind the antibody to the surface of the colloidal gold particles. Then, a casein solution was added so that the final concentration in the colloidal gold solution was 0.1%, mixed, and left to stand for 60 minutes to perform a blocking treatment. The solution was centrifuged at 8000 g for 20 minutes, and the supernatant was removed with a pipette. A colloidal gold dispersion (0.25% casein, 40 mM NaCl, 5% sucrose, 10 mM Tris-HCl (pH 8.2)) was added to the tube, mixed, and redispersed to prepare a colloidal gold label detection antibody solution. A commercially available glass fiber sheet was impregnated with this detection antibody solution and then dried to obtain a gold colloid-labeled detection antibody-impregnated member.

[0147] Assembling the immunochromatographic detection kit: In addition to the immunochromatographic development membrane carrier and the antibody-impregnated member for detecting colloidal gold label prepared by the above procedure, cotton cloth was prepared as a member for adding specimens, and filter paper was prepared as an absorption member. These members were then attached to a commercially available polyethylene substrate, which was then cut to a width of 5 mm to prepare an immunochromatographic detection kit with a detection mechanism similar to that shown in Figure 1.

[0148] [6. Detection of bacteria using immunochromatography detection kits] Using each of the immunochromatographic detection kits (a) to (c) prepared above, detection of bacteria from multiple genera was performed. The 11 species of bacteria used were Escherichia coli (EC), Staphylococcus aureus (SA), Pseudomonas aeruginosa (PA), Bacillus subtilis (BS), Klebsiella pneumoniae (KP), Serratia liquefaciens (SL), Rahnella aquatilis (RA), Citrobacter freundii (CF), Listeria monocytogenes (LM), Enterobacter cloacae (ECL), and Salmonella enterica (SE), which are frequently detected in food, beverage, and environmental samples. Each of the 11 species was diluted with 1×e 8Each cfu / mL was prepared and suspended in PBS. Each bacterium was lysed by ultrasonication to obtain bacterial lysates of 11 species (bacterial samples for immunochromatographic assay). In addition, a PBS solution without bacterial lysates was prepared as a bacteria-free sample. Tween 20 was added to each of these samples to a final concentration of 1% for immunochromatographic development to prepare samples for immunochromatography.

[0149] The prepared samples (a sample without bacteria and a sample of 11 types of bacterial lysate) were added to the sample addition member area of ​​the above-mentioned immunochromatography detection kit, and after 30 minutes, the colored line at the application site of the capture antibody on the membrane carrier was visually confirmed.

[0150] The prepared samples (bacteria-free sample and sample of 11 types of bacteria lysate) were added to the specimen addition member area of ​​the immunochromatography detection kit under the above-mentioned conditions (a) to (c), and 30 minutes later, the line color development at the site of the membrane carrier where the capture antibody was applied was visually confirmed. The results are shown in Table 5 below. According to the results in this table, as intended, detection kit (a) detected only one species of bacteria, Pseudomonas aeruginosa (PA), detection kit (b) detected seven species of bacteria belonging to the Enterobacteriaceae family, and detection kit (c) detected all 11 species of bacteria (all bacteria). In other words, it was shown that by combining specific antibodies (the above-mentioned specific antibody A (PA78A2), specific antibody B (EC50C1), specific antibody C (HI142D11.3), and specific antibody D (SA75B2)) that undergo antigen-antibody reactions only with limited genera of bacteria with a general antibody (the above-mentioned general antibody A (PA51B2)) that undergoes antigen-antibody reactions broadly with many genera of bacteria, and preparing an immunochromatographic detection kit according to the purpose, the target bacteria can be detected easily and quickly.

[0151] As mentioned above, even if the target bacterial species changes, a common general-purpose antibody (more preferably used as a detection antibody) can be used, and by combining it with a specific antibody (more preferably used as a capture antibody) corresponding to the target bacterial species, an immunochromatography kit capable of detecting the target bacterial species can be manufactured without excessive consideration of conditions. Similar results were obtained with the detection kit using the combinations (d) to (f) in Table 4 above.

