Escherichia coli O-Genotyping PCR: a Comprehensive and Practical Platform for Molecular O Serogrouping
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- Atsushi Iguchi
- Department of Animal and Grassland Sciences, Faculty of Agriculture, University of Miyazaki, Miyazaki, Japan
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- Sunao Iyoda
- Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan
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- Kazuko Seto
- Division of Bacteriology, Osaka Prefectural Institute of Public Health, Osaka, Japan
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- Tomoko Morita-Ishihara
- Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan
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- Flemming Scheutz
- Department of Microbiology Infection Control, Statens Serum Institut, Copenhagen, Denmark
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- Makoto Ohnishi
- Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan
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- P. Bourbeau
- editor
書誌事項
- 公開日
- 2015-08
- 権利情報
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- https://journals.asm.org/non-commercial-tdm-license
- DOI
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- 10.1128/jcm.00321-15
- 公開者
- American Society for Microbiology
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説明
<jats:title>ABSTRACT</jats:title> <jats:p> The O serogrouping of pathogenic <jats:named-content content-type="genus-species">Escherichia coli</jats:named-content> is a standard method for subtyping strains for epidemiological studies and enhancing phylogenetic studies. In particular, the identification of strains of the same O serogroup is essential in outbreak investigations and surveillance. In a previous study, we analyzed the O-antigen biosynthesis gene cluster in all known <jats:named-content content-type="genus-species">E. coli</jats:named-content> O serogroups (A. Iguchi et al., DNA Res, 22:101–107, 2015, <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://dx.doi.org/10.1093/dnares/dsu043">http://dx.doi.org/10.1093/dnares/dsu043</jats:ext-link> ). Based on those results, we have arranged 162 PCR primer pairs for the identification or classification of O serogroups. Of these, 147 pairs were used to identify 147 individual O serogroups with unique O-antigen biosynthesis genes, and the other 15 pairs were used to identify 15 groups of strains (Gp1 to Gp15). Each of these groups consisted of strains with identical or very similar O-antigen biosynthesis genes, and the groups represented a total of 35 individual O serogroups. We then used the 162 primer pairs to create 20 multiplex PCR sets. Each set contained six to nine primer pairs that amplify products of markedly different sizes. This genetic methodology ( <jats:named-content content-type="genus-species">E. coli</jats:named-content> O-genotyping PCR) allowed for comprehensive, rapid, and low-cost typing. Validation of the PCR system using O-serogroup references and wild strains showed that the correct O serogroups were specifically and accurately identified for 100% (182/182) and 90.8% (522/575) of references and wild strains, respectively. The PCR-based system reported here might be a promising tool for the subtyping of <jats:named-content content-type="genus-species">E. coli</jats:named-content> strains for epidemiological studies as well as for the surveillance of pathogenic <jats:named-content content-type="genus-species">E. coli</jats:named-content> during outbreaks. </jats:p>
収録刊行物
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- Journal of Clinical Microbiology
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Journal of Clinical Microbiology 53 (8), 2427-2432, 2015-08
American Society for Microbiology