Activation of the Antiviral Kinase PKR and Viral Countermeasures

被引:106
作者
Dauber, Bianca [1 ]
Wolff, Thorsten [2 ]
机构
[1] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB T6G 2S2, Canada
[2] Robert Koch Inst, D-13353 Berlin, Germany
来源
VIRUSES-BASEL | 2009年 / 1卷 / 03期
关键词
PKR; virus; dsRNA; innate immunity; immune evasion; DOUBLE-STRANDED-RNA; VIRUS NS1 PROTEIN; INFLUENZA-A VIRUS; MURINE CYTOMEGALOVIRUS M142; HERPES-SIMPLEX-VIRUS; EBOLA-VIRUS; RIG-I; MESSENGER-RNA; VP35; PROTEIN; B VIRUS;
D O I
10.3390/v1030523
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
The interferon-induced double-stranded (ds) RNA-dependent protein kinase (PKR) limits viral replication by an eIF2 alpha-mediated block of translation. Although many negative-strand RNA viruses activate PKR, the responsible RNAs have long remained elusive, as dsRNA, the canonical activator of PKR, has not been detected in cells infected with such viruses. In this review we focus on the activating RNA molecules of different virus families, in particular the negative-strand RNA viruses. We discuss the recently identified non-canonical activators 5'-triphosphate RNA and the vRNP of influenza virus and give an update on strategies of selected RNA and DNA viruses to prevent activation of PKR.
引用
收藏
页码:523 / 544
页数:22
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