Steiner Bernhard, Swart A Leoni, Hilbi Hubert
Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland.
Methods Mol Biol. 2019;1921:221-238. doi: 10.1007/978-1-4939-9048-1_14.
Legionella pneumophila is a facultative intracellular bacterium, which grows in amoebae as well as in macrophages and epithelial cells. Depletion of genes of interest by RNA interference (RNAi) has proven to be a robust and economic technique to study L. pneumophila-host cell interactions. Predesigned and often validated double-stranded (ds) RNA oligonucleotides that silence specific genes are commercially available. RNAi results in a reduced level of distinct proteins, which allows studying the specific role of host cell components involved in L. pneumophila infection. Here, we describe how to assess RNAi-mediated protein depletion efficiency and cytotoxic effects in human A549 lung epithelial cells and murine RAW 264.7 macrophages. Moreover, we demonstrate how RNAi can be used to screen for novel host cell proteins involved in the formation of the Legionella-containing vacuole and intracellular replication of the pathogen.
嗜肺军团菌是一种兼性细胞内细菌,它可在变形虫以及巨噬细胞和上皮细胞中生长。通过RNA干扰(RNAi)耗尽感兴趣的基因已被证明是研究嗜肺军团菌与宿主细胞相互作用的一种强大且经济的技术。可商购到预先设计且通常经过验证的双链(ds)RNA寡核苷酸,它们可使特定基因沉默。RNAi导致特定蛋白质水平降低,这有助于研究参与嗜肺军团菌感染的宿主细胞成分的特定作用。在此,我们描述了如何评估RNAi介导的蛋白质消耗效率以及对人A549肺上皮细胞和小鼠RAW 264.7巨噬细胞的细胞毒性作用。此外,我们展示了如何使用RNAi筛选参与含军团菌液泡形成和病原体细胞内复制的新型宿主细胞蛋白。