Poliovirus intrahost evolution is required to overcome tissue-specific innate immune responses

被引:54
|
作者
Xiao, Yinghong [1 ]
Dolan, Patrick Timothy [1 ,2 ]
Goldstein, Elizabeth Faul [1 ]
Li, Min [1 ]
Farkov, Mikhail [3 ,4 ]
Brodsky, Leonid [3 ,4 ]
Andino, Raul [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94158 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94158 USA
[3] Univ Haifa, Tauber Bioinformat Res Ctr, IL-31905 Haifa, Israel
[4] Univ Haifa, Dept Evolutionary & Environm Biol, IL-31905 Haifa, Israel
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
关键词
REPLICATION ELEMENT CRE; RNA VIRUSES; ALPHA/BETA-INTERFERON; MULLER RATCHET; RECOMBINATION; POPULATION; INFECTION; TROPISM; FITNESS; PATHOGENESIS;
D O I
10.1038/s41467-017-00354-5
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 viruses, such as poliovirus, have a great evolutionary capacity, allowing them to quickly adapt and overcome challenges encountered during infection. Here we show that poliovirus infection in immune-competent mice requires adaptation to tissue-specific innate immune microenvironments. The ability of the virus to establish robust infection and virulence correlates with its evolutionary capacity. We further identify a region in the multi-functional poliovirus protein 2B as a hotspot for the accumulation of minor alleles that facilitate a more effective suppression of the interferon response. We propose that population genetic dynamics enables poliovirus spread between tissues through optimization of the genetic composition of low frequency variants, which together cooperate to circumvent tissue-specific challenges. Thus, intrahost virus evolution determines pathogenesis, allowing a dynamic regulation of viral functions required to overcome barriers to infection.
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页数:12
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