首页> 美国卫生研究院文献>Journal of Bacteriology >Escherichia coli Serotype O55:H7 Diversity Supports Parallel Acquisition of Bacteriophage at Shiga Toxin Phage Insertion Sites during Evolution of the O157:H7 Lineage
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Escherichia coli Serotype O55:H7 Diversity Supports Parallel Acquisition of Bacteriophage at Shiga Toxin Phage Insertion Sites during Evolution of the O157:H7 Lineage

机译:大肠杆菌O55:H7血清型多样性支持O157:H7谱系进化过程中志贺毒素噬菌体插入位点噬菌体的并行获取

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摘要

Enteropathogenic Escherichia coli (EPEC) continues to be a leading cause of mortality and morbidity in children around the world. Two EPEC genomes have been fully sequenced: those of EPEC O127:H6 strain E2348/69 (United Kingdom, 1969) and EPEC O55:H7 strain CB9615 (Germany, 2003). The O55:H7 serotype is a recent precursor to the virulent enterohemorrhagic E. coli O157:H7. To explore the diversity of O55:H7 and better understand the clonal evolution of O157:H7, we fully sequenced EPEC O55:H7 strain RM12579 (California, 1974), which was collected 1 year before the first U.S. isolate of O157:H7 was identified in California. Phage-related sequences accounted for nearly all differences between the two O55:H7 strains. Additionally, O55:H7 and O157:H7 strains were tested for the presence and insertion sites of Shiga toxin gene (stx)-containing bacteriophages. Analysis of non-phage-associated genes supported core elements of previous O157:H7 stepwise evolutionary models, whereas phage composition and insertion analyses suggested a key refinement. Specifically, the placement and presence of lambda-like bacteriophages (including those containing stx) should not be considered stable evolutionary markers or be required in placing O55:H7 and O157:H7 strains within the stepwise evolutionary models. Additionally, we suggest that a 10.9-kb region (block 172) previously believed unique to O55:H7 strains can be used to identify early O157:H7 strains. Finally, we defined two subsets of O55:H7 strains that share an as-yet-unobserved or extinct common ancestor with O157:H7 strains. Exploration of O55:H7 diversity improved our understanding of the evolution of E. coli O157:H7 and suggested a key revision to accommodate existing and future configurations of stx-containing bacteriophages into current models.
机译:肠致病性大肠杆菌(EPEC)仍然是世界各地儿童死亡率和发病率的主要原因。已经对两个EPEC基因组进行了完整测序:EPEC O127:H6株E2348 / 69(英国,1969年)和EPEC O55:H7株CB9615(德国,2003年)。 O55:H7血清型是剧毒肠出血性大肠杆菌O157:H7的最新先兆。为了探索O55:H7的多样性并更好地了解O157:H7的克隆进化,我们对EPEC O55:H7菌株RM12579(加利福尼亚,1974)进行了完整测序,该菌株在鉴定出第一个美国O157:H7分离株之前一年收集在加利福尼亚。噬菌体相关的序列几乎解释了两个O55:H7菌株之间的所有差异。此外,测试了O55:H7和O157:H7菌株是否含有志贺毒素基因(stx)噬菌体和其插入位点。非噬菌体相关基因的分析支持以前的O157:H7逐步进化模型的核心元素,而噬菌体组成和插入分析则提出了一个关键的改进。具体而言,λ型噬菌体(包括含有stx的噬菌体)的放置和存在不应被视为稳定的进化标记,也不应该在逐步进化模型中放置O55:H7和O157:H7菌株时需要。此外,我们建议可以使用以前认为是O55:H7株特有的10.9-kb区域(框172)来鉴定早期的O157:H7株。最后,我们定义了O55:H7菌株的两个子集,它们与O157:H7菌株具有尚未观察到或已灭绝的共同祖先。对O55:H7多样性的探索提高了我们对大肠杆菌O157:H7进化的理解,并建议进行关键修订,以将含stx的噬菌体的现有和未来配置纳入当前模型。

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