JP6387500B2 - E. coli genotyping method and primer set used therefor - Google Patents

Description

  The present invention relates to a clone identification method and / or strain identification method of Escherichia coli and a primer set used therefor.

  Escherichia coli is an important pathogenic bacterium as a cause of various infectious diseases such as diarrhea and urinary tract infections. Among Escherichia coli, we acquired enterohemorrhagic Escherichia coli, which is a causative agent of food poisoning and causes serious infections such as hemolytic uremic syndrome, and third-generation cephalosporin resistance that causes nosocomial infections. There are also groups that are likely to be associated with mass infection, such as E. coli producing substrate-specific extended β-lactamase (ESBL).

  Examples of Escherichia coli having high pathogenicity include enterohemorrhagic Escherichia coli such as O157, and a group having many ESBL-producing bacteria includes Escherichia coli of sequence type 131 (ST131). Enterohemorrhagic Escherichia coli and drug-resistant bacteria often cause sporadic infectious diseases as well as mass infections such as food poisoning and nosocomial infections. Infection management is important, and it is necessary to identify the infection route. .

  On the other hand, Escherichia coli has a variety of genetic background strains, and even a group of enteropathogenic E. coli alone has several serotypes, and strains with different serotypes often have different sequence types. .

In order to identify the infection route when food poisoning or nosocomial infection is suspected, it is necessary to determine whether the strains isolated from different patients are the same. Therefore, the characteristics of the genome possessed by the strain are detected to identify the strain, which is called strain identification or genotype classification.
Conventionally, pulse field gel electrophoresis (hereinafter referred to as PFGE) has been frequently used as a method for classifying bacteria by genotype. PFGE is a method of cutting bacterial genomic DNA with restriction enzymes and determining the genotype of the strain as an electrophoretic pattern of its fragments. It has a high discrimination ability and is reproducible.

  However, PFGE takes about 3 days after the identification and identification of the strain at the earliest before results are obtained, and when the test results are obtained, the spread of infection is often already completed. In addition to the need to judge by comparing complex band patterns, the PFGE pattern of E. coli is likely to change, and even in the same population infection strain, the band pattern often changes over time. Subjective elements tend to be included. Therefore, an expert is required to determine whether the genotype is the same even for strains that have migrated at the same time. Therefore, it is very difficult to determine whether the genotypes of multiple isolates are equivalent by comparing the results of PFGE analysis obtained at different times or in different laboratories. In addition, the PFGE pattern of E. coli tends to change and tends to be difficult to determine. Furthermore, PFGE is cumbersome and requires skilled workers, and requires a special expensive device such as a pulse field gel electrophoresis apparatus, and the cost of reagents and the like is high. Therefore, there is still a strong demand for the development of a method that can classify E. coli widely and more simply and quickly.

  In order to overcome the problems of PFGE, an efficient typing method was devised by setting primers on the inside and outside of the inserted sequence and detecting the position of the mobile inserted sequence that exists in multiple copies in the genome. ing. The realization of the method using the insertion sequence is limited to the bacterial species or clones having multiple copies of the insertion sequence. In E. coli, only specific clones such as enterohemorrhagic Escherichia coli O157 and O26 can be realized, and in addition, O157 and O26. It is necessary to set the detection position for each serotype, and it is practically impossible to design a versatile primer.

  In addition, efforts have been made to detect ORFs having different holding states for each strain and to identify strains from the holding pattern. However, in the literature method, only enterohemorrhagic Escherichia coli O157 can be identified, and the versatility is poor (Non-patent Document 1).

  In addition, a method has been devised for efficient typing by repeatedly detecting sequences in many microorganisms. While it is possible to design a detection system with a high degree of versatility, it is necessary to accurately determine a slight difference in band size for reading the typing result, which is likely to cause erroneous determination.

  In E. coli, a phylogenetic group called phylogenetic group is also performed. To determine the phylogenetic group, three genes called chuA, yjaA, and TspE4.C2 are detected, and phylogenetic analysis is performed based on the possession pattern. However, the phylogenetic group analysis is intended to be roughly classified into four groups related to pathogenicity, and remains a supplementary role as a molecular epidemiological analysis (Non-patent Document 2).

  As described so far, it has been extremely difficult to develop a method for identifying E. coli strains in a general, quick and easy manner.

  As a molecular epidemiological method that is easy to implement and manage data, the method of detecting the reading frame (ORF) of a gene with different possession status for each strain and determining the genotype from the possession pattern is S. aureus, Pseudomonas aeruginosa, and Realized by Acinetobacter (Non-patent Document 3). In S. aureus and Pseudomonas aeruginosa, the method of determining the genotype from the ORF possession pattern is an appropriate combination of the ORF that constitutes the genomic islet that is a small insertion sequence and the ORF that constitutes the genomic island such as phage and pathogenic eyelined. The necessary genotyping method has been realized. There is a possibility that genotypes can be determined in the same way in E. coli, but there are various genomic islets and genomic islands found in the genome of E. coli that exist in nature. It is not clear whether a genotyping method that can be used for this is feasible.

  On the other hand, Patent Document 1 discloses a method for classifying S. aureus by genotype and a primer set used therein, and Patent Document 2 discloses a method for classifying Pseudomonas aeruginosa and a primer set used therefor. 3 describes a microorganism identification method, primers and identification kits used in the method, and Patent Document 4 describes a high-resolution typing system for pathogenic E. coli.

JP 2011-120528 A JP 2013-146244 A JP 2008-5837 A JP 2005-517396 A

Applied and Environmental Microbilogy 2011, 77: 2458-2470 Applied and Environmental Microbilogy 2000, 66: 4555-4558 Journal of Clinical Microbiology 2014, 52: 2925-2932

  Escherichia coli is a resident bacteria in humans, and some of its clones are highly pathogenic, and become invasive pathogenic bacteria including gastrointestinal symptoms, urinary tract infections, and sometimes sepsis. In addition, clones that have acquired antibacterial drug resistance have been found and are problematic in the medical field. Escherichia coli may cause mass infection such as food poisoning and nosocomial infection. In this case, molecular epidemiological analysis is necessary to identify the infection route and determine the scale of infection. Since the diversity of Escherichia coli is very high, in addition to determining whether the genotypes are identical or not, the genetic characterization of the strain causing the infection or outbreak is classified into any clone It is necessary to decide whether it is a stock.

  In view of the above circumstances, the present invention develops a technique for rapid identification of E. coli epidemic clones and strain identification, and identifies E. coli epidemic clones and / or strains more suitable for practical industrial (medical field) use. It aims to provide a method for identification. Another object of the present invention is to provide a primer set used in a method for identifying epidemic clones and / or strain identification.

  As a result of intensive studies to solve the above-mentioned problems, the present inventor compares the genetic information of E. coli that is being accumulated in the database, detects and selects a plurality of genes that reflect the clonal complex, and performs PCR on those genes. After the amplification in step 1, the clones of E. coli are roughly classified by comparing the migration pattern of the gene product by ordinary electrophoresis without determining the base sequence of the amplification product, and the investigation of the infection source when nosocomial infection occurs Successful identification at available strain level. Specifically, the present inventor detects (1) the ORF that constitutes a genomic islet on the chromosome and (2) the presence or absence of the ORF that constitutes the genomic island on the chromosome in any order, and It was found that clone classification and classification by genotype of E. coli can be performed more effectively by classifying by genotype according to the combination of presence or absence.

  That is, according to the present invention, on the genome of E. coli, (1) the ORF constituting the genomic islet and (2) the presence or absence of the ORF constituting the genomic island are detected in any order, and the combination of the presence or absence of these ORFs A method for clone identification and / or strain identification of E. coli comprising the step of performing genotyping is provided.

  In the E. coli clone identification method and / or strain identification method of the present invention, the ORF constituting the genomic islet of (1) is ECNA114_4208, EC55989_4085, EC55989_0018, ECNA114_1457, EC55989_1089, LF82_085, ECS4731, ECS2436, ECNA114_0460, ECS0053, EC55989_0068, EC55989_0636, EC55989_0699, EC55989_0830, EC55989_1577, EC55989_1649, EC55989_1821, EC55989_2719, EC55989_4248, EC55989_4374, EC55989_4548, ECNABU_c34730, ECS89114 Preferably, it is an gene of 1 type (more preferably at least 4 types, particularly preferably 10 types of ECNA114 — 4208, EC55989 — 4085, EC55989 — 0018, ECNA114 — 1457, EC55989 — 1089, LF82 — 085, ECS4731, ECS2436, ECNA114 — 0460 and ECS0053) In ECS1190, Z2415, Z1432, ECS3501, ECH74115_1587, EC55989_2129, Z1797, EC55989_2641, ECH74115_2877, ECH74115_1791, ECNA114_0874, EC55989_1406, ECNA114_2097, ECNA114_3979, EC644 SEQ ID NO: 66, ECH74115_3039, ECH74115_2899, ECH74115_3056, ECH74115_3024, Z2404, ECH74115_3237, ECS1189, Z1456, ECH74115_2915, Z2384, ECS1527, ECH74115_1860, Z1854, Z3358, Z3362,, EC55989_0314, EC55989_0547, EC55989_0685, EC55989_0762, EC55989_0766, EC55989_0799, EC55989_0805, EC55989_1022 , EC55989_1258, EC55989_1399, EC55989_1636, EC55989_2099, EC55989_2104, EC55989_2188, EC55989_2249, EC55989_2256, EC55989_2891, EC55989_3358, EC55989_3371, EC55989_3396, EC55989_3400, EC55989_3400, EC55989_3400 03, EC55989_4941, EC55989_4958, EC55989_4963, EC55989_4969, EC55989_4972, EC55989_5004, EC55989_5006, ECS0288, ECS0797, ECS0813, ECS1102, ECS1176, ECS1299, ECS1301, ECS1516, ECS1564, ECS1564, ECS1516 ECS2283, ECS2792, ECS2927, ECS2996, ECS4458, ECS5272, ECS5304, ECS5305, ECSF_3727, ECSF_4152, ECSF2757, S0692, S0913, S1482, S2103, S3222, S4314, S4832, SEQ ID NO: 68, SEQ ID NO: 68, SEQ ID NO: 68 No. 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, P423_16715c, P423_16735c, P423_16745c, P423_16780c, ECNA114_4753, P423_10825c, SEQ ID NO: 376, SEQ ID NO: 377, SEQ ID NO: 378, SEQ ID NO: 379 , SEQ ID NO: 380, SEQ ID NO: 381, SEQ ID NO: 382, SEQ ID NO: 383, SEQ ID NO: 384, SEQ ID NO: 385, SEQ ID NO: 386, SEQ ID NO: 387, SEQ ID NO: 388, SEQ ID NO: 389, SEQ ID NO: 390, Sequence No. 455, SEQ ID NO: 456, and at least one selected from the group consisting of SEQ ID NO: 461, more preferably at least 4, more preferably at least 8, particularly preferably ECS1190, Z2415, Z1432, ECS3501, ECH74115_1587, EC55989_2129, Z1797, EC55989_2641, ECH74115_2877, ECH74115_1791, ECNA114_0874, EC55989_1406, ECNA114_2097, ECNA114_3979, ECNA114_4026, S0497, ECNA114_1225, SEQ ID NO: 63, SEQ ID NO: 65, SEQ ID NO: 66, P423_10815c, 423 The 29 genes of SEQ ID NO: 381, SEQ ID NO: 389, SEQ ID NO: 390, and SEQ ID NO: 461 are preferable.

