Campos L C, Whittam T S, Gomes T A, Andrade J R, Trabulsi L R
Departamento de Microbiologia, Universidade de São Paulo, Brazil.
Infect Immun. 1994 Aug;62(8):3282-8. doi: 10.1128/iai.62.8.3282-3288.1994.
Genetic variation among isolates of Escherichia coli O111 obtained mostly from patients with diarrhea in Brazil was assessed by multilocus enzyme electrophoresis to characterize chromosomal genotypes and by gene probes and adherence assays to characterize virulence properties. Among the 152 isolates, we resolved 16 distinct electrophoretic types (ETs), which differed on average at 40% of the enzyme loci. We identified four major bacterial O111 clones of different disease classes: ET 12, which includes the bulk of the enteropathogenic E. coli strains, typically showing localized adherence and intimate attachment in tissue culture assays; ET 1, which includes strains with a different set of virulence markers; ET 9, which includes strains that show intimate attachment but lack localized adherence and Shiga-like toxin genes; and ET 8, which includes strains that are Shiga-like toxin producers and have the corresponding traits of enterohemorrhagic E. coli. Enteroaggregative strains constituted ET 10 and also occurred in ET 1. Isolates of the major clones were found in South and North America and matched in ET and virulence factors to previously described diarrheagenic clones that are widely disseminated in the human population. Because the major clones are genetically distantly related and exhibit different combinations of virulence factors, we hypothesize that they have distinct mechanisms of pathogenesis. The results indicate that genetic divergence of bacteria with the O111 antigen, as measured by allelic variation in enzyme loci, is accompanied by divergence in virulence properties of clones so that identification and classification of pathogenic E. coli strains cannot be based solely on serotyping or a single virulence factor.
通过多位点酶电泳评估主要从巴西腹泻患者中分离出的大肠杆菌O111菌株之间的遗传变异,以表征染色体基因型,并通过基因探针和黏附试验来表征毒力特性。在152株分离菌株中,我们解析出16种不同的电泳类型(ETs),它们在平均40%的酶位点上存在差异。我们鉴定出四种不同疾病类型的主要细菌O111克隆:ET 12,其中包括大部分肠致病性大肠杆菌菌株,在组织培养试验中通常表现出局部黏附和紧密附着;ET 1,其中包括具有不同毒力标记组合的菌株;ET 9,其中包括表现出紧密附着但缺乏局部黏附和志贺样毒素基因的菌株;以及ET 8,其中包括志贺样毒素产生菌且具有肠出血性大肠杆菌相应特征的菌株。肠聚集性菌株构成ET 10,也出现在ET 1中。主要克隆的分离菌株在南美洲和北美洲均有发现,其ET和毒力因子与先前描述的在人群中广泛传播的致泻性克隆相匹配。由于主要克隆在遗传上关系较远且表现出不同的毒力因子组合,我们推测它们具有不同的致病机制。结果表明,通过酶位点的等位基因变异衡量的具有O111抗原的细菌的遗传差异,伴随着克隆毒力特性的差异,因此致病性大肠杆菌菌株的鉴定和分类不能仅基于血清分型或单一毒力因子。