Innate immune evasion strategies of DNA and RNA viruses

被引:163
|
作者
Beachboard, Dia C. [1 ]
Horner, Stacy M. [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
HEPATITIS-C-VIRUS; INFLUENZA-A VIRUS; RIG-I; DENDRITIC CELLS; REPLICATION COMPLEX; RECEPTOR ACTIVATION; ANTIVIRAL PATHWAY; SENSING PATHWAY; ADAPTER PROTEIN; PHOSPHATASE PP1;
D O I
10.1016/j.mib.2016.05.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Upon infection, both DNA and RNA viruses can be sensed by pattern recognition receptors (PRRs) in the cytoplasm or the nucleus to activate antiviral innate immunity. Sensing of viral products leads to the activation of a signaling cascade that ultimately results in transcriptional activation of type I and Ill interferons, as well as other antiviral genes that together mediate viral clearance and inhibit viral spread. Therefore, in order for viruses to replicate and spread efficiently, they must inhibit the host signaling pathways that induce the innate antiviral immune response. In this review, we will highlight recent advances in the understanding of the mechanisms by which viruses evade PRR detection, intermediate signaling molecule activation, transcription factor activation, and the actions of antiviral proteins.
引用
收藏
页码:113 / 119
页数:7
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