International Course of Agriculture, Graduate School of Agriculture, University of Miyazaki, Miyazaki, Japan.
Department of Animal and Grassland Sciences, Faculty of Agriculture, University of Miyazaki, Miyazaki, Japan
J Clin Microbiol. 2018 May 25;56(6). doi: 10.1128/JCM.00190-18. Print 2018 Jun.
In , more than 180 O groups and 53 H types have been recognized. The O:H serotyping of strains is an effective method for identifying strains with pathogenic potential and classifying them into clonal groups. In particular, the serotyping of Shiga toxin-producing (STEC) strains provides valuable information to evaluate the routes, sources, and prevalence of agents in outbreak investigations and surveillance. Here, we present a complete and practical PCR-based H-typing system, H-genotyping PCR, consisting of 10 multiplex PCR kits with 51 single PCR primer pairs. Primers were designed based on a detailed comparative analysis of sequences from all H-antigen (flagellin)-encoding genes, and its homologs. The specificity of this system was confirmed by using all H type reference strains. Additionally, 362 serotyped wild strains were also used to evaluate its practicality. All 277 H-type-identified isolates gave PCR products that corresponded to the results of serological H typing. Moreover, 76 nonmotile and nine untypeable strains could be successfully subtyped into any H type by the PCR system. The H-genotyping PCR developed here allows broader, rapid, and low-cost subtyping of H types and will assist epidemiological studies as well as surveillance of pathogenic .
在 中,已经识别出超过 180 个 O 群和 53 个 H 型。菌株的 O:H 血清型分型是识别具有致病潜力的菌株并将其分类为克隆群的有效方法。特别是产志贺毒素的 (STEC) 菌株的血清分型为评估暴发调查和监测中病原体的途径、来源和流行情况提供了有价值的信息。在这里,我们提出了一种完整实用的基于 PCR 的 H 型分型系统,H 基因分型 PCR,由 10 个多重 PCR 试剂盒和 51 对单 PCR 引物组成。引物是基于对所有 H 抗原(鞭毛)编码基因及其同源物的序列进行详细比较分析而设计的。该系统的特异性通过使用所有 H 型参考菌株得到了证实。此外,还使用了 362 种定型的野生菌株来评估其实用性。所有 277 种 H 型鉴定分离株的 PCR 产物均与血清学 H 型分型结果相对应。此外,76 株非动力和 9 株不可分型的菌株可通过 PCR 系统成功分为任何 H 型。这里开发的 H 基因分型 PCR 允许更广泛、快速和低成本的 H 型分型,并将有助于流行病学研究以及对致病性 的监测。