| Literature DB >> 26996307 |
Christian Krapp1, Dominik Hotter1, Ali Gawanbacht1, Paul J McLaren2, Silvia F Kluge1, Christina M Stürzel1, Katharina Mack1, Elisabeth Reith1, Susanne Engelhart1, Angela Ciuffi3, Veit Hornung4, Daniel Sauter1, Amalio Telenti5, Frank Kirchhoff6.
Abstract
Guanylate binding proteins (GBPs) are an interferon (IFN)-inducible subfamily of guanosine triphosphatases (GTPases) with well-established activity against intracellular bacteria and parasites. Here we show that GBP5 potently restricts HIV-1 and other retroviruses. GBP5 is expressed in the primary target cells of HIV-1, where it impairs viral infectivity by interfering with the processing and virion incorporation of the viral envelope glycoprotein (Env). GBP5 levels in macrophages determine and inversely correlate with infectious HIV-1 yield over several orders of magnitude, which may explain the high donor variability in macrophage susceptibility to HIV. Antiviral activity requires Golgi localization of GBP5, but not its GTPase activity. Start codon mutations in the accessory vpu gene from macrophage-tropic HIV-1 strains conferred partial resistance to GBP5 inhibition by increasing Env expression. Our results identify GBP5 as an antiviral effector of the IFN response and may explain the increased frequency of defective vpu genes in primary HIV-1 strains.Entities:
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Year: 2016 PMID: 26996307 DOI: 10.1016/j.chom.2016.02.019
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023