HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation
Program in Molecular Medicine
Animals; Cell Line; Cell Membrane; Endosomes; Evolution, Molecular; Gene Products, gag; Gene Products, nef; HIV-1; Host Specificity; *Host-Pathogen Interactions; Humans; Leukemia Virus, Murine; Membrane Proteins; Neoplasm Proteins; Primates; Receptors, Cell Surface; Virion; nef Gene Products, Human Immunodeficiency Virus; rab GTP-Binding Proteins
Biochemistry | Molecular Biology
HIV-1 Nef, a protein important for the development of AIDS, has well-characterized effects on host membrane trafficking and receptor downregulation. By an unidentified mechanism, Nef increases the intrinsic infectivity of HIV-1 virions in a host-cell-dependent manner. Here we identify the host transmembrane protein SERINC5, and to a lesser extent SERINC3, as a potent inhibitor of HIV-1 particle infectivity that is counteracted by Nef. SERINC5 localizes to the plasma membrane, where it is efficiently incorporated into budding HIV-1 virions and impairs subsequent virion penetration of susceptible target cells. Nef redirects SERINC5 to a Rab7-positive endosomal compartment and thereby excludes it from HIV-1 particles. The ability to counteract SERINC5 was conserved in Nef encoded by diverse primate immunodeficiency viruses, as well as in the structurally unrelated glycosylated Gag from murine leukaemia virus. These examples of functional conservation and convergent evolution emphasize the fundamental importance of SERINC5 as a potent anti-retroviral factor.
DOI of Published Version
Nature. 2015 Oct 8;526(7572):212-7. doi: 10.1038/nature15399. Epub 2015 Sep 30. Link to article on publisher's site
Rosa, Annachiara; Chande, Ajit; Ziglio, Serena; De Sanctis, Veronica; Bertorelli, Roberto; Goh, Shih Lin; McCauley, Sean M.; Nowosielska, Anetta; Antonarakis, Stylianos E.; Luban, Jeremy; Santoni, Federico Andrea; and Pizzato, Massimo, "HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation" (2015). Program in Molecular Medicine Publications and Presentations. 56.