Iguchi Atsushi, Iyoda Sunao, Kikuchi Taisei, Ogura Yoshitoshi, Katsura Keisuke, Ohnishi Makoto, Hayashi Tetsuya, Thomson Nicholas R
Department of Animal and Grassland Sciences, Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Japan
Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
DNA Res. 2015 Feb;22(1):101-7. doi: 10.1093/dnares/dsu043. Epub 2014 Nov 26.
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.
O抗原构成革兰氏阴性菌脂多糖层的最外层。即使在单个物种内,O抗原的化学成分和结构也表现出高度的变异性,呈现出血清学多样性。在此,我们展示了来自所有184个已确认的大肠杆菌O血清群的O抗原生物合成基因簇(O-AGCs)的完整序列集。通过比较这些序列,我们鉴定出161个明确的O-AGCs。基于wzx/wzy或wzm/wzt基因序列,除了145个单一组外,37个血清群被归入16个组。此外,对所有大肠杆菌O血清群参考菌株的系统发育分析表明,在184个血清群中,近四分之一存在于ST10谱系中,这可能具有独特的遗传背景,使得O-AGCs的交换更为成功。我们的数据提供了大肠杆菌中O-AGCs遗传多样性的完整视图,显示出宿主系统发育谱系与O血清群多样化之间的关联比之前认识到的更强。这些数据将成为开发系统分子O分型方案(该方案将使传统分型方法与大肠杆菌多样性的基因组探索相联系)的宝贵基础。