Chen Lin, Wang Chengmin, Luo Jing, Li Meng, Liu Huimin, Zhao Na, Huang Jingjing, Zhu Xili, Ma Guoyao, Yuan Guohui, He Hongxuan
National Research Center for Wildlife-Borne Diseases, Institute of Zoology, Chinese Academy of SciencesBeijing, China.
University of the Chinese Academy of SciencesBeijing, China.
Front Microbiol. 2017 Jul 11;8:1308. doi: 10.3389/fmicb.2017.01308. eCollection 2017.
H5N1 is a highly pathogenic influenza A virus (IAV) and poses a major threat to the public health. The nucleoprotein (NP) has a multiple functions during the viral life cycle, however, the precise role of NP mutants in viral replication and pathogenicity is not completely understood. Here, we attempted to identify five residues in NP that may contribute to viral replication or pathogenicity. Of these, K227R, K229R, and K470R viruses were successfully rescued by reverse genetic, but the K91R and K198R viruses were not viable. A mini-genome assay demonstrated that the NP mutations K91R and K198R significantly decreased the polymerase activity. Moreover, these two mutations resulted in disrupted cellular localization in mammalian cells. Importantly, mutation at position 470 of NP significantly increased its virulence and . These findings demonstrated that the NP protein plays a major role in influenza virulence and pathogenicity, which adds to the knowledge of IAV virulence determinants and may benefit IAV surveillance.
H5N1是一种高致病性甲型流感病毒(IAV),对公众健康构成重大威胁。核蛋白(NP)在病毒生命周期中具有多种功能,然而,NP突变体在病毒复制和致病性方面的确切作用尚未完全明确。在此,我们试图确定NP中可能有助于病毒复制或致病性的五个残基。其中,K227R、K229R和K470R病毒通过反向遗传学成功拯救,但K91R和K198R病毒无法存活。一个微型基因组试验表明,NP突变K91R和K198R显著降低了聚合酶活性。此外,这两个突变导致哺乳动物细胞中的细胞定位紊乱。重要的是,NP第470位的突变显著增加了其毒力。这些发现表明,NP蛋白在流感病毒的毒力和致病性中起主要作用,这增加了对IAV毒力决定因素的认识,并可能有益于IAV监测。