z-logo
open-access-imgOpen Access
Tetherin Restricts Herpes Simplex Virus 1 and Is Antagonized by Glycoprotein M
Author(s) -
Caroline Blondeau,
Annegret Pelchen–Matthews,
Petra Mlčochová,
Mark Marsh,
R Milne,
Greg J. Towers
Publication year - 2013
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.02250-13
Subject(s) - tetherin , biology , effector , virology , viral envelope , herpes simplex virus , glycoprotein , herpesvirus glycoprotein b , virus , viral entry , microbiology and biotechnology , membrane glycoproteins , antiviral protein , viral replication , genetics , gene , rna
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom