Host-Pathogen Interactions and Immunity to Infection, Institute for Advanced Biosciences (IAB), INSERM U1209, CNRS UMR 5309, Grenoble Alpes University, Grenoble, France; email:
Annu Rev Microbiol. 2022 Sep 8;76:135-155. doi: 10.1146/annurev-micro-041320-011520. Epub 2022 May 19.
Like many intracellular pathogens, the protozoan parasite has evolved sophisticated mechanisms to promote its transmission and persistence in a variety of hosts by injecting effector proteins that manipulate many processes in the cells it invades. Specifically, the parasite diverts host epigenetic modulators and modifiers from their native functions to rewire host gene expression to counteract the innate immune response and to limit its strength. The arms race between the parasite and its hosts has led to accelerated adaptive evolution of effector proteins and the unconventional secretion routes they use. This review provides an up-to-date overview of how effectors, through the evolution of intrinsically disordered domains, the formation of supramolecular complexes, and the use of molecular mimicry, target host transcription factors that act as coordinating nodes, as well as chromatin-modifying enzymes, to control the fate of infected cells and ultimately the outcome of infection.
像许多细胞内病原体一样,原生动物寄生虫已经进化出复杂的机制,通过注射效应蛋白来促进其在各种宿主中的传播和持续存在,这些效应蛋白可以操纵其入侵的细胞中的许多过程。具体来说,寄生虫会将宿主的表观遗传调节剂和修饰剂从其固有功能中转移出来,重新连接宿主基因表达,以对抗先天免疫反应并限制其强度。寄生虫与其宿主之间的军备竞赛导致了效应蛋白及其使用的非常规分泌途径的加速适应性进化。这篇综述提供了最新的概述,说明效应蛋白如何通过内在无序结构域的进化、超分子复合物的形成以及分子模拟的使用,靶向作为协调节点的宿主转录因子以及染色质修饰酶,来控制感染细胞的命运,并最终控制感染的结果。