Vander Broek Charles W, Stevens Joanne M
The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of EdinburghMidlothian, United Kingdom.
Front Cell Infect Microbiol. 2017 Jun 15;7:255. doi: 10.3389/fcimb.2017.00255. eCollection 2017.
is a Gram-negative intracellular pathogen and the causative agent of melioidosis, a severe disease of both humans and animals. Melioidosis is an emerging disease which is predicted to be vastly under-reported. Type III Secretion Systems (T3SSs) are critical virulence factors in Gram negative pathogens of plants and animals. The genome of encodes three T3SSs. T3SS-1 and -2, of which little is known, are homologous to Hrp2 secretion systems of the plant pathogens and . T3SS-3 is better characterized and is homologous to the Inv/Mxi-Spa secretion systems of spp. and , respectively. Upon entry into the host cell, requires T3SS-3 for efficient escape from the endosome. T3SS-3 is also required for full virulence in both hamster and murine models of infection. The regulatory cascade which controls T3SS-3 expression and the secretome of T3SS-3 have been described, as well as the effect of mutations of some of the structural proteins. Yet only a few effector proteins have been functionally characterized to date and very little work has been carried out to understand the hierarchy of assembly, secretion and temporal regulation of T3SS-3. This review aims to frame current knowledge of T3SSs in the context of other well characterized model T3SSs, particularly those of and .
是一种革兰氏阴性胞内病原体,也是类鼻疽病的病原体,类鼻疽病是一种人和动物都会患的严重疾病。类鼻疽病是一种新发疾病,预计报告率极低。III型分泌系统(T3SSs)是动植物革兰氏阴性病原体中的关键毒力因子。的基因组编码三种T3SSs。人们对T3SS-1和T3SS-2了解甚少,它们与植物病原体和的Hrp2分泌系统同源。T3SS-3的特征更为明确,分别与沙门氏菌属和志贺氏菌属的Inv/Mxi-Spa分泌系统同源。进入宿主细胞后,需要T3SS-3才能有效地从内体中逃逸。在仓鼠和小鼠感染模型中,完全毒力也需要T3SS-3。已经描述了控制T3SS-3表达的调控级联和T3SS-3的分泌蛋白组,以及一些结构蛋白突变的影响。然而,迄今为止,只有少数效应蛋白得到了功能表征,对于理解T3SS-3的组装、分泌和时间调控层次,所做的工作非常少。本综述旨在将目前关于的T3SSs的知识,置于其他特征明确的模型T3SSs的背景下,特别是和的那些T3SSs。