PLoS ONE (Jan 2012)

Influenza A virus does not encode a tetherin antagonist with Vpu-like activity and induces IFN-dependent tetherin expression in infected cells.

  • Michael Winkler,
  • Stephanie Bertram,
  • Kerstin Gnirß,
  • Inga Nehlmeier,
  • Ali Gawanbacht,
  • Frank Kirchhoff,
  • Christina Ehrhardt,
  • Stephan Ludwig,
  • Miriam Kiene,
  • Anna-Sophie Moldenhauer,
  • Ulrike Goedecke,
  • Christina B Karsten,
  • Annika Kühl,
  • Stefan Pöhlmann

DOI
https://doi.org/10.1371/journal.pone.0043337
Journal volume & issue
Vol. 7, no. 8
p. e43337

Abstract

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The interferon-induced host cell factor tetherin inhibits release of human immunodeficiency virus (HIV) from the plasma membrane of infected cells and is counteracted by the HIV-1 protein Vpu. Influenza A virus (FLUAV) also buds from the plasma membrane and is not inhibited by tetherin. Here, we investigated if FLUAV encodes a functional equivalent of Vpu for tetherin antagonism. We found that expression of the FLUAV protein NS1, which antagonizes the interferon (IFN) response, did not block the tetherin-mediated restriction of HIV release, which was rescued by Vpu. Similarly, tetherin-mediated inhibition of HIV release was not rescued by FLUAV infection. In contrast, FLUAV infection induced tetherin expression on target cells in an IFN-dependent manner. These results suggest that FLUAV escapes the antiviral effects of tetherin without encoding a tetherin antagonist with Vpu-like activity.