| Literature DB >> 32763144 |
Jianxiong Zeng1, Shupeng Dong2, Zhifei Luo1, Xiaochun Xie1, Bishi Fu3, Ping Li4, Chengrong Liu5, Xing Yang5, Yujie Chen6, Xin Wang5, Zhenshan Liu5, Jing Wu7, Youzhen Yan1, Feng Wang2, Jian-Fu Chen8, Jian Zhang7, Gang Long6, Steven A Goldman9, Shitao Li10, Zhen Zhao11, Qiming Liang12.
Abstract
Zika virus (ZIKV) causes microcephaly and disrupts neurogenesis. Dicer-mediated miRNA biogenesis is required for embryonic brain development and has been suggested to be disrupted upon ZIKV infection. Here we mapped the ZIKV-host interactome in neural stem cells (NSCs) and found that Dicer is specifically targeted by the capsid from ZIKV, but not other flaviviruses, to facilitate ZIKV infection. We identified a capsid mutant (H41R) that loses this interaction and does not suppress Dicer activity. Consistently, ZIKV-H41R is less virulent and does not inhibit neurogenesis in vitro or corticogenesis in utero. Epidemic ZIKV strains contain capsid mutations that increase Dicer binding affinity and enhance pathogenicity. ZIKV-infected NSCs show global dampening of miRNA production, including key miRNAs linked to neurogenesis, which is not observed after ZIKV-H41R infection. Together these findings show that capsid-dependent suppression of Dicer is a major determinant of ZIKV immune evasion and pathogenesis and may underlie ZIKV-related microcephaly.Entities:
Keywords: Dicer; Zika virus; capsid; miRNA; microcephaly
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Year: 2020 PMID: 32763144 PMCID: PMC7541724 DOI: 10.1016/j.stem.2020.07.012
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633