  Further, the clone identification method and / or strain identification method of the present invention includes SEQ ID NO: 1 and 2, SEQ ID NO: 3 and 4, SEQ ID NO: 5 and 6, SEQ ID NO: 7 and 8, SEQ ID NO: 9 and 10 or SEQ ID NOS: 413 and 414, SEQ ID NOS: 11 and 12, or SEQ ID NOS: 415 and 416, SEQ ID NOS: 13 and 14, or SEQ ID NOS: 417 and 418, SEQ ID NOS: 15 and 16, SEQ ID NOS: 17 and 18, or SEQ ID NOS: 419 and 420, A combination of 15 base sequences shown in SEQ ID NOs: 19 and 20 or SEQ ID NOs: 421 and 422 (provided that the base sequence has addition, substitution, deletion and / or insertion of 2 bases or less) The ORF of (1) above was detected by PCR using 10 sets of primers consisting of SEQ ID NO: 76 and 77, SEQ ID NO: 78 and 79, SEQ ID NO: 80 and 81, Nos. 82 and 83, SEQ ID Nos. 84 and 85, SEQ ID Nos. 86 and 87, SEQ ID Nos. 88 and 89, SEQ ID Nos. 90 and 91, SEQ ID Nos. 92 and 93, SEQ ID Nos. 94 and 95, SEQ ID Nos. 96 and 97, SEQ ID No. 98 And 99, SEQ ID NOS: 100 and 101 or SEQ ID NOS: 403 and 404, SEQ ID NOS: 102 and 103, SEQ ID NOS: 104 and 105, SEQ ID NOS: 106 and 107, SEQ ID NOS: 108 and 109, SEQ ID NOS: 110 and 111, or SEQ ID NOS: 391 and 392 , SEQ ID NO: 112 and 113, SEQ ID NO: 114 and 115, SEQ ID NO: 116 and 117, SEQ ID NO: 393 and 394, SEQ ID NO: 395 and 396, SEQ ID NO: 397 and 398, SEQ ID NO: 401 and 402, SEQ ID NO: 405 and 406, Sequence 31 sets of bases shown in Nos. 407 and 408, SEQ ID Nos. 462 and 463 and SEQ ID Nos. 464 and 465 The above-mentioned (by the above-mentioned base sequence may have addition, substitution, deletion and / or insertion of 2 or less bases), and the above ( It can be implemented by detecting the ORF of 2).

  As described above, the primer may have addition, substitution, deletion and / or insertion of 2 or less bases. From the viewpoint of classifying by genotype with high accuracy, the primer contains bases. Preferably there are no additions, substitutions, deletions and / or insertions.

  When a multiplex PCR method is employed as the PCR method, the cost of genotyping can be reduced.

If the detection results of presence / absence of ORF in (1) and (2) are replaced with 1 (yes) and 0 (no), respectively, and binary coding is performed, the detection results are digitized for easy viewing.
By further converting the binary encoding result to decimal encoding, the number of digits of the result is reduced, and the result can be more easily discriminated, and the result obtained in another date, other laboratory, etc. It is possible to make an accurate comparison.

  Further according to the present invention, SEQ ID NO: 1 and 2, SEQ ID NO: 3 and 4, SEQ ID NO: 5 and 6, SEQ ID NO: 7 and 8, SEQ ID NO: 9 and 10, or SEQ ID NO: 413 and 414, SEQ ID NO: 11 and 12 or SEQ ID NOS: 415 and 416, SEQ ID NOS: 13 and 14, or SEQ ID NOS: 417 and 418, SEQ ID NOS: 15 and 16, SEQ ID NOS: 17 and 18, or SEQ ID NOS: 419 and 420, SEQ ID NOS: 19 and 20, or SEQ ID NOS: 421 and 422 10 sets of primers and sequences comprising 15 combinations of the indicated base sequences (however, the above base sequence may have addition, substitution, deletion and / or insertion of 2 or less bases) Nos. 76 and 77, SEQ ID Nos. 78 and 79, SEQ ID Nos. 80 and 81, SEQ ID Nos. 82 and 83, SEQ ID Nos. 84 and 85, SEQ ID Nos. 86 and 87, SEQ ID Nos. 88 and 89, SEQ ID Nos. 90 and 91 SEQ ID NO: 92 and 93, SEQ ID NO: 94 and 95, SEQ ID NO: 96 and 97, SEQ ID NO: 98 and 99, SEQ ID NO: 100 and 101, SEQ ID NO: 403 and 404, SEQ ID NO: 102 and 103, SEQ ID NO: 104 and 105, SEQ ID NO: 106 and 107, SEQ ID NO: 108 and 109, SEQ ID NO: 110 and 111 or SEQ ID NO: 391 and 392, SEQ ID NO: 112 and 113, SEQ ID NO: 114 and 115, SEQ ID NO: 116 and 117, SEQ ID NO: 393 and 394, SEQ ID NO: 395 396, SEQ ID NOs: 397 and 398, SEQ ID NOs: 401 and 402, SEQ ID NOs: 405 and 406, SEQ ID NOS: 407 and 408, and SEQ ID NOs: 462 and 463, and 31 combinations of base sequences shown in SEQ ID NOs: 464 and 465 ( However, the above base sequence includes addition, substitution, deletion and / or insertion of bases of 2 bases or less. Including 29 pairs of primers consisting of even may) have been, genotyping classification primer set of E. coli is provided.

  As described above, the primer may have addition, substitution, deletion and / or insertion of 2 or less bases. From the viewpoint of classifying by genotype with high accuracy, the primer contains bases. Preferably there are no additions, substitutions, deletions and / or insertions.

  According to the present invention, clone identification and / or strain identification of E. coli can be carried out simply, quickly, objectively and with high sensitivity without requiring specialized equipment or operator skill. Molecular epidemiological analysis at the time of outbreak and the spread of the same strain due to nosocomial infection can be traced, and as a result, rapid spread of infection can be achieved.

FIG. 1 shows an electrophoretic photograph of Example 1. In FIG. 1, the numerical values described as “1 2...” Indicate the number of the isolate. FIG. 2 shows an electrophoresis photograph of Example 2. In FIG. 2, the numerical value described as “1 2...” Indicates the number of the isolate. FIG. 3 shows an electrophoresis photograph of Example 3. In FIG. 3, the numerical values described as “1 2...” Indicate the number of the isolate. FIG. 4 shows an electrophoresis photograph of Example 4. In FIG. 4, the numerical values such as “1 2...” Indicate the number of the isolate. FIG. 5 shows the electrophoresis photograph of Example 4. In FIG. 5, numerical values such as “1 2...” Indicate the number of the isolate. FIG. 6 shows an electrophoresis photograph of Example 4. In FIG. 6, the numerical values described as “1 2...” Indicate the number of the isolate. FIG. 7 shows the electrophoresis photograph of Example 5. In FIG. 7, a numerical value such as “25 26...” Indicates the number of the isolate. FIG. 8 shows the electrophoresis photograph of Example 6. In FIG. 8, a numerical value such as “49 50...” Indicates the number of the isolate. FIG. 9 shows the electrophoresis photograph of Example 7. In FIG. 9, the numerical values described as “71 72...” Indicate the numbers of the isolates. FIG. 10 shows the electrophoresis photograph of Example 7. In FIG. 10, numerical values such as “71 72...” Indicate the number of the isolate. FIG. 11 shows the electrophoresis photograph of Example 8. In FIG. 11, the numerical values described as “71 72...” Indicate the number of the isolate. FIG. 12 shows the electrophoresis photograph of Example 8. In FIG. 12, the numerical values such as “71 72...” Indicate the number of the isolate.

Hereinafter, the present invention will be specifically described.
The clone identification method of Escherichia coli and / or the strain identification method according to the present invention comprises: (1) an ORF constituting a genomic islet on the chromosome of E. coli; and (2) the presence or absence of an ORF constituting a genomic island. Including the step of detecting in order and classifying by genotype according to the combination of presence or absence of these ORFs, and the step of performing genotyping by a combination of presence or absence of different ORFs derived from these two types Yes. Hereinafter, these ORFs will be described.

[(1) ORF that composes genomic islet]
(Genetic characteristics of E. coli)
Multilocus sequence typing (MLST) analysis is used as a method for systematically classifying the genetic background of E. coli. For MLST analysis of E. coli, a method developed by Pasteur Institute, France, a method developed by Achtman et al. (Molecular Microbiology 2006, 60: 1136-1151) and a method developed by Whittam et al. (Www.shigatox.net) However, analysis was performed according to the method developed by Achtman et al.

  In MLST analysis, base sequences of seven housekeeping genes (adk, fumC, gyrB, icd, mdh, purA, recA) are determined, and sequence type (ST) is determined. In addition, by using a clonal complex (CC), which is a collection of closely related ST populations, it is possible to collect strains with the same genetic background, that is, clones, which are indispensable for epidemiological studies. In addition, S. aureus, Pseudomonas aeruginosa, and Acinetobacter showed that it is effective to detect the possession pattern of genomic islet to estimate CC, but is the same method effective in E. coli? It was unknown until now.

  Some E. coli have various genetic backgrounds. Genetic background survey results (including the results of detection of various ORFs) in actual wild strains can be used as fragmentary information in individual research facilities as documents, but by themselves, minimal ORFs are detected This is not enough to develop a clone identification method that can identify epidemic clones.

  Therefore, the present inventor collected clinically isolated Escherichia coli, performed MLST analysis, and investigated their genetic background. As a result, it has been found that there are various strains classified into CC in E. coli clinically isolated in Japan, and it is necessary to realize a strain distinguishability sufficient to identify CC in order to roughly classify the isolates. is there.

(ORF that composes genomic islet)
In order to distinguish the CC type, it has been found useful to detect ORFs constituting a genomic islet even in E. coli. Table 1 shows the genomic islet possession patterns of all genome analysis strains on the gene database. Genomic islet refers to the part where the sequence differs by about 5 kbp or less when comparing bacterial genomes, which are scattered throughout the genome and do not affect the survival probability of the individual. It is thought that it was left behind in the process of evolution.

  As can be seen from Table 1, the possession patterns of genomic islet (ECNA114_4208 to LF82_248) are different in different strains of E. coli ST type.

  Table 2 shows the results of investigating the status of genomic islet possession in clinical isolates.

By examining the pattern of detection of genomic islet in clinical isolates and selecting the optimal ORF, it is possible to detect a relatively small number of genomic islets, such as 10 or less, in clone identification and analysis of outbreaks that do not depend on a specific epidemic clone. Sufficient strain discrimination ability is obtained also in typing.

  For example, ECNA114_4208 is the 4208th gene of NA114 strain (Accession No. CP002797) published in GenBank, EC55989_4085 is the 4085th gene of E. coli 55989 strain (Accession No. CU928145), and LF82_085 is the LF82 strain ( Accession No.CU651637) 85th gene, ECS4731 means Sakai strain (Accession No.BA000007) 4731 gene, ECABU_c34730 means ABU83972 strain (Accession No.CP001671) 3473th gene However, this gene is not only present in the NA114 strain, E. coli 55989 strain, LF82 strain, Sakai strain, and ABU83972 strain, but may also be present in strains derived from this strain or in E. coli strains different from these strains. is there.

The gene ECNA114_4208 can be detected by PCR using primers of SEQ ID NO: 1 (forward) and 2 (reverse) in the sequence listing,
The gene EC55989_4085 can be detected by PCR using primers of SEQ ID NO: 3 (forward) and 4 (reverse) in the sequence listing,
The gene EC55989_0018 can be detected by PCR using the primers of SEQ ID NO: 5 (forward) and 6 (reverse) in the sequence listing,
Gene ECNA114_1457 can be detected by PCR using primers of SEQ ID NOs: 7 (forward) and 8 (reverse) in the sequence listing,
The gene EC55989_1089 can be detected by PCR using primers of SEQ ID NO: 9 (forward) and 10 (reverse) in the sequence listing, or primers of SEQ ID NO: 413 (forward) and 414 (reverse) in the sequence listing. ,
The gene LF82 — 085 can be detected by PCR using the primers of SEQ ID NO: 11 (forward) and 12 (reverse) in the sequence listing, or the primers of SEQ ID NO: 415 (forward) and 416 (reverse) in the sequence listing. ,
The gene ECS4731 can be detected by PCR using primers of SEQ ID NOs: 13 (forward) and 14 (reverse) of the sequence listing, or primers of SEQ ID NOs: 417 (forward) and 418 (reverse) of the sequence listing. ,
The gene ECS2436 can be detected by PCR using the primers of SEQ ID NO: 15 (forward) and 16 (reverse) in the sequence listing,
The gene ECNA114_0460 can be detected by PCR using primers of SEQ ID NOs: 17 (forward) and 18 (reverse) of the sequence listing, or primers of SEQ ID NOs: 419 (forward) and 420 (reverse) of the sequence listing. ,
The gene ECS0053 can be detected by PCR using primers of SEQ ID NO: 19 (forward) and 20 (reverse) in the sequence listing, or primers of SEQ ID NO: 421 (forward) and 422 (reverse) in the sequence listing. .

