4.4 Article

Modeling the evolution of SIV sooty mangabey progenitor virus towards HIV-2 using humanized mice

Journal

VIROLOGY
Volume 510, Issue -, Pages 175-184

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2017.07.005

Keywords

SIVsm evolution into HIV-2 lineage; Modeling SW evolution into HIV in humanized mice; SIV pathogenesis in humanized mice; SIV genetic changes towards HW-2; Origin of human pathogens in NHP; Viral adaptive changes and genetic evolution; Cross-species viral transmission

Categories

Funding

  1. NIH, USA [RO1 AI12334]
  2. National Center for Research Resources
  3. Office of Research Infrastructure Programs (ORIP) of the NIH at the Tulane National Primate Research Center [OD011104]
  4. NIH at the Wisconsin National Primate Research Center [P51OD011106]

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HIV-2 is thought to have originated from an SIV progenitor native to sooty mangabeys. To model the initial human transmission and understand the sequential viral evolution, humanized mice were infected with SIVsm and serially passaged for five generations. Productive infection was seen by week 3 during the initial challenge followed by chronic viremia and gradual CD4(+) T cell decline. Viral loads increased by the 5th generation resulting in more rapid CD4(+) T cell decline. Genetic analysis revealed several amino acid substitutions that were nonsynonymous and fixed in multiple hu-mice across each of the 5 generations in the nef, env and rev regions. The highest rate of substitution occurred in the nef and env regions and most were observed within the first two generations. These data demonstrated the utility of hu-mice in modeling the SIVsm transmission to the human and to evaluate its potential sequential evolution into a human pathogen of HW-2 lineage.

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