The Nef Protein of the Macrophage Tropic HIV-1 Strain AD8 Counteracts Human BST-2/Tetherin

• Published in: Viruses 2020-04, Vol.12 (4), p.459
• Main Authors: Giese, Sebastian, Lawrence, Scott P, Mazzon, Michela, Nijmeijer, Bernadien M, Marsh, Mark
• Format: Article
• Language: English
• Subjects: Antigens, CD - genetics; Antigens, CD - metabolism; BST-2; Cell Line; Chemical properties; Fluorescent Antibody Technique; Gene Expression; Glycoproteins; GPI-Linked Proteins - genetics; GPI-Linked Proteins - metabolism; Health aspects; HIV; HIV Infections - immunology; HIV Infections - metabolism; HIV Infections - virology; HIV-1; HIV-1 - physiology; Host-Pathogen Interactions; Humans; Macrophages; Macrophages - immunology; Macrophages - metabolism; Macrophages - virology; Nef; nef Gene Products, Human Immunodeficiency Virus - chemistry; nef Gene Products, Human Immunodeficiency Virus - metabolism; PBMC; Physiological aspects; Protein Binding; Protein Interaction Domains and Motifs; tetherin; Viral proteins
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v12040459

Bone Marrow Stromal Cell Antigen 2 (BST-2)/tetherin inhibits the release of numerous enveloped viruses by physically tethering nascent particles to infected cells during the process of viral budding from the cell surface. Tetherin also restricts human immunodeficiency virus (HIV), and pandemic main (M) group HIV type 1s (HIV-1s) are thought to rely exclusively on their Vpu proteins to overcome tetherin-mediated restriction of virus release. However, at least one M group HIV-1 strain, the macrophage-tropic primary AD8 isolate, is unable to express Vpu due to a mutation in its translation initiation codon. Here, using primary monocyte-derived macrophages (MDMs), we show that AD8 Nef protein can compensate for the absence of Vpu and restore virus release to wild type levels. We demonstrate that HIV-1 AD8 Nef reduces endogenous cell surface tetherin levels, physically separating it from the site of viral budding, thus preventing HIV retention. Mechanistically, AD8 Nef enhances internalisation of the long isoform of human tetherin, leading to perinuclear accumulation of the restriction factor. Finally, we show that Nef proteins from other HIV strains also display varying degrees of tetherin antagonism. Overall, we show that M group HIV-1s can use an accessory protein other than Vpu to antagonise human tetherin.