The gene EC55989_0068 can be detected by PCR using primers of SEQ ID NOs: 21 (forward) and 22 (reverse) in the sequence listing,
The gene EC55989_0189 can be detected by PCR using the primers of SEQ ID NO: 23 (forward) and 24 (reverse) in the sequence listing,
The gene EC55989_0636 can be detected by PCR using primers of SEQ ID NO: 25 (forward) and 26 (reverse) in the sequence listing,
The gene EC55989 — 0699 can be detected by PCR using primers of SEQ ID NOs: 27 (forward) and 28 (reverse) in the sequence listing,
The gene EC55989_0830 can be detected by PCR using the primers of SEQ ID NO: 29 (forward) and 30 (reverse) in the sequence listing,
Gene EC55989_1577 can be detected by PCR using primers of SEQ ID NOs: 31 (forward) and 32 (reverse) in the sequence listing,
The gene EC55989_1649 can be detected by PCR using primers of SEQ ID NOs: 33 (forward) and 34 (reverse) in the sequence listing,
Gene EC55989 — 1821 can be detected by PCR using primers of SEQ ID NOs: 35 (forward) and 36 (reverse) in the sequence listing,
The gene EC55989_2719 can be detected by PCR using primers of SEQ ID NOs: 37 (forward) and 38 (reverse) in the sequence listing,
The gene EC55989_4248 can be detected by PCR using primers of SEQ ID NO: 39 (forward) and 40 (reverse) in the sequence listing,
Gene EC55989_4374 can be detected by PCR using primers of SEQ ID NOs: 41 (forward) and 42 (reverse) in the sequence listing,
The gene EC55989_4548 can be detected by PCR using primers of SEQ ID NOs: 43 (forward) and 44 (reverse) in the sequence listing,
The gene ECABU_c34730 can be detected by PCR using primers of SEQ ID NOs: 45 (forward) and 46 (reverse) in the sequence listing,
The gene ECNA114_0007 can be detected by PCR using primers of SEQ ID NOs: 47 (forward) and 48 (reverse) in the sequence listing,
The gene ECNA114_0140 can be detected by PCR using the primers of SEQ ID NO: 49 (forward) and 50 (reverse) in the sequence listing,
The gene ECS0914 can be detected by PCR using the primers of SEQ ID NO: 51 (forward) and 52 (reverse) in the sequence listing,
The gene ECS3904 can be detected by PCR using the primers of SEQ ID NOs: 53 (forward) and 54 (reverse) in the sequence listing,
Gene ECS4280 can be detected by PCR using primers of SEQ ID NOs: 55 (forward) and 56 (reverse) in the sequence listing,
The gene ECS4300 can be detected by PCR using the primers of SEQ ID NO: 57 (forward) and 58 (reverse) in the sequence listing,
Gene ECS4827 can be detected by PCR using primers of SEQ ID NO: 59 (forward) and 60 (reverse) in the sequence listing,
The gene LF82_248 can be detected by PCR using the primers of SEQ ID NO: 61 (forward) and 62 (reverse) in the sequence listing.
By detecting the ORF, the CC type can be easily distinguished.

  In addition, when these are detected using PCR and electrophoresis described later, DNA is easily amplified and an extra band hardly appears.

  In the above, detection of the genomic islet ORF (1) by the PCR method has been mainly described. However, the genomic islet ORF (1) can be detected by other methods, for example, by hybridization. is there.

[(2) ORF composing genomic island]
Among Escherichia coli, there are known highly pathogenic clones such as enterohemorrhagic Escherichia coli O157 and clones with a high drug resistance gene possession rate such as ST131, which are known to easily cause mass infection. In order to investigate a group infection by clones that are likely to cause problems in such a group infection, a strain identification method that requires a higher discrimination ability than clone identification is required.

  In recent years, genome decoding has progressed, and gene clusters consisting of 5 to 100 foreign genes are found in E. coli. This cluster is called genomic island. In addition to lysogen phages, pathogenic islands and resistant islands, genomic islands include those with unknown functions. Each genomic island has a size of about 5 kbp or more and is composed of 5 to 100 ORFs. In many cases, E. coli genomic islands have a combination of ORFs in a mosaic pattern, and diversity in the composition of ORFs in the genomic islands.

  However, there are various strains of E. coli. The actual genotype survey results (including the detection results of various ORFs) in wild strains can be used as individual fragmentary information in the literature or genome base sequence database, but only this will detect the minimum ORF. It is not enough to develop a strain identification method for E. coli.

  Therefore, the present inventor uses public gene information about E. coli of GenBank, designs primers for detecting ORFs of many genomic islands, and about E. coli with various genetic backgrounds, The composition of the gene ORF was examined.

  As a result of repeated examination of whole genome data in strains registered in the genome database and experiments to confirm possession of ORF by clinical isolates, detection by combining several ORFs of the genomic island gene is extremely effective in distinguishing E. coli strains. Became clear.

  As a result, ECS1190, Z2415, Z1432, ECS3501, ECH74115_1587, EC55989_2129, Z1797, EC55989_2641, ECH74115_2877, ECH74115_1791, ECNA114_0874, EC55989_1406, ECNA114_2097, EC55989_40, ECNA114039, ECNA11463 , SEQ ID NO: 66, ECH74115_3039, ECH74115_2899, ECH74115_3056, ECH74115_3024, Z2404, ECH74115_3237, ECS1189, Z1456, ECH74115_2915, Z2384, ECS1527, ECH74115_1860, Z1854, Z3358, Z3360, EC EC55989_1022, EC55989_1258, EC55989_1399, EC55989_1636, EC55989_2099, EC55989_2104, EC55989_2589, EC55989_2249, EC55989_2559, EC55989_5591, EC55989_4396, EC55989_4396, EC55989_4396 989_4903, EC55989_4941, EC55989_4958, EC55989_4963, EC55989_4969, EC55989_4972, EC55989_5004, EC55989_5006, ECS0288, ECS0797, ECS0813, ECS1102, ECS1176, ECS1299, ECS1301, ECS1516, ECS1516, ECS1516, ECS1516, ECS1516 ECS2283, ECS2792, ECS2927, ECS2996, ECS4458, ECS5272, ECS5304, ECS5305, ECSF_3727, ECSF_4152, ECSF2757, S0692, S0913, S1482, S2103, S3222, S4314, S4832, SEQ ID NO: 68, SEQ ID NO: 68, SEQ ID NO: 68 No. 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, P423_10825c, P423_16715c, P423_16735c, P423_16745c, P423_16780c, ECNA114_4753, SEQ ID NO: 376, SEQ ID NO: 377, SEQ ID NO: 378, SEQ ID NO: 379 , SEQ ID NO: 380, SEQ ID NO: 381, SEQ ID NO: 382, SEQ ID NO: 383, SEQ ID NO: 384, SEQ ID NO: 385), SEQ ID NO: 386, SEQ ID NO: 387, SEQ ID NO: 388, SEQ ID NO: 389, SEQ ID NO: 390 SEQ ID NO: 455, when the target of detecting SEQ ID NO: 456 and SEQ ID NO: 461, the present inventors to be able to classify the strain of E. coli with high precision found. By detecting the above ORF, it is highly versatile and enables strain identification for a wide range of clones. By detecting all the ORFs that make up these genomic islands, maximum strain identification ability is achieved.

  For example, the ECS1190 is the 1190th gene of the Sakai strain (Accession No. BA000007) published in GenBank, Z2415 is the 2415th gene of the EDL933 strain (Accession No. AE005174), and ECH74115_1587 is the EC4115 strain (Accession No. CP001164) 1587th gene, EC55989_2129 is E. coli 55989 strain (Accession No. CU928145) 2129th gene, ECNA114_874 is NA114 strain (Accession No. CP002797) 874th gene, S0497 is Shigella flexneri 2a str The 497th gene of 2457T strain (Accession No. AE014073), ECSF_3727 is the 3727th gene of SE15 strain (Accession No. AP009378), and P423_16715c is the 3343th gene of JJ1886 strain (Accession No. CP006784) However, this gene is not only present in the Sakai strain, EDL933 strain, EC4115 strain, 55989 strain, NA114 strain, Shigella flexneri 2a str. 2457T strain, SE15 strain, and JJ1886 strain. When And, in some cases it does not have.

  Table 3 shows the genomic island possession pattern in all genome data strains. As can be seen from Table 3, different ORF composition patterns are obtained for each strain.

  Table 4 shows the ORF possession pattern constituting the genomic island in the whole genome data strain. As can be seen from Table 4, the ORFs constituting the genomic island listed in Table 4 are particularly effective for identifying strains of ST131 clones, and different ORF constitution patterns are obtained for each ST131 clone strain.

  Table 5 shows the results of investigating the state of genomic island possession in clinical isolates. In clinical isolates, the ORF possession pattern was specific to the strain. By investigating the detection pattern of genomic islands in clinical isolates and selecting the optimal ORF, when analyzing outbreaks in a wide variety of highly versatile clones, it is possible to type by detecting relatively small numbers of genomic islands of 12 or less. In addition, sufficient strain discrimination ability can be obtained.

  P423 — 10825c, P423 — 16715c, P423 — 16735c, P423 — 16745c, P423 — 16780c, ECNA114 — 4753, SEQ ID NO: 376, SEQ ID NO: 377, SEQ ID NO: 379, SEQ ID NO: 380, SEQ ID NO: 381, SEQ ID NO: 382, SEQ ID NO: 383, SEQ ID NO: 384, SEQ ID NO: 385), SEQ ID NO: 386, SEQ ID NO: 387, SEQ ID NO: 388, SEQ ID NO: 389, SEQ ID NO: 390, SEQ ID NO: 455, SEQ ID NO: 456, and SEQ ID NO: 461 were examined for the possession status of genomic islands The results are shown in Table 6. ORFs constituting the genomic island listed in Table 6 are particularly effective for strain identification of ST131 clones, and even in clinical isolates, the ORF possession pattern is specific to the strain. By examining the detection pattern of genomic islands in clinical isolates, combining with the ORFs that compose the above genomic islands, and selecting the optimal ORF, the analysis of population infection of ST131 clones, which are particularly problematic for drug-resistant bacteria, 15 Sufficient strain discrimination ability can be obtained even in typing by detecting relatively small numbers of genomic islands.

