Influenza A virus inhibits cytoplasmic stress granule formation

被引:116
作者
Khaperskyy, Denys A. [1 ]
Hatchette, Todd F. [1 ,2 ]
McCormick, Craig [1 ,3 ]
机构
[1] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4R2, Canada
[2] Queen Elizabeth 2 Hlth Sci Ctr, Dept Pathol & Lab Med, Halifax, NS, Canada
[3] Beatrice Hunter Canc Res Inst, Halifax, NS, Canada
基金
加拿大健康研究院;
关键词
PKR; interferon; translation; NS1; live imaging; DOUBLE-STRANDED-RNA; PROTEIN-KINASE PKR; NS1; PROTEIN; INFECTED-CELLS; MESSENGER-RNA; RIG-I; BINDING; PHOSPHORYLATION; TRANSLATION; ACTIVATION;
D O I
10.1096/fj.11-196915
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An important component of the mammalian stress response is the reprogramming of translation. A variety of stresses trigger abrupt polysome disassembly and the accumulation of stalled translation preinitiation complexes. These complexes nucleate cytoplasmic stress granules (SGs), sites of mRNA triage in which mRNAs from disassembling polysomes are sorted and the fates of individual transcripts are determined. Here, we demonstrate that influenza A virus (IAV) actively suppresses SG formation during infection, thereby allowing translation of viral mRNAs. Complete inhibition of SG formation is dependent on the function of the viral nonstructural protein 1 (NS1); at late times postinfection, cells infected with NS1-mutant viruses formed SGs in a double-stranded RNA-activated protein kinase (PKR)-dependent fashion. In these cells, SG formation correlated with inhibited viral protein synthesis. Together, these experiments demonstrate the antiviral potential of SGs and reveal a viral countermeasure that limits SG formation.-Khaperskyy, D. A., Hatchette, T. F., McCormick, C. Influenza A virus inhibits cytoplasmic stress granule formation. FASEB J. 26, 1629-1639 (2012). www.fasebj.org
引用
收藏
页码:1629 / 1639
页数:11
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