Schmölders Johanna, Manske Christian, Otto Andreas, Hoffmann Christine, Steiner Bernhard, Welin Amanda, Becher Dörte, Hilbi Hubert
From the ‡Max von Pettenkofer Institute, Ludwig-Maximilians University, Munich, Germany.
§Institute for Microbiology, Ernst Moritz Arndt University, Greifswald, Germany.
Mol Cell Proteomics. 2017 Apr;16(4):622-641. doi: 10.1074/mcp.M116.063453. Epub 2017 Feb 9.
is an opportunistic bacterial pathogen that causes a severe lung infection termed "Legionnaires' disease." The pathogen replicates in environmental protozoa as well as in macrophages within a unique membrane-bound compartment, the -containing-vacuole (LCV). LCV formation requires the bacterial Icm/Dot type IV secretion system, which translocates ca. 300 "effector proteins" into host cells, where they target distinct host factors. The "pentuple" mutant (Δpentuple) lacks 5 gene clusters (31% of the effector proteins) and replicates in macrophages but not in amoeba. To elucidate the host factors defining a replication-permissive compartment, we compare here the proteomes of intact LCVs isolated from or macrophages infected with Δpentuple or the parental strain Lp02. This analysis revealed that the majority of host proteins are shared in or macrophage LCVs containing the mutant or the parental strain, respectively, whereas some proteins preferentially localize to distinct LCVs. The small GTPase Rap1 was identified on LCVs containing strain Lp02 but not the Δpentuple mutant and on macrophage LCVs containing either strain. The localization pattern of active Rap1 on or macrophage LCVs was confirmed by fluorescence microscopy and imaging flow cytometry, and the depletion of Rap1 by RNA interference significantly reduced the intracellular growth of Thus, comparative proteomics identified Rap1 as a novel LCV host component implicated in intracellular replication of .
是一种机会性细菌病原体,可引起一种称为“军团病”的严重肺部感染。该病原体在环境原生动物以及巨噬细胞内一个独特的膜结合区室——含军团菌液泡(LCV)中进行复制。LCV的形成需要细菌的Icm/Dot IV型分泌系统,该系统将约300种“效应蛋白”转运到宿主细胞中,在那里它们靶向不同的宿主因子。“五重”突变体(Δ五重)缺乏5个基因簇(占效应蛋白的31%),可在巨噬细胞中复制,但不能在变形虫中复制。为了阐明定义允许复制区室的宿主因子,我们在此比较了从感染Δ五重或亲本菌株Lp02的阿米巴或巨噬细胞中分离出的完整LCV的蛋白质组。该分析表明,大多数宿主蛋白分别在含有突变体或亲本菌株的阿米巴或巨噬细胞LCV中共享,而一些蛋白优先定位于不同的LCV。小GTP酶Rap1在含有菌株Lp02的阿米巴LCV上被鉴定出来,但在Δ五重突变体上未被鉴定出来,并且在含有任一菌株的巨噬细胞LCV上也被鉴定出来。通过荧光显微镜和成像流式细胞术证实了活性Rap1在阿米巴或巨噬细胞LCV上的定位模式,并且通过RNA干扰耗尽Rap1显著降低了嗜肺军团菌的细胞内生长。因此,比较蛋白质组学确定Rap1是一种与嗜肺军团菌细胞内复制有关的新型LCV宿主成分。