| Literature DB >> 29677653 |
Jing Li1, Kun Zhang2, Quanjiao Chen3, Xiaoshuang Zhang3, Yeping Sun4, Yuhai Bi4, Shuang Zhang4, Jinyan Gu5, Jiarong Li5, Di Liu6, Wenjun Liu7, Jiyong Zhou8.
Abstract
Influenza A viruses have sophisticated strategies to promote their own replication. Here, we found that three H5N1 influenza viruses display different replication patterns in human A549 and macrophage cells. The HN01 virus displayed poor replication compared to HN021 and JS01. In addition, the HN01 virus was unable to counteract the interferon response and block general gene expression. This capability was restored by three amino acid substitutions on the NS1 protein: K55E, K66E, and C133F, resulting in recovered binding to CPSF30 and decreased interferon response activity. Furthermore, a recombinant HN01 virus expressing either NS1-C133F or the triple mutation replicate with higher titers in human A549 cells and macrophages compared to the parent virus. These three amino acid mutations reveal a new pathway to alter H5N1 virus replication.Entities:
Keywords: H5N1 influenza virus; IFN response; NS1 protein; Virus replication
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Year: 2018 PMID: 29677653 DOI: 10.1016/j.virol.2018.04.004
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616