The gene ECS1190 can be detected by PCR using primers of SEQ ID NOs: 76 (forward) and 77 (reverse) in the sequence listing.
Gene Z2415 can be detected by PCR using primers of SEQ ID NOs: 78 (forward) and 79 (reverse) in the sequence listing,
The gene Z1432 can be detected by PCR using the primers of SEQ ID NOs: 80 (forward) and 81 (reverse) in the sequence listing,
Gene ECS3501 can be detected by PCR using primers of SEQ ID NO: 82 (forward) and 83 (reverse) in the sequence listing,
The gene ECH74115_1587 can be detected by PCR using primers of SEQ ID NO: 84 (forward) and 85 (reverse) in the sequence listing,
Gene Z1797 can be detected by PCR using the primers of SEQ ID NO: 86 (forward) and 87 (reverse) in the sequence listing,
The gene EC55989_2641 can be detected by PCR using the primers of SEQ ID NO: 88 (forward) and 89 (reverse) in the sequence listing,
The gene ECH74115_2877 can be detected by PCR using primers of SEQ ID NOs: 90 (forward) and 91 (reverse) in the sequence listing,
The gene ECH74115_1791 can be detected by PCR using primers of SEQ ID NOs: 92 (forward) and 93 (reverse) in the sequence listing,
The gene ECNA114_0874 can be detected by PCR using primers of SEQ ID NO: 94 (forward) and 95 (reverse) in the sequence listing,
Gene EC55989_1406 can be detected by PCR using primers of SEQ ID NO: 96 (forward) and 97 (reverse) in the sequence listing, or primers of SEQ ID NO: 399 (forward) and 400 (reverse) in the sequence listing. ,
The gene ECNA114_2097 can be detected by PCR using primers of SEQ ID NO: 98 (forward) and 99 (reverse) in the sequence listing, or primers of SEQ ID NO: 411 (forward) and 412 (reverse) in the sequence listing. ,
The gene EC55989_2129 can be detected by PCR using primers of SEQ ID NOs: 100 (forward) and 101 (reverse) in the sequence listing, or primers of SEQ ID NOs: 403 (forward) and 404 (reverse) in the sequence listing. ,
The gene ECNA114_3979 can be detected by PCR using primers of SEQ ID NOs: 102 (forward) and 103 (reverse) of the sequence listing, or primers of SEQ ID NOs: 409 (forward) and 410 (reverse) of the sequence listing. ,
Gene ECNA114_4026 can be detected by PCR using primers of SEQ ID NOs: 104 (forward) and 105 (reverse) in the sequence listing,
Gene S0497 can be detected by PCR using primers of SEQ ID NOs: 106 (forward) and 107 (reverse) in the sequence listing,
The gene ECNA114 — 1225 can be detected by PCR using primers of SEQ ID NOs: 108 (forward) and 109 (reverse) in the sequence listing,
SEQ ID NO: 63 can be detected by PCR using the primers of SEQ ID NO: 110 (forward) and 111 (reverse) in the sequence listing, or the primers of SEQ ID NO: 391 (forward) and 392 (reverse) in the sequence listing. Yes,
SEQ ID NO: 64 is detectable by PCR using the primers of SEQ ID NO: 112 (forward) and 113 (reverse) in the sequence listing,
SEQ ID NO: 65 can be detected by PCR using the primers of SEQ ID NO: 114 (forward) and 115 (reverse) in the sequence listing,
SEQ ID NO: 66 can be detected by PCR using the primers of SEQ ID NO: 116 (forward) and 117 (reverse) in the sequence listing,
The gene ECH74115_3039 can be detected by PCR using primers of SEQ ID NO: 118 (forward) and 119 (reverse) in the sequence listing,
The gene ECH74115_2899 can be detected by PCR using primers of SEQ ID NOs: 120 (forward) and 121 (reverse) in the sequence listing,
Gene ECH74115_3056 can be detected by PCR using primers of SEQ ID NO: 122 (forward) and 123 (reverse) in the sequence listing,
The gene ECH74115_3024 can be detected by PCR using primers of SEQ ID NOs: 124 (forward) and 125 (reverse) in the sequence listing,
The gene Z2404 can be detected by PCR using the primers of SEQ ID NO: 126 (forward) and 127 (reverse) in the sequence listing,
Gene ECH74115_3237 can be detected by PCR using primers of SEQ ID NO: 128 (forward) and 129 (reverse) in the sequence listing,
The gene ECS1189 can be detected by PCR using primers of SEQ ID NOs: 130 (forward) and 131 (reverse) in the sequence listing,
Gene Z1456 can be detected by PCR using primers of SEQ ID NOs: 132 (forward) and 133 (reverse) in the sequence listing,
Gene ECH74115_2915 can be detected by PCR using primers of SEQ ID NOs: 134 (forward) and 135 (reverse) in the sequence listing,
Gene Z2384 can be detected by PCR using the primers of SEQ ID NO: 136 (forward) and 137 (reverse) in the sequence listing,
The gene ECS1527 can be detected by PCR using primers of SEQ ID NOs: 138 (forward) and 139 (reverse) in the sequence listing,
The gene ECH74115_1860 can be detected by PCR using primers of SEQ ID NOs: 140 (forward) and 141 (reverse) in the sequence listing,
The gene Z1854 can be detected by PCR using the primers of SEQ ID NOs: 142 (forward) and 143 (reverse) in the sequence listing,
Gene Z3358 can be detected by PCR using primers of SEQ ID NOs: 144 (forward) and 145 (reverse) in the sequence listing,
Gene Z3362 can be detected by PCR using primers of SEQ ID NOs: 146 (forward) and 147 (reverse) in the sequence listing,
The gene EC55989_0314 can be detected by PCR using primers of SEQ ID NOS: 148 (forward) and 149 (reverse) in the sequence listing,
The gene EC55989_0547 can be detected by PCR using primers of SEQ ID NOs: 150 (forward) and 151 (reverse) in the sequence listing,
The gene EC55989_0685 can be detected by PCR using primers of SEQ ID NOs: 152 (forward) and 153 (reverse) in the sequence listing,
Gene EC55989_0762 can be detected by PCR using primers of SEQ ID NOs: 154 (forward) and 155 (reverse) in the sequence listing,
Gene EC55989_0766 can be detected by PCR using primers of SEQ ID NOs: 156 (forward) and 157 (reverse) in the sequence listing,
The gene EC55989_0799 can be detected by PCR using primers of SEQ ID NOs: 158 (forward) and 159 (reverse) in the sequence listing,
The gene EC55989 — 0805 can be detected by PCR using primers of SEQ ID NOs: 160 (forward) and 161 (reverse) in the sequence listing, and the gene EC55989 — 1022 is SEQ ID NO: 162 (forward) and 163 (reverse) in the sequence listing. The gene EC55989_1258 can be detected by PCR using the primers of SEQ ID NO: 164 (forward) and 165 (reverse) in the sequence listing, and the gene EC55989_1399 is It can be detected by PCR using the primers of SEQ ID NO: 166 (forward) and 167 (reverse) in the sequence listing, and the gene EC55989_1636 uses the primers of SEQ ID NO: 168 (forward) and 169 (reverse) in the sequence listing Detected by PCR The gene EC55989 — 2099 can be detected by PCR using the primers of SEQ ID NO: 170 (forward) and 171 (reverse) in the sequence listing, and the gene EC55989 — 2104 can be detected by SEQ ID NO: 172 (forward) and 173 in the sequence listing. By using the (reverse) primer, it can be detected by PCR,
The gene EC55989_2188 can be detected by PCR using primers of SEQ ID NOs: 174 (forward) and 175 (reverse) in the sequence listing,
The gene EC55989_2249 can be detected by PCR using primers of SEQ ID NOs: 176 (forward) and 177 (reverse) in the sequence listing,
The gene EC55989_2256 can be detected by PCR using primers of SEQ ID NOs: 178 (forward) and 179 (reverse) in the sequence listing,
Gene EC55989_2311 can be detected by PCR using primers of SEQ ID NOs: 180 (forward) and 181 (reverse) in the sequence listing,
The gene EC55989_3358 can be detected by PCR using the primers of SEQ ID NO: 182 (forward) and 183 (reverse) in the sequence listing,
Gene EC55989_3371 can be detected by PCR using primers of SEQ ID NOs: 184 (forward) and 185 (reverse) in the sequence listing,
The gene EC55989_3396 can be detected by PCR using the primers of SEQ ID NO: 186 (forward) and 187 (reverse) in the sequence listing,
The gene EC55989_3400 can be detected by PCR using primers of SEQ ID NOs: 188 (forward) and 189 (reverse) in the sequence listing,
The gene EC55989_3509 can be detected by PCR using the primers of SEQ ID NO: 190 (forward) and 191 (reverse) in the sequence listing,
The gene EC55989_4034 can be detected by PCR using the primers of SEQ ID NO: 192 (forward) and 193 (reverse) in the sequence listing,
The gene EC55989_4038 can be detected by PCR using primers of SEQ ID NOs: 194 (forward) and 195 (reverse) in the sequence listing,
The gene EC55989_4041 can be detected by PCR using primers of SEQ ID NOs: 196 (forward) and 197 (reverse) in the sequence listing,
The gene EC55989_4278 can be detected by PCR using the primers of SEQ ID NO: 198 (forward) and 199 (reverse) in the sequence listing,
Gene EC55989_4878 can be detected by PCR using primers of SEQ ID NOs: 200 (forward) and 201 (reverse) in the sequence listing,
Gene EC55989_4903 can be detected by PCR using primers of SEQ ID NOs: 202 (forward) and 203 (reverse) in the sequence listing,
Gene EC55989_4941 can be detected by PCR using primers of SEQ ID NOs: 204 (forward) and 205 (reverse) in the sequence listing,
The gene EC55989_4958 can be detected by PCR using the primers of SEQ ID NO: 206 (forward) and 207 (reverse) in the sequence listing,
Gene EC55989_4963 can be detected by PCR using primers of SEQ ID NOs: 208 (forward) and 209 (reverse) in the sequence listing,
The gene EC55989_4969 can be detected by PCR using primers of SEQ ID NO: 210 (forward) and 211 (reverse) in the sequence listing,
The gene EC55989_4972 can be detected by PCR using the primers of SEQ ID NO: 212 (forward) and 213 (reverse) in the sequence listing,
Gene EC55989_5004 can be detected by PCR using primers of SEQ ID NOs: 214 (forward) and 215 (reverse) in the sequence listing,
The gene EC55989_5006 can be detected by PCR using primers of SEQ ID NOs: 216 (forward) and 217 (reverse) in the sequence listing,
The gene ECS0288 can be detected by PCR using primers of SEQ ID NOs: 218 (forward) and 219 (reverse) in the sequence listing,
The gene ECS0797 can be detected by PCR using the primers of SEQ ID NO: 220 (forward) and 221 (reverse) in the sequence listing,
The gene ECS0813 can be detected by PCR using the primers of SEQ ID NO: 222 (forward) and 223 (reverse) in the sequence listing,
Gene ECS1102 can be detected by PCR using primers of SEQ ID NOs: 224 (forward) and 225 (reverse) in the sequence listing,
The gene ECS1176 can be detected by PCR using the primers of SEQ ID NO: 226 (forward) and 227 (reverse) in the sequence listing,
The gene ECS1299 can be detected by PCR using primers of SEQ ID NOs: 228 (forward) and 229 (reverse) in the sequence listing,
Gene ECS1301 can be detected by PCR using primers of SEQ ID NOs: 230 (forward) and 231 (reverse) in the sequence listing,
Gene ECS1516 can be detected by PCR using primers of SEQ ID NOs: 232 (forward) and 233 (reverse) in the sequence listing,
The gene ECS1564 can be detected by PCR using primers of SEQ ID NOs: 234 (forward) and 235 (reverse) in the sequence listing,
Gene ECS1592 can be detected by PCR using primers of SEQ ID NOs: 236 (forward) and 237 (reverse) in the sequence listing,
The gene ECS1597 can be detected by PCR using primers of SEQ ID NOs: 238 (forward) and 239 (reverse) in the sequence listing,
The gene ECS1662 can be detected by PCR using the primers of SEQ ID NO: 240 (forward) and 241 (reverse) in the sequence listing,
The gene ECS1663 can be detected by PCR using the primers of SEQ ID NOs: 242 (forward) and 243 (reverse) in the sequence listing,
The gene ECS1694 can be detected by PCR using primers of SEQ ID NOs: 244 (forward) and 245 (reverse) in the sequence listing,
The gene ECS1933 can be detected by PCR using primers of SEQ ID NOs: 246 (forward) and 247 (reverse) in the sequence listing,
The gene ECS1937 can be detected by PCR using primers of SEQ ID NOs: 248 (forward) and 249 (reverse) in the sequence listing,
The gene ECS2171 can be detected by PCR using the primers of SEQ ID NO: 250 (forward) and 251 (reverse) in the sequence listing,
The gene ECS2283 can be detected by PCR using the primers of SEQ ID NO: 252 (forward) and 253 (reverse) in the sequence listing,
Gene ECS2792 can be detected by PCR using primers of SEQ ID NOs: 254 (forward) and 255 (reverse) in the sequence listing,
The gene ECS2927 can be detected by PCR using primers of SEQ ID NO: 256 (forward) and 257 (reverse) in the sequence listing,
The gene ECS2996 can be detected by PCR using the primers of SEQ ID NO: 258 (forward) and 259 (reverse) in the sequence listing,
The gene ECS4458 can be detected by PCR using primers of SEQ ID NO: 260 (forward) and 261 (reverse) in the sequence listing,
The gene ECS5272 can be detected by PCR using the primers of SEQ ID NO: 262 (forward) and 263 (reverse) in the sequence listing,
Gene ECS5304 can be detected by PCR using primers of SEQ ID NOs: 264 (forward) and 265 (reverse) in the sequence listing,
The gene ECS5305 can be detected by PCR using the primers of SEQ ID NO: 266 (forward) and 267 (reverse) in the sequence listing,
The gene ECSF — 3727 can be detected by PCR using primers of SEQ ID NOs: 268 (forward) and 269 (reverse) in the sequence listing,
The gene ECSF — 4152 can be detected by PCR using primers of SEQ ID NOs: 270 (forward) and 271 (reverse) in the sequence listing,
The gene ECSF2757 can be detected by PCR using the primers of SEQ ID NO: 272 (forward) and 273 (reverse) in the sequence listing,
Gene S0692 can be detected by PCR using primers of SEQ ID NOs: 274 (forward) and 275 (reverse) in the sequence listing,
The gene S0913 can be detected by PCR using primers of SEQ ID NOs: 276 (forward) and 277 (reverse) in the sequence listing,
Gene S1482 can be detected by PCR using primers of SEQ ID NOs: 278 (forward) and 279 (reverse) in the sequence listing,
Gene S2103 can be detected by PCR using primers of SEQ ID NOs: 280 (forward) and 281 (reverse) in the sequence listing,
Gene S3222 can be detected by PCR using primers of SEQ ID NOs: 282 (forward) and 283 (reverse) in the sequence listing,
The gene S4314 can be detected by PCR using primers of SEQ ID NOs: 284 (forward) and 285 (reverse) in the sequence listing,
The gene S4832 can be detected by PCR using primers of SEQ ID NOs: 286 (forward) and 287 (reverse) in the sequence listing,
By using the primers of SEQ ID NO: 287 (forward) and 289 (reverse) in SEQ ID NO: 67 Sequence Listing, it can be detected by PCR,
SEQ ID NO: 68 can be detected by PCR using the primers of SEQ ID NO: 290 (forward) and 291 (reverse) in the sequence listing,
SEQ ID NO: 69 can be detected by PCR using the primers of SEQ ID NO: 292 (forward) and 293 (reverse) in the Sequence Listing,
SEQ ID NO: 70) can be detected by PCR using the primers of SEQ ID NO: 294 (forward) and 295 (reverse) in the sequence listing,
SEQ ID NO: 71 can be detected by PCR using the primers of SEQ ID NO: 296 (forward) and 297 (reverse) in the sequence listing,
SEQ ID NO: 72 can be detected by PCR using primers of SEQ ID NO: 298 (forward) and 299 (reverse) in the sequence listing,
SEQ ID NO: 73 can be detected by PCR using the primers of SEQ ID NO: 300 (forward) and 301 (reverse) in the sequence listing,
SEQ ID NO: 74 can be detected by PCR using the primers of SEQ ID NO: 302 (forward) and 303 (reverse) in the sequence listing,
SEQ ID NO: 75 can be detected by PCR using the primers of SEQ ID NO: 304 (forward) and 305 (reverse) in the sequence listing.