[0152] [Table 5]

[0153] [7. Verification of cross-reactivity of antibodies with food, beverage, and environmental components using immunochromatographic detection kits] Using the immunochromatography detection kits (a) to (c) prepared above, data on reactivity with non-bacterial components (food, drink, and environmental components) in various food, drink, and environmental samples were obtained. As food samples, raw fish (yakisoba, horse mackerel), raw noodles (fried noodles), raw eggs, side dishes (potato salad), vegetables (cucumber (fruit vegetable), carrot (root vegetable), and lettuce (leaf vegetable)), and meat and processed meat (beef rib, beef shoulder, pork loin, chicken breast, and ham) were purchased from a supermarket. 25 g of each of these ingredients was weighed and placed in a commercially available stomacher bag, and 225 ml of PBS was added to perform stomacher processing. A portion of the stomacher processing solution was used to remove solid matter including bacteria using a filter with a mesh size of 0.45 μm to prepare a sample for immunochromatography. As beverage samples, milk and tea were purchased from a supermarket and used. These drinks were each suspended in PBS at a concentration of 1 / 10, and solid matter including bacteria was removed using a 0.45 μm filter to prepare samples for immunochromatography. Environmental samples were prepared by wiping the surfaces of hands, cutting boards, knives, and refrigerator handles using a commercially available wiping kit (ELMEX Pro·mediaST-25, PBS), suspending them in the PBS provided with the kit, and then removing solid matter including bacteria using a 0.45 μm filter to prepare samples for immunochromatography.

[0154] The immunochromatographic samples of various food and drink and environmental specimens prepared above were added to the sample addition member area of ​​each of the immunochromatographic detection kits (a) to (c) described above, and after 30 minutes, the line color development at the capture antibody application site of the membrane carrier was visually confirmed. The results are shown in Table 6. As intended, the detection kits (a) to (c) did not show cross-reactivity with the components in the above food and drink and environmental specimens. In combination with the above-mentioned examples, it was confirmed that the immunochromatographic detection kits (a) to (c) prepared by combining the above-mentioned general-purpose antibody and specific antibody do not react with non-bacterial components (food and drink and environmental components) in the above-mentioned food and drink and environmental specimens, and can simply and quickly detect only the multiple genera of bacteria to be detected with high selectivity. Similar results were obtained for the detection kits using the combinations (d) to (f) in Table 4 above.

[0155] [Table 6] [Industrial Applicability]

[0156] INDUSTRIAL APPLICABILITY The present invention can be widely used in fields requiring simultaneous and simple detection of multiple genera of bacteria in food and beverage, the environment, and biological samples, mainly in the fields of medicine and food and beverage, and is of extremely high industrial utility. [Explanation of symbols]

[0157] 10 Detection mechanism 1. Insoluble membrane carrier for chromatographic development 2. Detection antibody-impregnated member (conjugate pad) 3. Sample pad 4 Absorption materials (absorption pads) 5 Capture antibody immobilization site 6. Control reagent immobilization site Sample A B Sample flow

Claims

1. 1. A method for detecting the presence and / or abundance of bacteria in a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method includes a step of simultaneously detecting the presence and / or abundance of at least two or more different genera of bacteria in a sample based on an antigen-antibody reaction, the detection step includes a step of contacting a specimen with an antibody that undergoes an antigen-antibody reaction with a component derived from the two or more genera of bacteria, and a step of measuring the presence or absence and / or intensity of the antigen-antibody reaction occurring in the specimen after the contact, The method, wherein the antibody which undergoes an antigen-antibody reaction with a component derived from bacteria of said two or more genera is an antibody which undergoes an antigen-antibody reaction with ribosomal protein L7 / L12 of bacteria of said two or more genera.

