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Species-specific host factors rather than virus-intrinsic virulence determine primate lentiviral pathogenicity
ISSN
2041-1723
Date Issued
2018
Author(s)
Joas, Simone
Parrish, Erica H.
Gnanadurai, Clement W.
Lump, Edina
Stürzel, Christina M.
Parrish, Nicholas F.
Learn, Gerald H.
Sauermann, Ulrike
Neumann, Berit
Rensing, Kerstin Mätz
Fuchs, Dietmar
Billingsley, James M.
Bosinger, Steven E.
Silvestri, Guido
Apetrei, Cristian
Huot, Nicolas
Garcia-Tellez, Thalia
Müller-Trutwin, Michaela
Hotter, Dominik
Sauter, Daniel
Hahn, Beatrice H.
DOI
10.1038/s41467-018-03762-3
Abstract
HIV-1 causes chronic inflammation and AIDS in humans, whereas related simian immunodeficiency viruses (SIVs) replicate efficiently in their natural hosts without causing disease. It is currently unknown to what extent virus-specific properties are responsible for these different clinical outcomes. Here, we incorporate two putative HIV-1 virulence determinants, i.e., a Vpu protein that antagonizes tetherin and blocks NF-κB activation and a Nef protein that fails to suppress T cell activation via downmodulation of CD3, into a non-pathogenic SIVagm strain and test their impact on viral replication and pathogenicity in African green monkeys. Despite sustained high-level viremia over more than 4 years, moderately increased immune activation and transcriptional signatures of inflammation, the HIV-1-like SIVagm does not cause immunodeficiency or any other disease. These data indicate that species-specific host factors rather than intrinsic viral virulence factors determine the pathogenicity of primate lentiviruses.
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