Antagonism of CD317 restriction of human immunodeficiency virus type 1 (HIV-1) particle release and depletion of CD317 are separable activities of HIV-1 Vpu

  • Christine Goffinet
  • , Stefanie Homann
  • , Ina Ambiel
  • , Nadine Tibroni
  • , Daniel Rupp
  • , Oliver T. Keppler
  • , Oliver T. Fackler

Research output: Contribution to journalArticlepeer-review

70 Citations (Scopus)

Abstract

Vpu antagonizes human immunodeficiency virus type 1 (HIV-1) particle release inhibition by CD317/BST- 2/Tetherin. Whether this Vpu activity strictly requires cellular depletion of the restriction factor is unclear. Here, we characterized CD317 variants with mutations in putative sorting or ubiquitination motifs. All mutants still potently impaired release of Vpu-defective HIV-1 and remained sensitive to Vpu-mediated release enhancement. Importantly, this virological antagonism correlated with surface downregulation of CD317 mutants by Vpu, while intracellular pools of these mutants, which were consistently depleted of the wild-type protein, were highly variable or even enhanced. Thus, Vpu can efficiently antagonize virion tethering in the absence of CD317 degradation.
Original languageEnglish
Pages (from-to)4089-4094
Number of pages6
JournalJournal of Virology
Volume84
Issue number8
DOIs
Publication statusPublished - 1 Apr 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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