4.5 Article

A complete view of the genetic diversity of the Escherichia coli O-antigen biosynthesis gene cluster

Journal

DNA RESEARCH
Volume 22, Issue 1, Pages 101-107

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/dnares/dsu043

Keywords

E. coli; O-antigen biosynthesis gene cluster; horizontal gene transfer; O serogroup; genomic diversity

Funding

  1. Health Labor Sciences Research Grants from the Ministry of Health, Labor, and Welfare, Japan [H25-Syokuhin-Wakate-018, H24-Shinkou-Ippan-012]
  2. Adaptable and Seamless Technology Transfer Program through Target-driven R&D from Japan Science and Technology Agency [AS242Z00217P]
  3. Scientific Research Grant on Priority Areas from the University of Miyazaki
  4. Program to Disseminate Tenure Tracking System from the Japanese Ministry of Education, Culture, Sports, Science, and Technology
  5. Wellcome Trust grant [098051]
  6. University of Miyazaki, Japan
  7. Grants-in-Aid for Scientific Research [24780044, 25460542] Funding Source: KAKEN

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The O antigen constitutes the outermost part of the lipopolysaccharide layer in Gram-negative bacteria. The chemical composition and structure of the O antigen show high levels of variation even within a single species revealing itself as serological diversity. Here, we present a complete sequence set for the O-antigen biosynthesis gene clusters (O-AGCs) from all 184 recognized Escherichia coli O serogroups. By comparing these sequences, we identified 161 well-defined O-AGCs. Based on the wzx/wzy or wzm/wzt gene sequences, in addition to 145 singletons, 37 serogroups were placed into 16 groups. Furthermore, phylogenetic analysis of all the E. coli O-serogroup reference strains revealed that the nearly one-quarter of the 184 serogroups were found in the ST10 lineage, which may have a unique genetic background allowing a more successful exchange of O-AGCs. Our data provide a complete view of the genetic diversity of O-AGCs in E. coli showing a stronger association between host phylogenetic lineage and O-serogroup diversification than previously recognized. These data will be a valuable basis for developing a systematic molecular O-typing scheme that will allow traditional typing approaches to be linked to genomic exploration of E. coli diversity.

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