Tetherin Restricts Herpes Simplex Virus 1 and Is Antagonized by Glycoprotein M

被引:55
作者
Blondeau, Caroline [1 ]
Pelchen-Matthews, Annegret [2 ]
Mlcochova, Petra [1 ,2 ]
Marsh, Mark [2 ]
Milne, Richard S. B. [1 ]
Towers, Greg J. [1 ]
机构
[1] UCL, MRC, Ctr Med Mol Virol, Div Infect & Immun, London, England
[2] UCL, MRC, Mol Cell Biol Lab, London, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
SARCOMA-ASSOCIATED HERPESVIRUS; IMMUNODEFICIENCY-VIRUS; VPU PROTEIN; HUMAN CYTOMEGALOVIRUS; HIV-1; RELEASE; TYPE-1; CELLS; DEGRADATION; INHIBITION; MECHANISM;
D O I
10.1128/JVI.02250-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tetherin is a broadly active antiviral effector that works by tethering nascent enveloped virions to a host cell membrane, thus preventing their release. In this study, we demonstrate that herpes simplex virus 1 (HSV-1) is targeted by tetherin. We identify the viral envelope glycoprotein M (gM) as having moderate anti-tetherin activity. We show that gM but not gB or gD efficiently removes tetherin from the plasma membrane and can functionally substitute for the human immunodeficiency virus type 1 (HIV-1) Vpu protein, the prototypic viral tetherin antagonist, in rescuing HIV-1 release from tetherin-expressing cells. Our data emphasize that tetherin is a broadly active antiviral effector and contribute to the emerging hypothesis that viruses must suppress or evade an array of host cell countermeasures in order to establish a productive infection.
引用
收藏
页码:13124 / 13133
页数:10
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