The gene P423 — 16715c can be detected by PCR using the primers of SEQ ID NO: 397 (forward) and SEQ ID NO: 398 (reverse) in the sequence listing,
The gene P423_16735c can be detected by PCR using the primers of SEQ ID NO: 423 (forward) and SEQ ID NO: 424 (reverse) in the sequence listing,
The gene P423_16745c can be detected by PCR using primers of SEQ ID NO: 425 (forward) and SEQ ID NO: 426 (reverse) in the sequence listing,
The gene P423_16780c can be detected by PCR using the primers of SEQ ID NO: 427 (forward) and SEQ ID NO: 428 (reverse) in the sequence listing,
Gene P423_10825c can be detected by PCR using primers of SEQ ID NO: 464 (forward) and SEQ ID NO: 465 (reverse) in the sequence listing,
The gene ECNA114_4753 can be detected by PCR using the primers of SEQ ID NO: 429 (forward) and SEQ ID NO: 430 (reverse) in the sequence listing,
SEQ ID NO: 376 can be detected by PCR using the primers of SEQ ID NO: 407 (forward) and SEQ ID NO: 408 (reverse) in the sequence listing,
SEQ ID NO: 377 can be detected by PCR using primers of SEQ ID NO: 431 (forward) and SEQ ID NO: 432 (reverse) in the sequence listing,
SEQ ID NO: 378 can be detected by PCR using primers of SEQ ID NO: 433 (forward) and SEQ ID NO: 434 (reverse) in the sequence listing,
SEQ ID NO: 379 can be detected by PCR using primers of SEQ ID NO: 435 (forward) and SEQ ID NO: 436 (reverse) in the sequence listing,
SEQ ID NO: 380 can be detected by PCR using primers of SEQ ID NO: 401 (forward) and SEQ ID NO: 402 (reverse) in the sequence listing,
SEQ ID NO: 381 can be detected by PCR using the primers of SEQ ID NO: 393 (forward) and SEQ ID NO: 394 (reverse) in the sequence listing,
SEQ ID NO: 382 can be detected by PCR using primers of SEQ ID NO: 437 (forward) and SEQ ID NO: 438 (reverse) in the sequence listing,
SEQ ID NO: 383 can be detected by PCR using primers of SEQ ID NO: 439 (forward) and SEQ ID NO: 440 (reverse) in the sequence listing,
SEQ ID NO: 384 can be detected by PCR using the primers of SEQ ID NO: 441 (forward) and SEQ ID NO: 442 (reverse) in the sequence listing,
SEQ ID NO: 385 can be detected by PCR using primers of SEQ ID NO: 443 (forward) and SEQ ID NO: 444 (reverse) in the sequence listing,
SEQ ID NO: 386 can be detected by PCR using primers of SEQ ID NO: 445 (forward) and SEQ ID NO: 446 (reverse) in the sequence listing,
SEQ ID NO: 387 can be detected by PCR using primers of SEQ ID NO: 447 (forward) and SEQ ID NO: 448 (reverse) in the sequence listing,
SEQ ID NO: 388 can be detected by PCR using primers of SEQ ID NO: 449 (forward) and SEQ ID NO: 450 (reverse) in the sequence listing,
SEQ ID NO: 389 can be detected by PCR using primers of SEQ ID NO: 405 (forward) and SEQ ID NO: 406 (reverse) in the sequence listing,
SEQ ID NO: 390 can be detected by PCR using primers of SEQ ID NO: 395 (forward) and SEQ ID NO: 396 (reverse) in the sequence listing,
SEQ ID NO: 455 can be detected by PCR using the primers of SEQ ID NO: 451 (forward) and SEQ ID NO: 452 (reverse) in the sequence listing,
SEQ ID NO: 456 can be detected by PCR using primers of SEQ ID NO: 453 (forward) and SEQ ID NO: 454 (reverse) in the sequence listing,
SEQ ID NO: 461 can be detected by PCR using the primers of SEQ ID NO: 462 (forward) and SEQ ID NO: 463 (reverse) in the sequence listing.

  In addition, when these are detected using PCR and electrophoresis described later, DNA is easily amplified and an extra band hardly appears.

  In the above, the detection of the ORF (2) constituting the genomic island by the PCR method has been mainly described. However, the ORF (2) constituting the genomic island can be detected by other methods, for example, hybridization. Can be detected.

[ORF detection means]
The above-described detection of the presence or absence of the ORF (1) constituting the genomic islet and the ORF (2) constituting the genomic island on the chromosome of E. coli can be performed in any order. Specifically, these ORFs may be detected in any order for each ORF, or may be detected collectively in any order for a plurality of ORFs, or all ORFs may be detected simultaneously. Good. Means for detecting the ORF include PCR and hybridization.

<PCR>
When detecting separately for each ORF, for example, using a set of primers (forward primer and reverse primer) corresponding to each ORF to be detected, together with an E. coli DNA extraction sample in an independent system, Real time PCR reaction is performed to detect the signal generated from PCR amplification products in real time.

  In addition, when detecting a plurality of ORFs collectively, for example, a primer for detecting yhbX (e.g., equivalent to EC55989_3592 of E. coli 55989 strain) as an E. coli marker was added (SEQ ID NOs: 306 and 307 in the sequence listing). Multiplex PCR in which a plurality of sets of primers (a set of forward primer and reverse primer) respectively corresponding to a plurality of ORFs are mixed and placed in the same reaction system to perform a PCR reaction can be performed. In this case, the presence or absence of a PCR amplification product corresponding to each ORF is confirmed by the presence or absence of a band obtained by electrophoresis of the solution after the reaction by electrophoresis, for example, agarose gel electrophoresis or capillary electrophoresis.

When all ORFs are detected simultaneously, for example, a microarray is applied to detect the ORF. For detection using a microarray, probes that hybridize with each ORF are prepared in each well of the microarray, DNA purified from the culture by column extraction or phenol-chloroform extraction is hybridized, and unreacted DNA is allowed to migrate. After washing, the target ORF can be detected by labeling with a fluorescent dye that binds to double-stranded DNA and measuring with a machine that captures fluorescence.
Among these, multiplex PCR is preferable because a plurality of ORFs can be efficiently and collectively detected by a simple technique.

(Primer design)
As for ORF (1) that constitutes the above genomic islet and ORF (2) that constitutes the genomic island, ORFs with a base sequence of about 90% are found on clinical isolates and databases. By designing a primer in a portion with few mutations so that it can be detected, the primer can be used universally for most E. coli that are often clinically isolated and is not susceptible to mutation.

  In addition to ORF (1) that constitutes the above genomic islet and ORF (2) that constitutes the genomic island, it corresponds to each of a primer for detecting yhbX as an E. coli marker, a primer for determining the phylogenetic group, and a primer for detecting drug resistance genes. When designing a primer to be used, the primer itself bends to form a double strand by binding to each other, or different primers to bind to each other at a portion that is complementary to each other. The arrangement is such that it does not form a body or more.

  Furthermore, in consideration of detection by multiplex PCR, it is preferable that the primer GC ratio is about 50% and that the Tm value is matched. Further, it is desirable to adjust the amplification efficiency so that the PCR amplification product size is about 50 bp to 700 bp, preferably 70 bp to 600 bp so that separation can be performed in a short time during electrophoresis. In the ORF detected in the same reaction system, it is important to design primers so that the PCR amplification products do not have the same size.

  By setting the conditions as described above, it is possible to obtain primers and primer sets that can obtain highly reproducible amplification results in multiplex PCR. Such primers can be designed using commercially available software or software that is freely available through the web, but it depends on the interaction between ORFs that are detected simultaneously from the many primer candidates output by the software. In order to verify the deterioration of the amplification efficiency and the optimization of the amplification efficiency of each ORF, the optimal primers were found by trial and error using clinical isolates.

Specifically, as described in the ORF items (1) to (2) above,
(1) 36 sets of primers as primers for the ORF that constitutes the genomic islet
(2) A total of 180 primers (SEQ ID NOs: 1 to 62, 76 to 305, 391 to 454, and 462 to 465 in the sequence listing) of 144 sets of primers as primers for ORF constituting the genomic island, the present inventor Designed.

  When multiplex PCR is performed using the above primer set, primers for detecting yhbX as a marker of Escherichia coli in 10 primer sets (SEQ ID NO. 306 and 307) and 14 primers combined with primers (SEQ ID NOs: 308 and 309, SEQ ID NOs: 310 and 311 and SEQ ID NOs: 312 and 313 in the sequence listing) for determining the phylogenetic group as a large genotype classification of E. coli As shown in Table 8 below as a primer mixture, 11 primer pairs obtained by adding yhbX as an E. coli marker (SEQ ID NOs: 306 and 307 in the sequence listing) to 10 primer sets As shown in Table 9 below as a primer mixture, 12 primer sets were added to the large intestine. 13 pairs of primers to which yhbX was detected as a marker (SEQ ID NOs: 306 and 307 in the sequence listing) were added, and yhbX was detected as an E. coli marker in 11 sets of primers as shown in the primer mixture in Table 10 below. Primers (SEQ ID NOs: 306 and 307 in the Sequence Listing), and primers for detecting yhbX as a marker for E. coli in 9 primer sets as shown in Table 11 below as a primer mixture (Sequence Listing) SEQ ID NOs: 306 and 307), and 12 sets of primers (SEQ ID NOs: 457 and 458 and SEQ ID NOs: 459 and 460) for detecting drug resistance genes (CTX-M-1 group and CTX-M-9 group) It is desirable to carry out PCR in a reaction system in which the above primers are combined and mixed. In addition, clone identification and strain identification may be performed simultaneously or separately. In the case of enterohemorrhagic Escherichia coli and various clones of Escherichia coli, strain identification may be performed by using only one of the primer set shown in Table 8 or the primer set shown in Table 9, respectively. In addition to the primer sets shown in Tables 8 and 9, it is effective to simultaneously perform the primer sets shown in Tables 10 and 11 for identifying strains of ST131 clones. SEQ ID NOs: 100 and 101 are included in both primer sets shown in Tables 6 and 7, and SEQ ID NOS: 1 and 2 and SEQ ID NOS: 3 and 4 are included in both primer sets shown in Tables 7 and 10. SEQ ID NOs: 106 and 107 are included in both of the primer sets shown in Table 9 and Table 10, and SEQ ID NOs: 94 and 95 and SEQ ID NOs: 104 and 105 are included in both of the primer sets shown in Table 9 and Table 11. included.

Note that yhbX of the amplified ORF represented by SEQ ID NOs: 306 and 307 is a gene encoding hydrolase and is universally found in E. coli, and can be used as a common marker for identifying E. coli.

  The specific primers shown above are sequences optimized for amplifying the target ORF, and even if these primers have changes such as addition, substitution, deletion and / or insertion of about 2 bases, The function as a primer is not lost, and the target ORF can be amplified by PCR. Addition means that a base is added to the 5 'or 3' end of the primer shown in the table, and insertion means not between the above ends but between the base and the base inside the primer. Say that a base is added.

  From the viewpoint of exerting high performance as a primer, the change is preferably addition, substitution, deletion, or insertion of 2 bases or less, and addition of 2 bases or less, or 5 ′ side or 3 ′ side of 2 bases or less. Is more preferable, and addition of a base complementary to the target ORF of 1 base or less or deletion of 1 base or less at the 5′-end or 3′-end is particularly preferable. In general, changes on the 5 'side do not easily lose the function as a primer, and changes on the 3' side tend to lose the function of the primer.

