Mao Dexin, Yan Feixiang, Zhang Xiaolin, Gao Guangxia
CAS Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Chaoyang District, Beijing 100101, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
iScience. 2022 Feb 1;25(2):103843. doi: 10.1016/j.isci.2022.103843. eCollection 2022 Feb 18.
Enveloped viruses pose constant threat to hosts from ocean to land. Virion particle release from cell surface is a critical step in the viral life cycle for most enveloped viruses, making it a common antiviral target for the host defense system. Here we report that host factor TMEM106A inhibits the release of enveloped viruses from the cell surface. TMEM106A is a type II transmembrane protein localized on the plasma membrane and can be incorporated into HIV-1 virion particles. Through intermolecular interactions of its C-terminal domains on virion particle and plasma membrane, TMEM106A traps virion particles to the cell surface. HIV-1 Env interacts with TMEM106A to interfere with the intermolecular interactions and partially suppresses its antiviral activity. TMEM106A orthologs from various species displayed potent antiviral activity against multiple enveloped viruses. These results suggest that TMEM106A is an evolutionarily conserved antiviral factor that inhibits the release of enveloped viruses from the cell surface.
包膜病毒对从海洋到陆地的宿主构成持续威胁。对于大多数包膜病毒而言,病毒粒子从细胞表面释放是病毒生命周期中的关键步骤,这使其成为宿主防御系统常见的抗病毒靶点。在此我们报告,宿主因子TMEM106A可抑制包膜病毒从细胞表面释放。TMEM106A是一种定位在质膜上的II型跨膜蛋白,可被整合到HIV-1病毒粒子中。通过其在病毒粒子和质膜上的C端结构域的分子间相互作用,TMEM106A将病毒粒子捕获在细胞表面。HIV-1包膜蛋白(Env)与TMEM106A相互作用以干扰分子间相互作用,并部分抑制其抗病毒活性。来自不同物种的TMEM106A直系同源物对多种包膜病毒显示出强大的抗病毒活性。这些结果表明,TMEM106A是一种进化上保守的抗病毒因子,可抑制包膜病毒从细胞表面释放。