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本文引用的文献

1
Biogenesis of F7 and F7 fimbriae of uropathogenic Escherichia coli: influence of the FsoF and FstFG proteins and localization of the Fso/FstE protein.尿路致病性大肠杆菌F7和F7菌毛的生物合成:FsoF和FstFG蛋白的影响以及Fso/FstE蛋白的定位
Mol Microbiol. 1988 Jan;2(1):73-80. doi: 10.1111/j.1365-2958.1988.tb00008.x.
2
Cooperation of Adhesin Alleles in -Host Tropism.粘附素等位基因在宿主嗜性中的协同作用。
mSphere. 2017 Mar 8;2(2). doi: 10.1128/mSphere.00066-17. eCollection 2017 Mar-Apr.
3
Inflammation-Induced Adhesin-Receptor Interaction Provides a Fitness Advantage to Uropathogenic E. coli during Chronic Infection.炎症诱导的黏附素-受体相互作用为慢性感染期间的尿路致病性大肠杆菌提供了适应性优势。
Cell Host Microbe. 2016 Oct 12;20(4):482-492. doi: 10.1016/j.chom.2016.08.013. Epub 2016 Sep 22.
4
Uropathogenic E. coli Exploit CEA to Promote Colonization of the Urogenital Tract Mucosa.尿路致病性大肠杆菌利用癌胚抗原促进泌尿生殖道黏膜的定植。
PLoS Pathog. 2016 May 12;12(5):e1005608. doi: 10.1371/journal.ppat.1005608. eCollection 2016 May.
5
The UbiI (VisC) Aerobic Ubiquinone Synthase Is Required for Expression of Type 1 Pili, Biofilm Formation, and Pathogenesis in Uropathogenic Escherichia coli.尿路致病性大肠杆菌中1型菌毛的表达、生物膜形成和致病作用需要泛醌I(VisC)需氧泛醌合酶。
J Bacteriol. 2016 Sep 9;198(19):2662-72. doi: 10.1128/JB.00030-16. Print 2016 Oct 1.
6
Catch-bond mechanism of the bacterial adhesin FimH.细菌粘附素FimH的捕获-结合机制。
Nat Commun. 2016 Mar 7;7:10738. doi: 10.1038/ncomms10738.
7
Nitazoxanide Inhibits Pilus Biogenesis by Interfering with Folding of the Usher Protein in the Outer Membrane.硝唑尼特通过干扰外膜中 usher 蛋白的折叠来抑制菌毛生物合成。
Antimicrob Agents Chemother. 2016 Mar 25;60(4):2028-38. doi: 10.1128/AAC.02221-15. Print 2016 Apr.
8
How type 1 fimbriae help Escherichia coli to evade extracellular antibiotics.1型菌毛如何帮助大肠杆菌逃避细胞外抗生素。
Sci Rep. 2016 Jan 5;6:18109. doi: 10.1038/srep18109.
9
Structure of a Chaperone-Usher Pilus Reveals the Molecular Basis of Rod Uncoiling.伴侣-usher菌毛的结构揭示了杆状结构展开的分子基础。
Cell. 2016 Jan 14;164(1-2):269-278. doi: 10.1016/j.cell.2015.11.049. Epub 2015 Dec 24.
10
Dual ligand/receptor interactions activate urothelial defenses against uropathogenic E. coli.双配体/受体相互作用激活尿路上皮对尿路致病性大肠杆菌的防御。
Sci Rep. 2015 Nov 9;5:16234. doi: 10.1038/srep16234.

通过伴侣蛋白/外膜蛋白途径在……和……中组装的菌毛

Pili Assembled by the Chaperone/Usher Pathway in and .

作者信息

Werneburg Glenn T, Thanassi David G

机构信息

Department of Molecular Genetics and Microbiology.

出版信息

EcoSal Plus. 2018 Mar;8(1). doi: 10.1128/ecosalplus.ESP-0007-2017.

DOI:10.1128/ecosalplus.ESP-0007-2017
PMID:29536829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5940347/
Abstract

Gram-negative bacteria assemble a variety of surface structures, including the hair-like organelles known as pili or fimbriae. Pili typically function in adhesion and mediate interactions with various surfaces, with other bacteria, and with other types of cells such as host cells. The chaperone/usher (CU) pathway assembles a widespread class of adhesive and virulence-associated pili. Pilus biogenesis by the CU pathway requires a dedicated periplasmic chaperone and integral outer membrane protein termed the usher, which forms a multifunctional assembly and secretion platform. This review addresses the molecular and biochemical aspects of the CU pathway in detail, focusing on the type 1 and P pili expressed by uropathogenic as model systems. We provide an overview of representative CU pili expressed by and , and conclude with a discussion of potential approaches to develop antivirulence therapeutics that interfere with pilus assembly or function.

摘要

革兰氏阴性菌会组装多种表面结构,包括被称为菌毛或纤毛的毛发状细胞器。菌毛通常在黏附中发挥作用,并介导与各种表面、其他细菌以及与其他类型细胞(如宿主细胞)的相互作用。伴侣/外膜蛋白途径(chaperone/usher,CU)组装了一类广泛存在的与黏附及毒力相关的菌毛。通过CU途径进行菌毛生物合成需要一种专门的周质伴侣蛋白和一种被称为外膜蛋白的整合外膜蛋白,后者形成一个多功能的组装和分泌平台。本综述详细阐述了CU途径的分子和生化方面,重点关注尿路致病性大肠杆菌表达的1型菌毛和P菌毛作为模型系统。我们概述了大肠杆菌和肺炎克雷伯菌表达的代表性CU菌毛,并以讨论开发干扰菌毛组装或功能的抗毒力疗法的潜在方法作为结尾。