Feng P, Monday S R
Division of Microbiological Studies, US Food and Drug Administration, Washington DC 20204, USA.
Mol Cell Probes. 2000 Dec;14(6):333-7. doi: 10.1006/mcpr.2000.0323.
A multiplex PCR assay was developed which allowed the simultaneous detection of five trait genes or virulence markers in enterohemorrhagic Escherichia coli (EHEC) serotypes. A primer pair, designed to detect a single base-pair mutation in the uidA gene, is specific only for the prototypic EHEC of O157:H7 serotype and its toxigenic, non-motile variants. In a similar way, primers to the eaeA gene of the gamma-intimin derivative specifically detects strains in the EHEC 1 clonal group, which consists mostly of O157:H7 and some O55:H7 serotypes. The other three primer pairs, specific for stx1, stx2 and both variants of ehxA genes, will detect the presence of these virulence genes in all EHEC serotypes. Analysis of 34 strains, including various serotypes of EHEC, Shiga toxin-producing E. coli and enteropathogenic E. coli, confirmed that the multiplex PCR assay detected the presence of these genes in a manner consistent with the known genotype of each respective strains.
开发了一种多重聚合酶链反应(PCR)检测方法,可同时检测肠出血性大肠杆菌(EHEC)血清型中的五个性状基因或毒力标记。一对引物被设计用于检测uidA基因中的单碱基对突变,该引物仅对O157:H7血清型的原型EHEC及其产毒、无动力变体具有特异性。同样,针对γ-紧密素衍生物的eaeA基因的引物可特异性检测EHEC 1克隆群中的菌株,该克隆群主要由O157:H7和一些O55:H7血清型组成。另外三对引物分别针对stx1、stx2和ehxA基因的两种变体,可检测所有EHEC血清型中这些毒力基因的存在。对34株菌株进行分析,包括各种血清型的EHEC、产志贺毒素大肠杆菌和肠致病性大肠杆菌,证实多重PCR检测方法检测这些基因的方式与各菌株已知基因型一致。