Liss Viktoria, Hensel Michael
Abteilung Mikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Barbarastr. 11, Osnabrück, 49076, Germany.
Cell Microbiol. 2015 May;17(5):639-47. doi: 10.1111/cmi.12441. Epub 2015 Apr 10.
Salmonella enterica is a facultative intracellular pathogen residing in a unique host cell-derived membrane compartment, termed Salmonella-containing vacuole or SCV. By the activity of effector proteins translocated by the SPI2-endoced type III secretion system (T3SS), the biogenesis of the SCV is manipulated to generate a habitat permissive for intracellular proliferation. By taking control of the host cell vesicle fusion machinery, intracellular Salmonella creates an extensive interconnected system of tubular membranes arising from vesicles of various origins, collectively termed Salmonella-induced tubules (SIT). Recent work investigated the dynamic properties of these manipulations. New host cell targets of SPI2-T3SS effector proteins were identified. By applying combinations of live cell imaging and ultrastructural analyses, the detailed organization of membrane compartments inhabited and modified by intracellular Salmonella is now available. These studies provided unexpected new details on the intracellular environments of Salmonella. For example, one kind of SIT, the LAMP1-positive Salmonella-induced filaments (SIF), are composed of double-membrane tubules, with an inner lumen containing host cell cytosol and cytoskeletal filaments, and an outer lumen containing endocytosed cargo. The novel findings call for new models for the biogenesis of SCV and SIT and give raise to many open questions we discuss in this review.
肠炎沙门氏菌是一种兼性细胞内病原体,存在于一种独特的宿主细胞衍生的膜区室中,称为含沙门氏菌液泡或SCV。通过SPI2编码的III型分泌系统(T3SS)转运的效应蛋白的活性,SCV的生物发生被操纵以产生一个允许细胞内增殖的栖息地。通过控制宿主细胞囊泡融合机制,细胞内沙门氏菌产生了一个由各种来源的囊泡产生的广泛相互连接的管状膜系统,统称为沙门氏菌诱导小管(SIT)。最近的研究调查了这些操纵的动态特性。确定了SPI2-T3SS效应蛋白的新宿主细胞靶点。通过应用活细胞成像和超微结构分析的组合,现在可以了解细胞内沙门氏菌占据和修饰的膜区室的详细组织。这些研究提供了关于沙门氏菌细胞内环境的意外新细节。例如,一种SIT,即LAMP1阳性沙门氏菌诱导丝(SIF),由双膜小管组成,其内腔含有宿主细胞胞质溶胶和细胞骨架丝,外腔含有内吞货物。这些新发现需要新的SCV和SIT生物发生模型,并引发了我们在本综述中讨论的许多未解决的问题。