Homologous recombination is an intrinsic defense against antiviral RNA interference

被引:18
作者
Aguado, Lauren C. [1 ]
Jordan, Tristan X. [1 ]
Hsieh, Emily [1 ]
Blanco-Melo, Daniel [1 ]
Heard, John [1 ]
Panis, Maryline [1 ]
Vignuzzi, Marco [2 ]
tenOever, Benjamin R. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA
[2] Inst Pasteur, Viral Populat & Pathogenesis Unit, F-75015 Paris, France
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
RNAi; virus polarity; virus adaptation; homologous recombination; miRNA; MAMMALIAN-CELLS; READ ALIGNMENT; SUBGENOMIC RNA; VIRUS; EVOLUTION; MICRORNAS; IMMUNITY; METAGENOMICS; REPLICATION; INHIBITION;
D O I
10.1073/pnas.1810229115
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
RNA interference (RNAi) is the major antiviral defense mechanism of plants and invertebrates, rendering the capacity to evade it a defining factor in shaping the viral landscape. Here we sought to determine whether different virus replication strategies provided any inherent capacity to evade RNAi in the absence of an antagonist. Through the exploitation of host microRNAs, we recreated an RNAi-like environment in vertebrates and directly compared the capacity of positive-and negative-stranded RNA viruses to cope with this selective pressure. Applying this defense against four distinct viral families revealed that the capacity to undergo homologous recombination was the defining attribute that enabled evasion of this defense. Independent of gene expression strategy, positive-stranded RNA viruses that could undergo strand switching rapidly excised genomic material, while negative-stranded viruses were effectively targeted and cleared upon RNAi-based selection. These data suggest a dynamic relationship between host antiviral defenses and the biology of virus replication in shaping pathogen prevalence.
引用
收藏
页码:E9211 / E9219
页数:9
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