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尿路致病性大肠杆菌的F9菌毛在生物膜形成中的作用。

The role of F9 fimbriae of uropathogenic Escherichia coli in biofilm formation.

作者信息

Ulett Glen C, Mabbett Amanda N, Fung Khe C, Webb Richard I, Schembri Mark A

机构信息

School of Molecular and Microbial Sciences, University of Queensland, Brisbane, Queensland 4072, Australia.

Centre for Microscopy and Microanalysis, University of Queensland, Brisbane, Queensland 4072, Australia.

出版信息

Microbiology (Reading). 2007 Jul;153(Pt 7):2321-2331. doi: 10.1099/mic.0.2006/004648-0.

Abstract

Uropathogenic Escherichia coli (UPEC) is the primary cause of urinary tract infection (UTI) in the developed world. The major factors associated with virulence of UPEC are fimbrial adhesins, which mediate attachment to specific receptors, enhance persistence and trigger innate host responses. UPEC produce a range of fimbrial adhesins, with type 1 and P fimbriae of the chaperone-usher subclass being the best characterized. The prototype UPEC strain CFT073 contains ten gene clusters that contain genes characteristic of this class of fimbriae. However, only five of these gene clusters have been characterized in detail. In this study the F9 fimbrial gene cluster (c1931-c1936) from CFT073 has been characterized. The F9 fimbriae-encoding genes were PCR amplified, cloned and expressed in a K-12 background devoid of type 1 fimbriae. While F9 fimbrial expression was not associated with any haemagglutination or cellular adherence properties, a role in biofilm formation was observed. E. coli K-12 cells expressing F9 fimbriae produced a dense and uniform biofilm in both microtitre plate and continuous-flow biofilm model systems. In wild-type UPEC CFT073, expression of the F9 major subunit-encoding gene was detected during exponential growth in M9 minimal medium. F9 expression could also be detected following selection and enrichment for pellicle growth in a CFT073fim foc double mutant. The F9 genes appear to be common in UPEC and other types of pathogenic E. coli. However, their precise contribution to disease remains to be determined.

摘要

致病性大肠杆菌(UPEC)是发达国家尿路感染(UTI)的主要病因。与UPEC毒力相关的主要因素是菌毛黏附素,它介导与特定受体的结合,增强持久性并触发宿主固有免疫反应。UPEC产生一系列菌毛黏附素,伴侣-usher亚类的1型菌毛和P菌毛的特征最为明显。UPEC原型菌株CFT073包含十个基因簇,这些基因簇含有此类菌毛的特征性基因。然而,这些基因簇中只有五个已被详细鉴定。在本研究中,对来自CFT073的F9菌毛基因簇(c1931-c1936)进行了鉴定。对编码F9菌毛的基因进行PCR扩增、克隆,并在不含1型菌毛的K-12背景中表达。虽然F9菌毛的表达与任何血凝或细胞黏附特性无关,但观察到其在生物膜形成中发挥作用。表达F9菌毛的大肠杆菌K-12细胞在微量滴定板和连续流生物膜模型系统中均产生了致密且均匀的生物膜。在野生型UPEC CFT073中,在M9基本培养基中指数生长期间检测到了F9主要亚基编码基因的表达。在CFT073fim foc双突变体中选择并富集形成菌膜生长后,也能检测到F9的表达。F9基因似乎在UPEC和其他类型的致病性大肠杆菌中很常见。然而,它们对疾病的确切作用仍有待确定。

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