<Hybridization>
When detecting ORF by hybridization, first, DNA purified from a culture (E. coli) by column extraction or phenol-chloroform extraction is alkali-denatured and fixed on a nylon membrane, cellulose membrane or microplate. Probes are prepared that hybridize with each ORF detected by the present invention. The probe may be artificially synthesized DNA or may be prepared by PCR using the primers described above. The probe is labeled using biotin, digoxigenin, a fluorescent dye, or the like. The bacteria-extracted DNA is hybridized with the probe, and according to the label of the probe, enzyme addition, color development, light emission, etc. are performed to capture the signal. This is performed for each detected ORF.

[Clone identification by ORF detection and strain identification method]
In the following, multiplex PCR is performed, and among the ORFs (1) to (2) above, the ORF preferable as the detection target is detected as an example, and the clone identification method and strain identification method of the present invention are used. Explain the procedure.

(Identification of bacterial species)
Use a medium that can separate Escherichia coli, such as blood agar medium (for general bacterial separation), MacConkey medium, etc. from patient-derived specimens such as stool, blood, urine, etc., or medical instruments such as catheters and gauze To isolate E. coli-like bacteria. Then, it identifies with colon_bacillus | E._coli by confirmation of the form by Gram dyeing | staining, and confirmation of biochemical property.

  A strain identified as Escherichia coli can be transformed into a liquid medium capable of growing E. coli (Luria-Bertani broth, Brain Heart Infusion medium, tryptic soy bouillon, etc.), or an agar medium (Luria-Bertani agar medium, Brain Heart Infusion agar medium, Incubate overnight at 37 ° C using tryptic soy agar, normal agar, etc.

(DNA extraction)
From cultured cells, heat extraction, phenol extraction, DNA extraction using a commercially available DNA extraction kit, or heat extraction obtained by suspending and heating cells in distilled water or Tris-EDTA buffer, etc. Extract and use as a sample (template) for PCR reaction.

(PCR reaction)
In addition to 10 ORFs constituting the genomic islet and 29 ORFs constituting the genomic island described in Tables 7, 8, 9, 10 and 11 above in multiplex PCR, yhbX as an Escherichia coli marker, and chuA as a Phylogenetic group detection site , YjaA and TspE4.C2 and drug resistance genes (CTX-M-1 group and CTX-M-9 group) are detected. Specifically, the number of primer sets (forward primer and reverse primer) corresponding to the ORF group to be detected is divided into 5 groups of 14 sets, 11 sets, 13 sets, 12 sets, and 12 sets. Perform PCR reaction in batches in the same reaction tube. In addition, clone identification and strain identification may be performed simultaneously or separately.

(Electrophoresis)
The PCR amplification product is electrophoresed using a gel such as an agarose gel under conditions such that DNA fragments of approximately 50 bp to 600 bp are sufficiently separated. The migration distance may be about 5 to 6 cm, and in the case of a minigel, it can be sufficiently separated at 100 V for about 60 minutes. After electrophoresis, take photographs by staining with ethidium bromide or cyber green. In addition, PCR products can be separated and imaged using various capillary electrophoresis apparatuses such as Agilent 2100 Bioanalyzer and Shimadzu MultiNA.

(Result judgment)
A maximum of 14, 11, 13, 12, or 12 bands appear respectively. Since the band size is known in advance in the genotyping method of the present invention, it is determined whether or not there is a band of the desired size in each strain and reaction system. In some cases, non-specific bands other than the target size may appear, but the non-specific bands are ignored. A binary code is created with a band of the desired size (a band corresponding to each ORF and a band corresponding to a positive control) being 1 if no amplification is seen.

  This code may be created for each ORF of (1) to (2), or all may be created as a single code, or the ORFs of (1) to (2) Some of them may be created together. When the clone identification method of the present invention is used in an actual medical field, if all ORFs (1) to (2) are collectively created as one code, the number of digits becomes large and difficult to see. Several ORF results are preferably generated as a single code.

  Here, as described above, E. coli is easy to understand when combined into a clonal complex (CC) type for genotype classification, and is useful for identifying epidemic clones. The possession pattern of the ORF in (1) has a high correlation with the CC type and is useful for estimating the CC. By comparing the ORF possession patterns of (2), strain identification becomes possible.

  Therefore, it is preferable to create the ORF detection result of (1) as one code, and it is preferable to create the ORF detection result of (2) as one, two, or three codes, respectively. Considering this, it is more preferable to create three codes.

  Then, for example, in order to make the binary code created in this way easier to see by reducing the number of digits, it is converted into, for example, a decimal system to obtain a genotype code. An example of the above code creation is shown in Table 12 and Table 13 below. The examples in Table 12 use the primer sets described in Tables 7, 8 and 9 for the EDL933 strains in Tables 1 and 3. The examples in Table 13 use the primer sets described in Table 10 and Table 11 for the NA114 strains in Tables 1, 3 and 4.

  The primer set shown in Table 8 has high strain discrimination ability particularly in enterohemorrhagic E. coli, and the primer set shown in Table 9 exhibits strain discrimination ability in a wide range of clones of E. coli other than enterohemorrhagic E. coli. In addition, the primer sets shown in Table 10 and Table 11 exhibit a high strain discrimination ability against ST131 clones at the same time as the clones are roughly classified, but the detection ORFs listed in Tables 8, 9, 10 and 11 are They are not limited to enterohemorrhagic E. coli and ST131, but can be used in all clones. If the detected serotype of E. coli is known by dividing the primer set as shown in Table 8, Table 9, Table 10, and Table 11, Table 8, Table 9, Table 10, or Table 11 is used. The required effect can be obtained by simply implementing any one of the primer sets shown in the above.

  First, the presence or absence of each ORF in E. coli to be tested is detected by PCR and electrophoresis using appropriate primers, and encoded by the binary method. This code is converted into a decimal system to obtain a genotype code. In the example of Table 12, the code is 429-476-19-1, and in the example of Table 13, the code is 71-20-166.

In the examples shown in Tables 12 and 13, since Code 1 and Code 5 summarize the ORF detection results of (1), when genotype codes are generated for a plurality of E. coli strains, It becomes a numerical value equivalent to. From this numerical value, it is possible to determine the clonality equivalent to MLST. The combination of code 2 and code 3 and code 4 and code 6 and the code 7 is a specific code strains can be divided into computationally 2 ²⁹ kinds of genotypes. Code 2 is selected for ORF to enhance the ability to distinguish strains in enterohemorrhagic Escherichia coli. Code 3 and code 4 are selected for ORF to enhance the ability to identify strains in Escherichia coli other than enterohemorrhagic Escherichia coli. In many clones, strain identification is possible. Code 6 and code 7 are effective in identifying strains of drug-resistant Escherichia coli because the ORF is selected so that the strain discrimination ability of ST131 clone is high.

  Specifically, for example, if the presence or absence of 10 ORFs (1) (ECNA114_4208 to ECS0053) in 24 Escherichia coli clinical isolates is binary-encoded and further decimal-encoded as described above, Table 14 below.

In Table 14, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth and fifth rows from the top are the sequences by MLST analysis. type (ST) type and clonal complex (CC) type. In addition, O157: H7 of strain numbers 16-19 are all ST11, CC11, O26: H11 or O26: HNM of strain numbers 20-22 are all ST21, CC29, O111: H- of strain numbers 23 and 24 are all ST16, Considered CC29.
When the determination results are encoded in this way, genetically related strains and strains with the same serotype have the same value, and the related relationship is understood. Even when a serotype based on commercially available serum cannot be determined, a highly versatile data can be obtained because a genotype is obtained. Furthermore, by comparing the obtained genotype codes, it is possible to easily and objectively identify strains isolated at different times and facilities.

  Further, (2) ORFs constituting code 2 among ORFs constituting genomic islands are detected as shown in Table 15.

In Table 15, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth and fifth rows from the top are the Sequence type by MLST analysis. (ST) type and clonal complex (CC) type.
The 24 strains were subdivided into 19 genotypes.

  Further, (2) ORFs constituting code 3 and code 4 among ORFs constituting a genomic island are detected as shown in Table 16.

In Table 16, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth row from the top is the Sequence type (ST ) Type.
The 24 strains were subdivided into 19 genotypes.

Specifically, for example, Code 5, Code 6 and Code 7 in the combination of (1) ORF composing genomic islet and (2) ORF composing genomic island in 24 E. coli clinical isolates centered on ST131. Table 17 shows the detection of ORFs constituting the.

In Table 17, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth and fifth rows from the top are the sequences by MLST analysis. type (ST) type and clonal complex (CC) type.
In addition, it is thought that all the strains of strain numbers 55, 57-60, and 75-87 are ST131. In addition, 17 strains considered to be the same clone (ST131) were subdivided into 14 genotypes.
Thus, by combining (1) the ORF constituting the genomic islet and (2) the ORF constituting the genomic island, clone identification and strain identification can be performed simultaneously.

Furthermore, most of the ORFs to be detected in the present invention are ORFs not related to the pathogenicity of E. coli. Genes with specific functions, such as those related to virulence, may increase the probability that the E. coli will grow in the host, or the gene product will be the target of the host immune system and conversely reduce the probability of survival. There is. In other words, such genes are thought to be possessed by many of E. coli, or vice versa. In the present invention, appropriate ORFs are selected and genotype classification is performed so that such a bias is not applied.
EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example, this invention is not limited to these Examples.

Example 1
A total of 24 strains of enterohemorrhagic Escherichia coli, Escherichia coli clinically isolated in hospitals, and Escherichia coli isolated from healthy subjects were classified by genotype by ORF detection according to the following procedure.

<Clone identification by ORF detection>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  14 sets of primers were combined and one reaction tube was used, and multiplex PCR was performed on 14 ORFs. The primer combinations and their final concentrations are as shown in Table 18 below.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 14 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIG.

  In Table 9, as described above, related strains are found from the code. For example, strains 1, 2, and 3 are ST131, which is considered to have many ESBL-producing bacteria because the code is 587. In addition, O157: H7 of strain numbers 16-19 are all ST11, CC11, O26: H11 or O26: HNM of strain numbers 20-22 are all ST21, CC29, and O111: H- of strain numbers 23 and 24 are all ST16, Considered CC29.

Example 2
A total of 24 E. coli strains as in the previous example were classified by genotype by ORF detection according to the following procedure.
<Strain identification by ORF detection (code 2)>
(Culture of E. coli)
24 clinically isolated enterohemorrhagic Escherichia coli strains were cultured overnight at 37 ° C. using tryptic soy agar medium.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  11 sets of primers were combined and one reaction tube was used, and multiplex PCR was performed on 11 ORFs. The primer combinations and their final concentrations are as shown in Table 19 below.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 11 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIG.

In Table 15, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth row from the top is the Sequence type by MLST analysis. (ST) type. The 24 strains were subdivided into 19 genotypes.

Example 3
A total of 24 E. coli strains as in the previous example were classified by genotype by ORF detection according to the following procedure.

<Strain identification by ORF detection (codes 3 and 4)>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  13 sets of primers were combined and one reaction tube was used, and multiplex PCR was performed on 13 ORFs. The combinations of primers and their final concentrations are as shown in Table 20 below.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 13 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIG.

In Table 16, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth row from the top is the Sequence type (ST ) Type.
The 24 strains were subdivided into 19 genotypes.

Example 4
Hereinafter, an example in which the primer sequence is changed by about 2 bases will be described more specifically.
The same 24 strains of E. coli as in the previous example were classified by genotype by ORF detection according to the following procedure.
<Example when primer sequence is changed by about 2 bases>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  The primer was 14 sets, 11 sets, or 13 sets, and 3 reaction tubes were used, and multiplex PCR was performed on 38 ORFs. The primer combinations (primer mixtures 1, 2 and 3) and their final concentrations are shown in Table 21, Table 22 and Table 23 below.

