Beutin Lothar, Kaulfuss Stefan, Herold Sylvia, Oswald Eric, Schmidt Herbert
Division of Microbial Toxins, Department of Biological Safety, Robert Koch Institute, Berlin, Germany.
J Clin Microbiol. 2005 Apr;43(4):1552-63. doi: 10.1128/JCM.43.4.1552-1563.2005.
We investigated the genetic relationships of 54 Escherichia coli O103 strains from humans, animals, and meat by molecular typing of housekeeping and virulence genes and by pulsed-field gel electrophoresis (PFGE). Multilocus sequence typing (MLST) of seven housekeeping genes revealed seven profiles, I through VII. MLST profiles I plus III cover 45 Shiga toxin-producing E. coli (STEC) O103:H2 strains from Australia, Canada, France, Germany, and Northern Ireland that are characterized by the intimin (eae) epsilon gene and carry enterohemorrhagic E. coli (EHEC) virulence plasmids. MLST profile II groups five human and animal enteropathogenic E. coli (EPEC) O103:H2 strains that were positive for intimin (eae) beta. Although strains belonging to MLST groups II and I plus III are closely related to each other (92.6% identity), major differences were found in the housekeeping icdA gene and in the virulence-associated genes eae and escD. E. coli O103 strains with MLST patterns IV to VII are genetically distant from MLST I, II, and III strains, as are the non-O103 E. coli strains EDL933 (O157), MG1655 (K-12), and CFT073 (O6). Comparison of MLST results with those of PFGE and virulence typing demonstrated that E. coli O103 STEC and EPEC have recently acquired different virulence genes and DNA rearrangements, causing alterations in their PFGE patterns. PFGE typing was very useful for identification of genetically closely related subgroups among MLST I strains, such as Stx2-producing STEC O103 strains from patients with hemolytic uremic syndrome. Analysis of virulence genes contributed to grouping of E. coli O103 strains into EPEC and STEC. Novel virulence markers, such as efa (EHEC factor for adherence), paa (porcine adherence factor), and cif (cell cycle-inhibiting factor), were found widely associated with E. coli O103 EPEC and STEC strains.
我们通过管家基因和毒力基因的分子分型以及脉冲场凝胶电泳(PFGE),研究了来自人类、动物和肉类的54株大肠杆菌O103菌株的遗传关系。对7个管家基因进行多位点序列分型(MLST),揭示了7种谱型,即I至VII型。MLST谱型I和III涵盖了来自澳大利亚、加拿大、法国、德国和北爱尔兰的45株产志贺毒素大肠杆菌(STEC)O103:H2菌株,这些菌株以紧密黏附素(eae)ε基因特征,并携带肠出血性大肠杆菌(EHEC)毒力质粒。MLST谱型II将5株人源和动物源肠致病性大肠杆菌(EPEC)O103:H2菌株归为一组,这些菌株的紧密黏附素(eae)β呈阳性。尽管属于MLST II组和I + III组的菌株彼此密切相关(同一性为92.6%),但在管家基因icdA以及与毒力相关的基因eae和escD中发现了主要差异。具有MLST模式IV至VII的大肠杆菌O103菌株在遗传上与MLST I、II和III菌株相距较远,非O103大肠杆菌菌株EDL933(O157)、MG1655(K - 12)和CFT073(O6)也是如此。将MLST结果与PFGE和毒力分型结果进行比较表明,大肠杆菌O103 STEC和EPEC最近获得了不同的毒力基因和DNA重排,导致其PFGE模式发生改变。PFGE分型对于鉴定MLST I菌株中遗传关系密切的亚组非常有用,例如溶血尿毒综合征患者中产stx2的STEC O103菌株。毒力基因分析有助于将大肠杆菌O103菌株分为EPEC和STEC。发现新型毒力标记,如efa(EHEC黏附因子)、paa(猪黏附因子)和cif(细胞周期抑制因子),与大肠杆菌O103 EPEC和STEC菌株广泛相关。