Comparative RNAi Screening Reveals Host Factors Involved in Enterovirus Infection of Polarized Endothelial Monolayers

被引:61
作者
Coyne, Carolyn B. [1 ]
Bozym, Rebecca [1 ]
Morosky, Stefanie A. [1 ]
Hanna, Sheri L. [3 ]
Mukherjee, Amitava [1 ]
Tudor, Matthew
Kim, Kwang Sik [2 ]
Cherry, Sara [3 ]
机构
[1] Univ Pittsburgh, Dept Microbiol & Mol Genet, Pittsburgh, PA 15219 USA
[2] Johns Hopkins Univ, Sch Med, Div Pediat Infect Dis, Baltimore, MD 21287 USA
[3] Univ Penn, Penn Genome Frontiers Inst, Dept Microbiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
COXSACKIEVIRUS ENTRY; SMALL GTPASE; MYOSIN-VI; GENES; CELLS; IDENTIFICATION; TRANSCRIPTION; TRANSCYTOSIS; ACTIVATION; PROTEINS;
D O I
10.1016/j.chom.2011.01.001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Enteroviruses, including coxsackievirus B (CVB) and poliovirus (PV), can access the CNS through the blood brain barrier (BBB) endothelium to cause aseptic meningitis. To identify cellular components required for CVB and PV infection of human brain microvascular endothelial cells, an in vitro BBB model, we performed comparative RNAi screens and identified 117 genes that influenced infection. Whereas a large proportion of genes whose depletion enhanced infection (17 of 22) were broadly anti-enteroviral, only 46 of the 95 genes whose depletion inhibited infection were required by both CVB and PV and included components of cell signaling pathways such as adenylate cyclases. Downregulation of genes including Rab GTPases, Src tyrosine kinases, and tyrosine phosphatases displayed specificity in their requirement for either CVB or PV infection. These findings highlight the pathways hijacked by enteroviruses for entry and replication in the BBB endothelium, a specialized and clinically relevant cell type for these viruses.
引用
收藏
页码:70 / 82
页数:13
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