Systematic Identification of Host Cell Regulators of Legionella pneumophila Pathogenesis Using a Genome-wide CRISPR Screen

被引:68
作者
Jeng, Edwin E. [1 ,2 ]
Bhadkamkar, Varun [3 ]
Lbe, Nnejiuwa U. [3 ]
Gause, Haley [3 ]
Jiang, Lihua [1 ]
Chan, Joanne [1 ]
Jian, Ruiqi [1 ]
Jimenez-Morales, David [4 ,5 ,6 ,7 ]
Stevenson, Erica [4 ,5 ,6 ]
Krogan, Nevan J. [4 ,5 ,6 ]
Swaney, Danielle L. [4 ,5 ,6 ]
Snyder, Michael P. [1 ]
Mukherjee, Shaeri [3 ]
Bassik, Michael C. [1 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Program Canc Biol, Stanford, CA 94305 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, QBI, San Francisco, CA 94143 USA
[6] J David Gladstone Inst, San Francisco, CA USA
[7] Stanford Univ, Div Cardiovasc Med, Dept Med, Stanford, CA 94305 USA
关键词
EFFECTOR PROTEINS; RAB GTPASES; PHAGOCYTOSIS; PHAGOSOME; TRANSPORT; PHOSPHATIDYLINOSITOL-4,5-BISPHOSPHATE; UBIQUITINATION; MACROPHAGES; TRAFFICKING; MODULATION;
D O I
10.1016/j.chom.2019.08.017
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During infection, Legionella pneumophila translocates over 300 effector proteins into the host cytosol, allowing the pathogen to establish an endoplasmic reticulum (ER)-like Legionella-containing vacuole (LCV) that supports bacterial replication. Here, we perform a genome-wide CRISPR-Cas9 screen and secondary targeted screens in U937 human monocyte/macrophage-like cells to systematically identify host factors that regulate killing by L. pneumophila. The screens reveal known host factors hijacked by L. pneumophila, as well as genes spanning diverse trafficking and signaling pathways previously not linked to L. pneumophila pathogenesis. We further characterize C1orf43 and KIAA1109 as regulators of phagocytosis and show that RAB10 and its chaperone RABIF are required for optimal L. pneumophila replication and ER recruitment to the LCV. Finally, we show that Rab10 protein is recruited to the LCV and ubiquitinated by the effectors SidC/SdcA. Collectively, our results provide a wealth of previously undescribed insights into L. pneumophila pathogenesis and mammalian cell function.
引用
收藏
页码:551 / +
页数:19
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