Human genome-wide RNAi screen reveals host factors required for enterovirus 71 replication

被引:50
|
作者
Wu, Kan Xing [1 ]
Phuektes, Patchara [1 ]
Kumar, Pankaj [2 ]
Goh, Germaine Yen Lin [2 ]
Moreau, Dimitri [2 ]
Chow, Vincent Tak Kwong [1 ]
Bard, Frederic [2 ]
Chu, Justin Jang Hann [1 ,2 ]
机构
[1] Natl Univ Singapore, Dept Microbiol & Immunol, Singapore 117597, Singapore
[2] Agcy Sci Technol & Res, Inst Mol & Cell Biol, Singapore 138673, Singapore
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
英国医学研究理事会;
关键词
RIBOSOMAL ENTRY SITE; PEPTIDE-N-GLYCANASE; ERM PROTEINS; AURORA-B; INFECTION; BINDS; INHIBITOR; AUTOPHAGY; RECEPTOR; RADIXIN;
D O I
10.1038/ncomms13150
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enterovirus 71 (EV71) is a neurotropic enterovirus without antivirals or vaccine, and its host-pathogen interactions remain poorly understood. Here we use a human genome-wide RNAi screen to identify 256 host factors involved in EV71 replication in human rhabdomyosarcoma cells. Enrichment analyses reveal overrepresentation in processes like mitotic cell cycle and transcriptional regulation. We have carried out orthogonal experiments to characterize the roles of selected factors involved in cell cycle regulation and endoplasmatic reticulum-associated degradation. We demonstrate nuclear egress of CDK6 in EV71 infected cells, and identify CDK6 and AURKB as resistance factors. NGLY1, which co-localizes with EV71 replication complexes at the endoplasmatic reticulum, supports EV71 replication. We confirm importance of these factors for EV71 replication in a human neuronal cell line and for coxsackievirus A16 infection. A small molecule inhibitor of NGLY1 reduces EV71 replication. This study provides a comprehensive map of EV71 host factors and reveals potential antiviral targets.
引用
收藏
页数:13
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