2. 1. A method for detecting the presence and / or abundance of bacteria in a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method includes a step of simultaneously detecting the presence and / or abundance of at least two or more different genera of bacteria in a sample based on an antigen-antibody reaction, the detection step includes a step of contacting a specimen with an antibody that undergoes an antigen-antibody reaction with a component derived from the two or more genera of bacteria, and a step of measuring the presence or absence and / or intensity of the antigen-antibody reaction occurring in the specimen after the contact, The method further comprises the step of lysing bacteria in the specimen prior to contacting the specimen with the antibody.

3. The method according to claim 2, wherein the antibody that reacts with the component derived from the bacteria of the two or more genera is an antibody that reacts with the ribosomal protein L7 / L12 of the bacteria of the two or more genera.

4. 4. The method according to claim 1, wherein in the detection step, bacteria of two or more different genera selected from the group consisting of the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella are simultaneously detected.

5. The method according to any one of claims 1 to 4, wherein the two or more genera of bacteria to be detected include both Gram-negative bacteria and Gram-positive bacteria.

6. The method according to any one of claims 1 to 5, wherein in the detection step, bacteria of at least 3 or more, or 4 or more, or 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, or 10 or more, or 11 or more different genera are simultaneously detected.

7. The method according to any one of claims 1 to 6, wherein an antibody that undergoes an antigen-antibody reaction with components derived from bacteria of the two or more genera does not cross-react with one or more non-bacterial components that may be present in a sample.

8. The method according to claim 7, wherein the non-bacteria-derived components that do not cross-react with antibodies that cause an antigen-antibody reaction with the components derived from bacteria of the two or more genera are organic components derived from viruses, plants, and / or animals.

9. The method according to any one of claims 1 to 8, wherein the antibody that generates an antigen-antibody reaction with the components derived from the bacteria of two or more genera is a monoclonal antibody, a fragment thereof, or a derivative thereof.

10. The monoclonal antibody or a fragment thereof, or a derivative thereof, As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5; and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO:

6. The method of claim 9 , each comprising:

11. The monoclonal antibody or a fragment thereof, or a derivative thereof, A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:1, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:2, or A heavy chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 3, and a light chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 4, or A heavy chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:5, and a light chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:

6. The method of claim 10.

12. The method according to any one of claims 1 to 11, wherein the method comprises: (I) capturing bacteria in the specimen and labeling the bacteria in the specimen through an antigen-antibody reaction between the specimen, a capture antibody linked to a solid phase carrier, and a detection antibody having a detection label; and (II) A step of detecting the target bacteria in the sample based on the detection label. detecting the presence and / or amount of bacteria in a sample by A method in which one of the capture antibody and the detection antibody is one or more specific antibodies that undergo an antigen-antibody reaction with one or more types of target bacteria, and the other antibody is one or more general-purpose antibodies that undergo an antigen-antibody reaction with five or more genera of bacteria including the target bacteria.

13. 1. A method for detecting the presence and / or abundance of bacteria in a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method includes a step of simultaneously detecting the presence and / or abundance of at least two or more different genera of bacteria in a sample based on an antigen-antibody reaction, the detection step includes a step of contacting a specimen with an antibody that undergoes an antigen-antibody reaction with a component derived from the two or more genera of bacteria, and a step of measuring the presence or absence and / or intensity of the antigen-antibody reaction occurring in the specimen after the contact, The method further comprising: (I) capturing bacteria in the specimen and labeling the bacteria in the specimen through an antigen-antibody reaction between the specimen, a capture antibody linked to a solid phase carrier, and a detection antibody having a detection label; and (II) A step of detecting the target bacteria in the sample based on the detection label. detecting the presence and / or amount of bacteria in a sample by A method in which one of the capture antibody and the detection antibody is one or more specific antibodies that undergo an antigen-antibody reaction with one or more types of target bacteria, and the other antibody is one or more general-purpose antibodies that undergo an antigen-antibody reaction with five or more genera of bacteria including the target bacteria.

