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比较分析来自人类、动物和环境源的产志贺毒素 2g 和耐热肠毒素 STIa 编码大肠杆菌分离株的毒力基因、遗传多样性和系统发育。

Comparative analysis of virulence genes, genetic diversity, and phylogeny of Shiga toxin 2g and heat-stable enterotoxin STIa encoding Escherichia coli isolates from humans, animals, and environmental sources.

机构信息

Robert Koch-Institute, Wernigerode Branch, Burgstr. 37, 38855 Wernigerode, Germany.

出版信息

Int J Med Microbiol. 2011 Mar;301(3):181-91. doi: 10.1016/j.ijmm.2010.06.003. Epub 2010 Aug 21.

DOI:10.1016/j.ijmm.2010.06.003
PMID:20728406
Abstract

An analysis for stx(2) variants among the 2010 human stx(2)-positive Shiga toxin-producing Escherichia coli (STEC) strains from Germany collected at the National Reference Centre 1999-2008 revealed 0.6% to possess the recently described stx(2g) gene. Sequencing of the whole stx(2g) operons showed new alleles and pseudogenes. The further molecular, phenotypic, and phylogenetic comparison of 12 human stx(2g)-harbouring isolates with 12 stx(2g)-harbouring isolates from animals or environmental sources demonstrated that both groups are closely related, indicating the human infections as a potential zoonotic disease. Although originating from various different sources, the stx(2g)-containing strains belong to only 3 phylogenetic lineages, represented by 4 serovars belonging to 4 sequence types. In view of the huge diversity among other STEC, this suggests the emergence of the stx(2g) variant as a rather recent microevolutionary event. Interestingly, in the strains under investigation, Stx2g was not expressed. However, all of them contained the estIa gene which typically is associated with enterotoxin-producing E. coli and did express STIa. By this combination of virulence genes of different pathotypes of intestinal pathogenic E. coli, these strains represent a new, intermediate pathotype and emerging pathogens. Given a rising number of intermediate pathotypes becoming described among E. coli, a wider range of virulence markers should be included in the regular pathotype diagnostics.

摘要

对 1999 年至 2008 年期间在德国国家参考中心收集的 2010 株人源 stx(2)阳性产志贺毒素大肠杆菌(STEC)菌株中 stx(2)变异株的分析表明,有 0.6%的菌株携带最近描述的 stx(2g)基因。stx(2g)全操纵子的测序显示了新的等位基因和假基因。对 12 株人源 stx(2g)携带株与 12 株动物或环境来源的 stx(2g)携带株的进一步分子、表型和系统发育比较表明,这两组密切相关,表明人类感染可能是一种人畜共患病。尽管源自不同的来源,但含有 stx(2g)的菌株仅属于 3 个系统发育谱系,由属于 4 个序列类型的 4 个血清型代表。鉴于其他 STEC 的巨大多样性,这表明 stx(2g)变异株的出现是一个相当新的微进化事件。有趣的是,在所研究的菌株中,Stx2g 未表达。然而,它们都含有 estIa 基因,该基因通常与产肠毒素大肠杆菌相关,并且确实表达了 STIa。通过不同肠致病性大肠杆菌不同病原型的毒力基因的这种组合,这些菌株代表了一种新的、中间病原型和新兴的病原体。鉴于越来越多的中间病原型在大肠杆菌中被描述,应该在常规病原型诊断中纳入更广泛的毒力标志物。

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