  SEQ ID NO: 314 is a substitution of 1 base to SEQ ID NO: 1, SEQ ID NO: 315 is a addition of 2 bases to SEQ ID NO: 2, and SEQ ID NO: 316 is 2 bases to SEQ ID NO: 3 SEQ ID NO: 317 is a substitution of 1 base and deletion of 1 base with respect to SEQ ID NO: 4, SEQ ID NO: 318 is a substitution of 1 base with respect to SEQ ID NO: 5 SEQ ID NO: 319 is a substitution of 1 base with respect to SEQ ID NO: 6, SEQ ID NO: 320 is a deletion of 1 base with respect to SEQ ID NO: 7, and SEQ ID NO: 321 is relative to SEQ ID NO: 8. 1 base substitution, SEQ ID NO: 322 is a 1 base substitution and 1 base deletion from SEQ ID NO: 9, SEQ ID NO: 323 is a 1 base addition and 1 base to SEQ ID NO: 10 A base substitution, SEQ ID NO: 324 is the addition of 2 bases to SEQ ID NO: 11, SEQ ID NO: 325 is SEQ ID NO: 1 base addition to 1 base and 1 base substitution, SEQ ID NO: 326 is 1 base substitution to SEQ ID NO: 13, SEQ ID NO: 327 is 1 base substitution to SEQ ID NO: 14 SEQ ID NO: 328 is a 2 base addition to SEQ ID NO: 15, SEQ ID NO: 329 is a 2 base addition to SEQ ID NO: 16, SEQ ID NO: 330 is a sequence deletion 1 base addition and 1 base deletion to number 17; SEQ ID NO: 331 is a 1 base substitution and 1 base deletion to SEQ ID NO: 18; SEQ ID NO: 332 is a sequence SEQ ID NO: 333 is a deletion of 1 base from SEQ ID NO: 20 and a deletion of 1 base from SEQ ID NO: 20. 1 base addition and 1 base substitution, SEQ ID NO: 335 is a deletion of 2 bases from SEQ ID NO: 77, SEQ ID NO: No. 336 is a substitution of 2 bases to SEQ ID NO: 78, SEQ ID NO: 337 is a 1 base addition to SEQ ID NO: 79, SEQ ID NO: 338 is a 2 base addition to SEQ ID NO: 80 SEQ ID NO: 339 is a 1 base substitution and 1 base deletion from SEQ ID NO: 81, SEQ ID NO: 340 is a 2 base substitution from SEQ ID NO: 82 SEQ ID NO: 341 is a substitution of 1 base to SEQ ID NO: 83, SEQ ID NO: 342 is a substitution of 2 bases to SEQ ID NO: 84, and SEQ ID NO: 343 is 1 to SEQ ID NO: 85. SEQ ID NO: 344 is a substitution of 1 base and deletion of 1 base relative to SEQ ID NO: 100, SEQ ID NO: 345 is a addition of 2 bases to SEQ ID NO: 101 SEQ ID NO: 346 is a substitution of 2 bases to SEQ ID NO: 86, and SEQ ID NO: 347 is 2 to SEQ ID NO: 87. SEQ ID NO: 348 is a substitution of 1 base with respect to SEQ ID NO: 88, SEQ ID NO: 349 is a substitution of 1 base and deletion of 1 base with respect to SEQ ID NO: 89 Yes, SEQ ID NO: 350 is an addition of 1 base to SEQ ID NO: 90, SEQ ID NO: 351 is an addition of 1 base and 1 base substitution to SEQ ID NO: 91, SEQ ID NO: 352 is a sequence No. 92 is a substitution of 1 base, SEQ ID NO: 353 is a substitution of 1 base and deletion of 1 base to SEQ ID NO: 93, SEQ ID NO: 354 is 2 SEQ ID NO: 355 is a substitution of 2 bases to SEQ ID NO: 95, SEQ ID NO: 356 is a substitution of 1 base and a deletion of 1 base to SEQ ID NO: 96 Yes, SEQ ID NO: 357 is the addition of 2 bases to SEQ ID NO: 97, SEQ ID NO: 358 is 1 to SEQ ID NO: 98 1 base addition and 1 base substitution, SEQ ID NO: 359 is 1 base addition and 1 base substitution for SEQ ID NO: 99, SEQ ID NO: 360 is 2 bases for SEQ ID NO: 102 SEQ ID NO: 361 is a 2 base substitution for SEQ ID NO: 103, SEQ ID NO: 362 is a 1 base addition and 1 base substitution for SEQ ID NO: 104, SEQ ID NO: 363 is an addition of 1 base and 1 base substitution to SEQ ID NO: 105, SEQ ID NO: 364 is a substitution of 2 bases to SEQ ID NO: 106, SEQ ID NO: 365 is SEQ ID NO: 107 In contrast, SEQ ID NO: 366 has 2 base substitutions for SEQ ID NO: 108, SEQ ID NO: 367 has 1 base addition and 1 base substitution for SEQ ID NO: 109 SEQ ID NO: 368 is an insertion of one base relative to SEQ ID NO: 110, SEQ ID NO: 369 SEQ ID NO: 111 is a substitution of 2 bases, SEQ ID NO: 370 is an addition of 1 base and 1 base substitution to SEQ ID NO: 112, SEQ ID NO: 371 is 1 to SEQ ID NO: 113 SEQ ID NO: 372 is a 1 base addition to SEQ ID NO: 114, SEQ ID NO: 373 is a 2 base replacement for SEQ ID NO: 115. SEQ ID NO: 374 is obtained by adding 1 base and replacing 1 base to SEQ ID NO: 116, and SEQ ID NO: 375 is obtained by deleting 2 bases from SEQ ID NO: 117.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 14 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIGS. Results similar to those of FIGS. 1, 2 and 3, Tables 14, 15 and 16 were obtained.

Example 5
<Strain identification of enterohemorrhagic Escherichia coli>
(Culture of E. coli)
Twenty-four clinically isolated enterohemorrhagic Escherichia coli strains including 18 strains derived from 2 cases of mass infection were cultured overnight at 37 ° C. using tryptic soy agar medium.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  11 sets of primers were combined and one reaction tube was used, and multiplex PCR was performed on 11 ORFs. Table 19 shows primer combinations and final concentrations thereof.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 11 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIG.

In Table 24, the top row is the strain number, the second row from the top is the O serotype, and the third row from the top is the H serotype. The 24 strains were subdivided into 9 genotypes. Of the 24 strains, strain numbers 26, 28, 30, 32, 34, 36, 38, 39, 40, 41, 42, 43, 44, 45, 46 and 47, and strain numbers 25 and 33 are the same group infection cases. It can be seen that they belong to the same genotype.

Example 6
Genotype classification by ORF detection was performed for the total 24 strains of E. coli including 7 strains derived from 3 cases of mass infection clinically isolated in hospital and E. coli corresponding to ST131 isolated from healthy individuals according to the following procedure.

<Strain identification of ST131 clone>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  13 sets of primers were combined and one reaction tube was used, and multiplex PCR was performed on 13 ORFs. Table 20 shows primer combinations and final concentrations thereof.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 13 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIG.

  In Table 25, the top row is the strain number. The 24 strains were subdivided into 14 genotypes. Of the 24 strains, strain numbers 51, 53 and 55, strain numbers 52 and 54, and strain numbers 68 and 70 are bacteria collected from the same case of mass infection, but are found to belong to the same genotype.

Example 7
<Clone identification and strain identification of ST131 clone>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.

(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  Two sets of primers were combined and two reaction tubes were used, and multiplex PCR was performed on 23 ORFs. Tables 26 and 27 show primer combinations and final concentrations thereof.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 12 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed when amplification is observed. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIGS.

In Table 17, the top row is the strain number.
In Table 17, the top row is the strain number, the second row from the top is the O serotype, the third row from the top is the H serotype, and the fourth and fifth rows from the top are the sequences by MLST analysis. type (ST) type and clonal complex (CC) type.
The 24 strains were classified into 5 types of clones. In addition, it is thought that all the strains of strain numbers 55, 57-60, and 75-87 are ST131. In addition, 17 strains considered to be the same clone (ST131) were subdivided into 14 genotypes.
Thus, by combining (1) the ORF constituting the genomic islet and (2) the ORF constituting the genomic island, clone identification and strain identification can be performed simultaneously.

Example 8
Hereinafter, examples where the primer sequences shown in Table 10 and Table 11 are changed by about 2 bases will be described more specifically.
The same E. coli 24 strains as in Example 7 were classified by genotype by ORF detection according to the following procedure.
<Example when primer sequence is changed by about 2 bases>
(Culture of E. coli)
Twenty-four strains identified as E. coli were cultured overnight at 37 ° C. using tryptic soy agar.
(DNA extraction)
An amount corresponding to approximately one colony of the cultured bacteria was suspended in 100 μl of Tris-EDTA buffer in a 1.5 ml Eppendorf tube and heated at 100 ° C. for 10 minutes. Next, the tube was centrifuged at 12,000 rpm for 3 minutes, and the supernatant was used as a DNA heat extraction sample.

(Preparation of PCR reaction solution)
Roche's FastStart DNA polymerase was used according to the instructions. At that time, the reaction volume was 20 μl. The composition of the reaction solution 20 μl is 10 × FastStart Taq Buffer (containing MgCl ₂ ) 2 μl, 10 mM dNTP Mix 0.4 μl, 25 mM MgCl ₂ 0.8 μl, FastStart Taq DNA polymerase 0.2 μl, distilled water 14.2 μl, and primer mixture 0.4 μl . 2 μl (1/10 volume of the reaction solution) of the above-mentioned DNA heat extraction sample was added thereto.

  Two sets of primers were combined and two reaction tubes were used, and multiplex PCR was performed on 23 ORFs. The primer combinations and their final concentrations are shown in Tables 28 and 29.

  SEQ ID NO: 466 is a substitution of 1 base with respect to SEQ ID NO: 413, SEQ ID NO: 467 is a substitution of 1 base with respect to SEQ ID NO: 414, and SEQ ID NO: 468 is a base with respect to SEQ ID NO: 415 SEQ ID NO: 469 is a substitution of 1 base and deletion of 1 base from SEQ ID NO: 416, and SEQ ID NO: 470 is a deletion of 1 base from SEQ ID NO: 417. Yes, SEQ ID NO: 471 is the one with 1 base addition and 1 base substitution for SEQ ID NO: 418, SEQ ID NO: 472 is the one with 1 base substitution for SEQ ID NO: 419, SEQ ID NO: 473 is the sequence SEQ ID NO: 474 is obtained by adding 1 base and replacing 1 base by SEQ ID NO: 421. SEQ ID NO: 475 is obtained by adding 1 base to SEQ ID NO: 422. Of SEQ ID NO: 47 6 is an addition of 1 base to SEQ ID NO: 391, SEQ ID NO: 477 is a substitution of 1 base to SEQ ID NO: 392, SEQ ID NO: 478 is an addition of 1 base to SEQ ID NO: 393 SEQ ID NO: 479 is the addition of 1 base and 1 base substitution to SEQ ID NO: 394, SEQ ID NO: 480 is the addition of 2 bases to SEQ ID NO: 462, 481 is a substitution of SEQ ID NO: 463 with 2 bases, SEQ ID NO: 482 is a substitution of 1 base and deletion of 1 base with respect to SEQ ID NO: 395, SEQ ID NO: 483 is SEQ ID NO: 396 In contrast, SEQ ID NO: 484 is a one base substitution for SEQ ID NO: 464, and SEQ ID NO: 485 is a one base addition and one base substitution for SEQ ID NO: 465. SEQ ID NO: 486 is paired with SEQ ID NO: 401 SEQ ID NO: 487 is a 1 base replacement for SEQ ID NO: 402, SEQ ID NO: 488 is a 1 base addition and 1 base replacement for SEQ ID NO: 403 SEQ ID NO: 489 is an addition of 1 base and 1 base substitution to SEQ ID NO: 404, SEQ ID NO: 490 is a deletion of 2 bases from SEQ ID NO: 405, SEQ ID NO: 491 Is the addition of 1 base to SEQ ID NO: 406, SEQ ID NO: 492 is the addition of 1 base and substitution of 1 base to SEQ ID NO: 407, and SEQ ID NO: 493 is the addition of SEQ ID NO: 408 1 base deleted, SEQ ID NO: 494 is a 1 base substitution for SEQ ID NO: 397, SEQ ID NO: 495 is a 1 base addition and 1 base substitution for SEQ ID NO: 398 It is.

(PCR reaction)
Set the heat extracted DNA and reaction mixture in a thermal cycler (Applied Biosytems, GeneAmp PCR System 9700), first treat at 95 ° C for 4 minutes, then 95 ° C for 30 seconds, 60 ° C for 30 seconds, The cycle at 72 ° C for 90 seconds was repeated 30 times, and then a final extension at 72 ° C for 7 minutes was performed. After completion of the cycle reaction, the PCR product was stored at 4 ° C.

(Electrophoresis)
Using agarose gel (4% NuSieve 3: 1 in TBE buffer), a minigel was prepared, and 5 μl of PCR product was electrophoresed at 120 V for 60 minutes. The migration distance was about 5 cm. After electrophoresis, it was stained with ethidium bromide and photographed.

(Result judgment)
A maximum of 12 bands appeared per reaction. It is determined whether or not there is a band of the target size in each strain and reaction system. If the band of the target size is amplified, 1 is set, and 0 is not observed, and the same as in Table 12 above. A binary code was created. Further, the binary code was converted to the decimal system to obtain a genotype code.
The results are shown in FIGS. The same results as in FIGS. 9 and 10 and Table 17 were obtained.

