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铜绿假单胞菌Ⅲ型分泌系统的转录调控

Transcriptional regulation of the Pseudomonas aeruginosa type III secretion system.

作者信息

Yahr Timothy L, Wolfgang Matthew C

机构信息

University of Iowa, Department of Microbiology, Iowa City, IA, USA.

出版信息

Mol Microbiol. 2006 Nov;62(3):631-40. doi: 10.1111/j.1365-2958.2006.05412.x. Epub 2006 Sep 21.

Abstract

Type III secretion systems (T3SS) function by translocating effector proteins into eukaryotic host cells and are important for the virulence of many Gram-negative bacterial pathogens. Although the secretion and translocation machineries are highly conserved between different species, each pathogen translocates a unique set of effectors that subvert normal host cell physiology to promote pathogenesis. The uniqueness of each pathogen is further reflected in the diversity of mechanisms used to regulate T3SS gene expression. Pseudomonas aeruginosa utilizes a complex set of signalling pathways to modulate T3SS expression in response to extracellular and intracellular cues. Whereas some pathways are dedicated solely to regulating the T3SS, others co-ordinately regulate expression of the T3SS with multiple virulence functions on a global scale. Emerging regulatory themes include coupling of T3SS transcription with type III secretory activity, global regulatory control through modulation of cAMP biosynthesis, repression by a variety of stresses, involvement of multiple two component regulatory systems, and an inverse relationship between T3SS expression and multicellular behaviour. Factors controlling activation of T3SS expression likely contribute to the environmental survival of the organism and to the pathogenesis of acute P. aeruginosa infections. Conversely, active repression of the T3SS might contribute to the persistence of chronic infections.

摘要

III型分泌系统(T3SS)通过将效应蛋白转运到真核宿主细胞中发挥作用,对许多革兰氏阴性细菌病原体的毒力至关重要。尽管不同物种之间的分泌和转运机制高度保守,但每种病原体转运的效应蛋白组合都是独特的,这些效应蛋白会破坏正常的宿主细胞生理功能以促进发病机制。每种病原体的独特性还进一步体现在用于调节T3SS基因表达的机制的多样性上。铜绿假单胞菌利用一套复杂的信号通路来响应细胞外和细胞内信号调节T3SS表达。虽然有些通路专门用于调节T3SS,但其他通路则在全局范围内协调调节T3SS与多种毒力功能的表达。新出现的调节主题包括T3SS转录与III型分泌活性的耦合、通过调节cAMP生物合成进行全局调节控制、多种应激的抑制作用、多个双组分调节系统的参与以及T3SS表达与多细胞行为之间的反比关系。控制T3SS表达激活的因素可能有助于该生物体在环境中的生存以及急性铜绿假单胞菌感染的发病机制。相反,T3SS的主动抑制可能有助于慢性感染的持续存在。

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