Kudva I T, Hatfield P G, Hovde C J
Department of Microbiology, Molecular Biology, and Biochemistry University of Idaho, Moscow 83843, USA.
J Clin Microbiol. 1997 Apr;35(4):892-9. doi: 10.1128/jcm.35.4.892-899.1997.
The isolation and characterization of Escherichia coli O157:H7 and non-O157 Shiga toxin-producing E. coli (STEC) strains from sheep are described. One flock was investigated for E. coli O157:H7 over a 16-month period that spanned two summer and two autumn seasons. Variation in the occurrence of E. coli O157:H7-positive sheep was observed, with animals being culture positive only in the summer months but not in the spring, autumn, or winter. E. coli O157:H7 isolates were distinguished by pulsed-field gel electrophoresis (PFGE) of chromosomal DNA and toxin gene restriction fragment length polymorphism (RFLP) analysis. Ten PFGE patterns and five RFLP patterns, identified among the isolates, showed that multiple E. coli O157:H7 strains were isolated from one flock, that a single animal simultaneously shed multiple E. coli O157:H7 strains, and that the strains shed by individuals changed over time. E. coli O157:H7 was isolated only by selective enrichment culture off 10 g of ovine feces. In contrast, strains of eight STEC serotypes other than O157:H7 were cultured from feces of sheep from a separate flock without enrichment. The predominant non-O157 STEC serotype found was O91:NM (NM indicates nonmotile), and others included O128:NM, O88:NM, O6:H49, and O5:NM. Irrespective of serotype, 98% of the ovine STEC isolates possessed various combinations of the virulence-associated genes for Shiga toxin(s) and the attaching-and-effacing lesion (stx1, stx2, and eae), suggesting their potential for human pathogenicity. The most common toxin-eae genotype was positive for stx1, stx2, and eae. A Vero cell cytotoxicity assay demonstrated that 90% of the representative STEC isolates tested expressed the toxin gene. The report demonstrates that sheep transiently shed a variety of STEC strains, including E. coli O157:H7, that have potential as human pathogens.
本文描述了从绵羊中分离和鉴定大肠杆菌O157:H7及非O157产志贺毒素大肠杆菌(STEC)菌株的过程。对一个羊群进行了为期16个月的大肠杆菌O157:H7调查,该时间段跨越两个夏季和两个秋季。观察到大肠杆菌O157:H7阳性绵羊的出现存在差异,动物仅在夏季月份培养呈阳性,而在春季、秋季或冬季则不然。通过染色体DNA的脉冲场凝胶电泳(PFGE)和毒素基因限制性片段长度多态性(RFLP)分析对大肠杆菌O157:H7分离株进行了区分。在分离株中鉴定出10种PFGE模式和5种RFLP模式,表明从一个羊群中分离出了多种大肠杆菌O157:H7菌株,一只动物同时排出多种大肠杆菌O157:H7菌株,并且个体排出的菌株随时间变化。仅通过对10克羊粪便进行选择性富集培养才分离出大肠杆菌O157:H7。相比之下,从另一个羊群的绵羊粪便中未经富集培养出了除O157:H7之外的8种STEC血清型的菌株。发现的主要非O157 STEC血清型是O91:NM(NM表示无动力),其他包括O128:NM、O88:NM、O6:H49和O5:NM。无论血清型如何,98%的绵羊STEC分离株都具有志贺毒素和紧密黏附损伤的毒力相关基因(stx1、stx2和eae)的各种组合,表明它们具有人类致病性的潜力。最常见的毒素-eae基因型对stx1、stx2和eae呈阳性。Vero细胞细胞毒性试验表明,90%的代表性STEC分离株检测到表达毒素基因。该报告表明,绵羊会短暂排出多种具有人类致病潜力的STEC菌株,包括大肠杆菌O157:H7。