Katsura Hiroaki, Fukuyama Satoshi, Watanabe Shinji, Ozawa Makoto, Neumann Gabriele, Kawaoka Yoshihiro
Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Exploratory Research for Advanced Technology, Infection-Induced Host Responses Project, Japan Science and Technology Agency, Saitama, Japan.
Sci Rep. 2016 Feb 5;6:19933. doi: 10.1038/srep19933.
Influenza viruses that express reporter proteins are useful tools, but are often attenuated. Recently, we found that an influenza virus encoding the Venus fluorescent protein acquired two mutations in its PB2 and HA proteins upon mouse adaptation. Here, we demonstrate that the enhanced viral replication and virulence in mice of this Venus-expressing influenza virus are primarily conferred by the PB2-E712D mutation, with only a minor contribution by the HA-T380A mutation.
表达报告蛋白的流感病毒是有用的工具,但往往减毒。最近,我们发现一种编码维纳斯荧光蛋白的流感病毒在适应小鼠后其PB2和HA蛋白发生了两个突变。在这里,我们证明这种表达维纳斯的流感病毒在小鼠体内增强的病毒复制和毒力主要由PB2-E712D突变赋予,而HA-T380A突变的贡献较小。