Sakuma Toshie, Noda Takeshi, Urata Shuzo, Kawaoka Yoshihiro, Yasuda Jiro
First Department of Forensic Science, National Research Institute of Police Science, Kashiwa 277-0882, Japan.
J Virol. 2009 Mar;83(5):2382-5. doi: 10.1128/JVI.01607-08. Epub 2008 Dec 17.
Recently, tetherin has been identified as an effective cellular factor that prevents the release of human immunodeficiency virus type 1. Here, we show that the production of virus-like particles induced by viral matrix proteins of Lassa virus or Marburg virus was markedly inhibited by tetherin and that N-linked glycosylation of tetherin was dispensable for this antiviral activity. Our data also suggest that viral matrix proteins or one or more components that originate from host cells are targets of tetherin but that viral surface glycoproteins are not. These results suggest that tetherin inhibits the release of a wide variety of enveloped viruses from host cells by a common mechanism.
最近,束缚素已被确定为一种有效的细胞因子,可阻止1型人类免疫缺陷病毒的释放。在此,我们表明,拉沙病毒或马尔堡病毒的病毒基质蛋白诱导产生的病毒样颗粒被束缚素显著抑制,并且束缚素的N-连接糖基化对于这种抗病毒活性是可有可无的。我们的数据还表明,病毒基质蛋白或源自宿主细胞的一种或多种成分是束缚素的靶标,但病毒表面糖蛋白不是。这些结果表明,束缚素通过一种共同机制抑制多种包膜病毒从宿主细胞中释放。