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促进大肠杆菌发病机制的转运蛋白。

Transport proteins promoting Escherichia coli pathogenesis.

机构信息

Department of Molecular Biology, Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116, USA.

出版信息

Microb Pathog. 2014 Jun-Jul;71-72:41-55. doi: 10.1016/j.micpath.2014.03.008. Epub 2014 Apr 18.

Abstract

Escherichia coli is a genetically diverse species infecting hundreds of millions of people worldwide annually. We examined seven well-characterized E. coli pathogens causing urinary tract infections, gastroenteritis, pyelonephritis and haemorrhagic colitis. Their transport proteins were identified and compared with each other and a non-pathogenic E. coli K12 strain to identify transport proteins related to pathogenesis. Each pathogen possesses a unique set of protein secretion systems for export to the cell surface or for injecting effector proteins into host cells. Pathogens have increased numbers of iron siderophore receptors and ABC iron uptake transporters, but the numbers and types of low-affinity secondary iron carriers were uniform in all strains. The presence of outer membrane iron complex receptors and high-affinity ABC iron uptake systems correlated, suggesting co-evolution. Each pathovar encodes a different set of pore-forming toxins and virulence-related outer membrane proteins lacking in K12. Intracellular pathogens proved to have a characteristically distinctive set of nutrient uptake porters, different from those of extracellular pathogens. The results presented in this report provide information about transport systems relevant to various types of E. coli pathogenesis that can be exploited in future basic and applied studies.

摘要

大肠杆菌是一种遗传多样性的物种,每年感染全球数亿人。我们研究了七种特征明确的引起尿路感染、胃肠炎、肾盂肾炎和出血性结肠炎的大肠杆菌病原体。鉴定了它们的转运蛋白,并相互比较,以及与非致病性大肠杆菌 K12 株进行比较,以确定与发病机制相关的转运蛋白。每种病原体都具有独特的蛋白质分泌系统,用于向细胞表面输出或向宿主细胞注射效应蛋白。病原体具有更多的铁载体受体和 ABC 铁摄取转运体,但所有菌株的低亲和力次级铁载体的数量和类型都是一致的。外膜铁复合物受体和高亲和力 ABC 铁摄取系统的存在呈正相关,表明共同进化。每个菌型都编码一组不同的孔形成毒素和缺乏 K12 的与毒力相关的外膜蛋白。细胞内病原体被证明具有一组独特的营养摄取孔道,与细胞外病原体不同。本报告中提出的结果提供了与各种类型大肠杆菌发病机制相关的转运系统信息,可用于未来的基础和应用研究。

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