Centre for Molecular Microbiology and Infection, Department of Life Sciences, Imperial College, London, UK.
Department of Molecular Evolution, Centro de Astrobiología, Instituto Nacional de Técnica Aeroespacial-Consejo Superior de Investigaciones Científicas (INTA-CSIC), Madrid, Spain.
Trends Microbiol. 2022 Jun;30(6):524-533. doi: 10.1016/j.tim.2021.10.007. Epub 2021 Nov 25.
Type III secretion system (T3SS) effectors are key virulence factors that underpin the infection strategy of many clinically important Gram-negative pathogens, including Salmonella enterica, Shigella spp., enteropathogenic and enterohemorrhagic Escherichia coli and their murine equivalent, Citrobacter rodentium. The cellular processes or proteins targeted by the effectors can be common to multiple pathogens or pathogen-specific. The main approach to understanding T3SS-mediated pathogenesis has been to determine the contribution of one effector at a time, with the aim of piecing together individual functions and unveiling infection mechanisms. However, in contrast to this prevailing approach, simultaneous deletion of multiple effectors revealed that they function as an interconnected network in vivo, uncovering effector codependency and context-dependent effector essentiality. This paradigm shift in T3SS biology is at the heart of this opinion article.
III 型分泌系统(T3SS)效应子是许多临床重要的革兰氏阴性病原体感染策略的关键毒力因子,包括沙门氏菌、志贺氏菌属、肠致病性和肠出血性大肠杆菌及其鼠源等价物柠檬酸杆菌属。效应子靶向的细胞过程或蛋白可能对多种病原体共有,也可能具有病原体特异性。了解 T3SS 介导的发病机制的主要方法是一次确定一个效应子的贡献,目的是将各个功能整合起来,并揭示感染机制。然而,与这种流行的方法相反,同时删除多个效应子表明它们在体内作为一个相互关联的网络发挥作用,揭示了效应子的相互依存性和依赖于上下文的效应子的必要性。这种 T3SS 生物学的范式转变是本文观点的核心。