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Tetherin Restricts Herpes Simplex Virus 1 and Is Antagonized by Glycoprotein M
Authors:Caroline Blondeau  Annegret Pelchen-Matthews  Petra Mlcochova  Mark Marsh  Richard S. B. Milne  Greg J. Towers
Affiliation:University College London, Medical Research Council Centre for Medical Molecular Virology, Division of Infection and Immunity, University College London, London, United Kingdoma;MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdomb
Abstract:
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.
Keywords:
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