Claims (11)

On the chromosome of E. coli,
(1) ORF that constitutes a genomic islet, and (2) ORF that constitutes a genomic island,
A method for clone identification and / or strain identification of E. coli, comprising the step of detecting the presence or absence of any of them in any order and classifying them according to the combination of the presence or absence of these ORFs,
The E. coli is ST10, ST11, ST15, ST16, ST17, ST21, ST35, ST46, ST57, ST59, ST73, ST93, ST94, ST95, ST127, ST131, ST135, ST155, ST156, ST354, ST357, ST414, ST597, E. coli selected from ST648, ST678, ST1060 and ST1132,
The genomic islet in the ORF of (1) is ECNA114_4208, EC55989_4085, EC55989_0018, ECNA114_1457, EC55989_1089, LF82_085, ECS4731, ECS2436, ECNA114_0460, ECS0053, EC55989_0068, EC55989_0189, EC55989_0869, EC55989_8989, EC55989_8989 , EC55989_4374, EC55989_4548, ECABU_c34730, ECNA114_0007, ECNA114_140, ECS0914, ECS3904, ECS4280, ECS4300, ECS4827 and LF82_248, and at least one gene selected from the group consisting of
The genomic islands in the ORF of (2) are ECS1190, Z2415, Z1432, ECS3501, ECH74115_1587, EC55989_2129, Z1797, EC55989_2641, ECH74115_2877, ECH74115_1791, ECNA114_0874, EC55989_1406, ECNA114_2097, ECNA114_79, ECNA114_793 SEQ ID NO: 65, SEQ ID NO: 66, ECH74115_3039, ECH74115_2899, ECH74115_3056, ECH74115_3024, Z2404, ECH74115_3237, ECS1189, Z1456, ECH74115_2915, Z2384, ECS1527, ECH74115_1860, Z1854, Z3358, EC2 EC55989_0805, EC55989_1022, EC55989_1258, EC55989_1399, EC55989_1636, EC55989_2099, EC55989_2104, EC55989_2188, EC55989_2249, EC55989_2256, EC55989_2231, EC55989_3358, EC55989_3961, EC5593 5989_4878, EC55989_4903, EC55989_4941, EC55989_4958, EC55989_4963, EC55989_4969, EC55989_4972, EC55989_5004, EC55989_5006, ECS0288, ECS0797, ECS0813, ECS1102EC, ECS1176, ECS1176, ECS1176 ECS2171, ECS2283, ECS2792, ECS2927, ECS2996, ECS4458, ECS5272, ECS5304, ECS5305, ECSF_3727, ECSF_4152, ECSF2757, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, P423 — 16715c, P423 — 16735c, P423 — 16745c, P423 — 16780c, ECNA114 — 4753, P423 — 10825c, SEQ ID NO: 376, SEQ ID NO: 377, SEQ ID NO: 378, SEQ ID NO: 379, SEQ ID NO: 380, SEQ ID NO: 381, SEQ ID NO: 382, SEQ ID NO: 383, SEQ ID NO: 384, SEQ ID NO: 385, SEQ ID NO: 386, SEQ ID NO: 387, SEQ ID NO: 388, SEQ ID NO: 389, SEQ ID NO: 390, SEQ ID NO: 455, SEQ ID NO: 456, At least one gene selected from the group consisting of finely SEQ ID NO: 461,
Method. The genomic islet in the ORF of (1) is ECNA114_4208, EC55989_4085, EC55989_0018, ECNA114_1457, EC55989_1089, LF82_085, ECS4731, ECS2436, ECNA114_0460, ECS0053, EC55989_0068, EC55989_0189, EC55989_0869, EC55989_8989, EC55989_8989 The clone identification method and / or strain of Escherichia coli according to claim 1, which is at least four genes selected from the group consisting of EC55989_4374, EC55989_4548, ECABU_c34730, ECNA114_0007, ECNA114_140, ECS0914, ECS3904, ECS4280, ECS4300, ECS4827 and LF82_248 Method for identification. The genomic islands in the ORF of (2) are ECS1190, Z2415, Z1432, ECS3501, ECH74115_1587, EC55989_2129, Z1797, EC55989_2641, ECH74115_2877, ECH74115_1791, ECNA114_0874, EC55989_1406, ECNA114_2097, ECNA114_79, ECNA114_793 SEQ ID NO: 65, SEQ ID NO: 66, ECH74115_3039, ECH74115_2899, ECH74115_3056, ECH74115_3024, Z2404, ECH74115_3237, ECS1189, Z1456, ECH74115_2915, Z2384, ECS1527, ECH74115_1860, Z1854, Z3358, EC2 EC55989_0805, EC55989_1022, EC55989_1258, EC55989_1399, EC55989_1636, EC55989_2099, EC55989_2104, EC55989_2188, EC55989_2249, EC55989_2256, EC55989_2231, EC55989_3358, EC55989_3961, EC5593 5989_4878, EC55989_4903, EC55989_4941, EC55989_4958, EC55989_4963, EC55989_4969, EC55989_4972, EC55989_5004, EC55989_5006, ECS0288, ECS0797, ECS0813, ECS1102EC, ECS1176, ECS1176, ECS1176 ECS2171, ECS2283, ECS2792, ECS2927, ECS2996, ECS4458, ECS5272, ECS5304, ECS5305, ECSF_3727, ECSF_4152, ECSF2757, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, P423 — 16715c, P423 — 16735c, P423 — 16745c, P423 — 16780c, ECNA114 — 4753, P423 — 10825c, SEQ ID NO: 376, SEQ ID NO: 377, SEQ ID NO: 378, SEQ ID NO: 379, SEQ ID NO: 380, SEQ ID NO: 381, SEQ ID NO: 382, SEQ ID NO: 383, SEQ ID NO: 384, SEQ ID NO: 385, SEQ ID NO: 386, SEQ ID NO: 387, SEQ ID NO: 388, SEQ ID NO: 389, SEQ ID NO: 390, SEQ ID NO: 455, SEQ ID NO: 456, At least four genes selected from the group consisting of finely SEQ ID NO: 461, a method for cloning identification method and / or strain identification of E. coli according to claim 1. The genomic islet in the ORF of (1) is ECNA114 — 4208, EC55989 — 4085, EC55989 — 0018, ECNA114 — 1457, EC55989 — 1089, LF82 — 085, ECS4731, ECS2436, ECNA114 — 0460 and ECS0053, and / or ECNA114 — 4208, EC55989 — 4089, EC55989 — 4089, 10 genes consisting of ECNA114 — 0460 and ECS0053, and the genomic island in the ORF of (2) is ECS1190, Z2415, Z1432, ECS3501, ECH74115 — 1587, EC55989 — 2129, Z1797, EC55989 — 2461, ECH74115 — 2877, ECH74115 — 1791 Or ECNA114 — 0874, EC55989 — 1406, ECNA114 — 2097, EC55989 — 2129, ECNA114 — 3979, ECNA114 — 4026, ECNA114 — 1225, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65 and SEQ ID NO: 66, and / or ECNA114 — 0874, P423 — 10825c, EC55989 — 2126, EC55989 — 2129, EC SEQ ID NO: 63, SEQ ID NO: 376, Column number 380, SEQ ID NO: 381, SEQ ID NO: 389, which is 12 kinds of genes consisting of SEQ ID NO: 390 and SEQ ID NO: 461, clone identification and strain identification methods of E. coli according to claim 1. SEQ ID NO: 1 and 2, SEQ ID NO: 3 and 4, SEQ ID NO: 5 and 6, SEQ ID NO: 7 and 8, SEQ ID NO: 9 and 10, or SEQ ID NO: 413 and 414, SEQ ID NO: 11 and 12, or SEQ ID NO: 415 and 416 , SEQ ID NO: 13 and 14 or SEQ ID NO: 417 and 418, SEQ ID NO: 15 and 16, SEQ ID NO: 17 and 18 or SEQ ID NO: 419 and 420, SEQ ID NO: 19 and 20 or SEQ ID NO: 421 and 422 The above-mentioned (by the above-mentioned base sequence may have addition, substitution, deletion and / or insertion of bases of 2 bases or less) using the PCR method, 1) ORF was detected, and SEQ ID NO: 76 and 77, SEQ ID NO: 78 and 79, SEQ ID NO: 80 and 81, SEQ ID NO: 82 and 83, SEQ ID NO: 84 and 85, SEQ ID NO: 86 and 87, SEQ ID NO: 88 and 9, SEQ ID NO: 90 and 91, SEQ ID NO: 92 and 93, SEQ ID NO: 94 and 95, SEQ ID NO: 96 and 97, SEQ ID NO: 98 and 99, SEQ ID NO: 100 and 101 or SEQ ID NO: 403 and 404, SEQ ID NO: 102 and 103, SEQ ID NO: 104 and 105, SEQ ID NO: 108 and 109, SEQ ID NO: 110 and 111 or SEQ ID NO: 391 and 392, SEQ ID NO: 112 and 113, SEQ ID NO: 114 and 115, SEQ ID NO: 116 and 117, SEQ ID NO: 393 and 394, SEQ ID NO: 395 and 396, SEQ ID Nos. 397 and 398, SEQ ID Nos. 401 and 402, SEQ ID Nos. 405 and 406, SEQ ID Nos. 407 and 408, SEQ ID Nos. 462 and 463, and 30 sets of nucleotide sequences shown in SEQ ID Nos. 464 and 465 Combination (however, the above base sequence has addition, substitution, deletion and / or insertion of 2 or less bases) Using 29 pairs of primers consisting of may also be) you are, the detection of the ORF of the by PCR (2), clone identification method and / or strain of E. coli according to any one of claims 1 4 Method for identification. The clone identification method and / or strain identification method according to claim 5 , wherein the base sequence has no base addition, substitution, deletion and / or insertion. The clone identification method and / or strain identification method according to claim 5 or 6 , wherein the PCR method is a multiplex PCR method. The clone identification method for Escherichia coli according to any one of claims 1 to 7 , wherein the detection result of the presence or absence of ORF in (4) is replaced with 1 (yes) and 0 (no), respectively, and binary coded. And / or methods for strain identification. The clone identification method and / or the strain identification method according to claim 8 , wherein the binary encoding result is further decimal encoded. SEQ ID NO: 1 and 2, SEQ ID NO: 3 and 4, SEQ ID NO: 5 and 6, SEQ ID NO: 7 and 8, SEQ ID NO: 9 and 10, or SEQ ID NO: 413 and 414, SEQ ID NO: 11 and 12, or SEQ ID NO: 415 and 416 , SEQ ID NO: 13 and 14 or SEQ ID NO: 417 and 418, SEQ ID NO: 15 and 16, SEQ ID NO: 17 and 18 or SEQ ID NO: 419 and 420, SEQ ID NO: 19 and 20 or SEQ ID NO: 421 and 422 10 primers consisting of a combination of sequences (however, the above base sequence may have addition, substitution, deletion and / or insertion of 2 or less bases), SEQ ID NO: 76 and 77, sequence Nos. 78 and 79, SEQ ID Nos. 80 and 81, SEQ ID Nos. 82 and 83, SEQ ID Nos. 84 and 85, SEQ ID Nos. 86 and 87, SEQ ID Nos. 88 and 89, SEQ ID Nos. 90 and 91, SEQ ID Nos. 92 and 93 SEQ ID NO: 94 and 95, SEQ ID NO: 96 and 97, SEQ ID NO: 98 and 99, SEQ ID NO: 100 and 101 or SEQ ID NO: 403 and 404, SEQ ID NO: 102 and 103, SEQ ID NO: 104 and 105, SEQ ID NO: 108 and 109, SEQ ID NO: 110 and 111 or SEQ ID NO: 391 and 392, SEQ ID NO: 112 and 113, SEQ ID NO: 114 and 115, SEQ ID NO: 116 and 117, SEQ ID NO: 393 and 394, SEQ ID NO: 395 and 396, SEQ ID NO: 397 and 398, SEQ ID NO: 401 402, SEQ ID NOS: 405 and 406, SEQ ID NOS: 407 and 408, SEQ ID NOS: 462 and 463, and SEQ ID NOS: 464 and 465, which are combinations of 30 base sequences (provided that the base sequence is a base of 2 bases or less) Including 29 sets of primers (which may have additions, substitutions, deletions and / or insertions) Clone identification method and / or primer set for strain identification. The clone identification method of Escherichia coli according to claim 10 and / or a primer set for strain identification, wherein the base sequence has no base addition, substitution, deletion and / or insertion.