BST-2 restricts IAV release and is countered by the viral M2 protein

Biochem J. 2017 Feb 20;474(5):715-730. doi: 10.1042/BCJ20160861.

Abstract

BST-2 (tetherin, CD317, and HM1.24) is induced by interferon and restricts virus release by tethering the enveloped viruses to the cell surface. The effect of BST-2 on influenza A virus (IAV) infection has been inconclusive. In the present study, we report that BST-2 diminishes the production of IAV virus-like particles (VLPs) that are generated by viral neuraminidase and hemagglutinin proteins to a much greater degree than it inhibits the production of wild-type IAV particles. This relatively weaker inhibition of IAV is associated with reduction in BST-2 levels, which is caused by the M2 protein that interacts with BST-2 and leads to down-regulation of cell surface BST-2 via the proteasomal pathway. Similarly to the viral antagonist Vpu, M2 also rescues the production of human immunodeficiency virus-1 VLPs and IAV VLPs in the presence of BST-2. Replication of wild-type and the M2-deleted viruses were both inhibited by BST-2, with the M2-deleted IAV being more restricted. These data reveal one mechanism that IAV employs to counter restriction by BST-2.

Keywords: BST-2; M2; host restriction factors; influenza virus; innate immunity.

MeSH terms

  • Animals
  • Antigens, CD / genetics*
  • Antigens, CD / metabolism
  • Chlorocebus aethiops
  • Dogs
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / metabolism
  • Gene Expression Regulation
  • HEK293 Cells
  • HIV-1 / genetics*
  • HIV-1 / metabolism
  • HeLa Cells
  • Hemagglutinin Glycoproteins, Influenza Virus / genetics
  • Hemagglutinin Glycoproteins, Influenza Virus / metabolism
  • Host-Pathogen Interactions*
  • Humans
  • Influenza A Virus, H1N1 Subtype / genetics*
  • Influenza A Virus, H1N1 Subtype / metabolism
  • Madin Darby Canine Kidney Cells
  • Neuraminidase / genetics
  • Neuraminidase / metabolism
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Proteasome Endopeptidase Complex / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Signal Transduction
  • Transfection
  • Vero Cells
  • Viral Matrix Proteins / genetics*
  • Viral Matrix Proteins / metabolism
  • Virion / genetics
  • Virion / metabolism
  • Virus Release / genetics

Substances

  • Antigens, CD
  • BST2 protein, human
  • GPI-Linked Proteins
  • Hemagglutinin Glycoproteins, Influenza Virus
  • M2 protein, Influenza A virus
  • Recombinant Proteins
  • Viral Matrix Proteins
  • hemagglutinin, human influenza A virus
  • Neuraminidase
  • Proteasome Endopeptidase Complex

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