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

Author:

Blondeau Caroline1,Pelchen-Matthews Annegret2,Mlcochova Petra12,Marsh Mark2,Milne Richard S. B.1,Towers Greg J.1

Affiliation:

1. University College London, Medical Research Council Centre for Medical Molecular Virology, Division of Infection and Immunity, University College London, London, United Kingdom

2. MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom

Abstract

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.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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