Drexel Institute for Biotechnology and Virology Research, Department of Microbiology and Immunology, Drexel University College of Medicine, 3805 Old Easton Road, Doylestown, PA 18902, USA.
J Virol. 2010 Dec;84(24):12646-57. doi: 10.1128/JVI.01328-10. Epub 2010 Oct 13.
Tetherin and IFITM3 are recently identified interferon-induced cellular proteins that restrict infections by retroviruses and filoviruses and of influenza virus and flaviviruses, respectively. In our efforts to further explore their antiviral activities against other viruses and determine their antiviral mechanisms, we found that the two antiviral proteins potently inhibit the infection of vesicular stomatitis virus (VSV), a prototype member of the Rhabdoviridae family. Taking advantage of this well-studied virus infection system, we show that although both tetherin and IFITM3 are plasma membrane proteins, tetherin inhibits virion particle release from infected cells, while IFITM3 disrupts an early event after endocytosis of virion particles but before primary transcription of incoming viral genomes. Furthermore, we demonstrate that both the N-terminal 21 amino acid residues and C-terminal transmembrane region of IFITM3 are required for its antiviral activity. Collectively, our work sheds light on the mechanisms by which tetherin and IFITM3 restrict infection with rhabdoviruses and possibly other pathogenic viruses.
tetherin 和 IFITM3 是最近发现的干扰素诱导的细胞蛋白,分别能限制逆转录病毒和丝状病毒、流感病毒和黄病毒的感染。在进一步探索它们对其他病毒的抗病毒活性和确定其抗病毒机制的过程中,我们发现这两种抗病毒蛋白能有效抑制水疱性口炎病毒(VSV)的感染,VSV 是 Rhabdoviridae 科的一个原型成员。利用这个研究充分的病毒感染系统,我们表明,尽管 tetherin 和 IFITM3 都是质膜蛋白,但 tetherin 抑制感染细胞中病毒粒子的释放,而 IFITM3 则破坏病毒粒子内化后的早期事件,但在进入的病毒基因组的初级转录之前。此外,我们证明 IFITM3 的 N 端 21 个氨基酸残基和 C 端跨膜区都是其抗病毒活性所必需的。总之,我们的工作阐明了 tetherin 和 IFITM3 限制 Rhabdoviridae 病毒和可能其他致病病毒感染的机制。