14. The step (I) (Ia-1) contacting a specimen with a detection antibody and labeling the bacteria in the specimen through an antigen-antibody reaction between the detection antibody and the bacteria; and (Ia-2) A step of contacting a specimen containing bacteria labeled with a detection antibody with a capture antibody and capturing the bacteria in the specimen by an antigen-antibody reaction between the capture antibody and the bacteria-detection antibody complex. The method of claim 12 or 13, comprising:

15. The step (I) (Ib-1) contacting a specimen with a capture antibody and capturing bacteria in the specimen through an antigen-antibody reaction between the capture antibody and the bacteria; and (Ib-2) A step of contacting a specimen containing the bacteria captured by the capture antibody with a detection antibody, and labeling the bacteria in the specimen by an antigen-antibody reaction between the detection antibody and the bacteria-capture antibody complex. The method of claim 12 or 13, comprising:

16. The method according to any one of claims 12 to 15, wherein the capture antibody is a general antibody and the detection antibody is a specific antibody.

17. The method according to any one of claims 12 to 15, wherein the detection antibody is a general antibody and the capture antibody is a specific antibody.

18. The method according to any one of claims 12 to 17, wherein the generic antibody reacts with five or more genera of bacteria selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

19. The method according to any one of claims 12 to 18, wherein the specific antibody specifically reacts with bacteria of one or more genera selected from at least the genera Escherichia, Staphylococcus, Pseudomonas, Bacillus, Klebsiella, Serratia, Rahnella, Citrobacter, Listeria, Enterobacter, and Salmonella.

20. A universal antibody As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 5; and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO:

6. The method according to any one of claims 12 to 19, each comprising:

21. A universal antibody A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:1, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:2, or A heavy chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 3, and a light chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 4, or A heavy chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:5, and a light chain variable region sequence has an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO:

6.

21. The method of claim 20.

22. The specific antibody is As a heavy chain variable region sequence, an amino acid sequence having 80% or more homology with at least one amino acid sequence selected from SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, and SEQ ID NO: 13, and As a light chain variable region sequence, an amino acid sequence having 80% or more homology with at least one of the amino acid sequences selected from SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, and SEQ ID NO:

14. The method according to any one of claims 12 to 21, each comprising:

23. The specific antibody is A heavy chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 7, and a light chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 8, or A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:9, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO:10, or A heavy chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 11, and a light chain variable region sequence having an amino acid sequence that is 80% or more identical to the amino acid sequence of SEQ ID NO: 12, or a heavy chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 13, and a light chain variable region sequence having an amino acid sequence having 80% or more homology with the amino acid sequence of SEQ ID NO: 14; 23. The method of claim 22.

24. A method for determining the degree of bacterial contamination of a sample selected from a food sample, an environmental sample, and a biological sample, comprising: The method comprises a step of simultaneously detecting the presence, absence and / or abundance of one or more genera of bacteria in the sample based on an antigen-antibody reaction by the method according to any one of claims 1 to 23.

25. A kit for detecting the presence and / or amount of bacteria in a sample selected from a food or beverage sample, an environmental sample, and a biological sample by the method according to any one of claims 1 to 11, the kit comprising an antibody according to any one of claims 1 to 11.

26. A kit for detecting the presence and / or amount of bacteria in a sample selected from a food and beverage sample, an environmental sample, and a biological sample, by the method according to any one of claims 12 to 23, the kit comprising a capture antibody and a detection antibody according to any one of claims 12 to 23, one of the capture antibody and the detection antibody being the general-purpose antibody and the other being the specific antibody.

27. The sample is allowed to spread and contact the sample with the capture antibody. A detection line having a capture antibody immobilized thereon is provided on the insoluble membrane carrier, 27. The kit of claim 26, configured to detect two or more types of bacteria in a sample at a single detection line.

28. The kit according to claim 26 or 27, wherein the kit is an immunochromatography kit.

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