| Literature DB >> 32849468 |
Kimberly Schmitt1, James Curlin1, Leila Remling-Mulder1, Ryan Moriarty2, Kelly Goff3, Shelby O'Connor2, Mark Stenglein1, Preston Marx3,4, Ramesh Akkina1.
Abstract
The genetic evolution of HIV-1 from its progenitor virus SIV following cross-species transmission is not well understood. Here we simulated the SIVcpz initial transmission to humans using humanized mice and followed the viral evolution during serial passages lasting more than a year. All three SIVcpz progenitor viruses used, namely LB715 and MB897 (group M) as well as EK505 (group N) readily infected hu-mice resulting in chronic viremia. Viral loads increased progressively to higher set-points and the CD4+ T cell decline became more pronounced by the end of the second serial passage indicating viral adaptation and increased pathogenicity. Viral genomes sequenced at different time points revealed many non-synonymous variants not previously reported that occurred throughout the viral genome, including the gag, pol, env, and nef genes. These results shed light on the potential changes that the SIVcpz genome had undergone during the initial stages of human infection and subsequent spread.Entities:
Keywords: HIV-1 evolution from SIVcpz; SIV genetic changes toward HIV-1; SIV pathogenesis in humanized mice; SIVcpz evolution into HIV-1; cross-species viral transmission; modeling SIV evolution into HIV using humanized mice; origin of human pathogens in NHP; viral adaptive changes and genetic evolution
Year: 2020 PMID: 32849468 PMCID: PMC7432304 DOI: 10.3389/fmicb.2020.01889
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 5.640