Capsid-dependent and -independent postentry restriction of primate lentivirus tropism in rodent cells

J Virol. 2004 Jan;78(2):1006-11. doi: 10.1128/jvi.78.2.1006-1011.2004.

Abstract

Retrovirus tropism can be restricted by cellular factors such as Fv1, Ref1, and Lv1 that inhibit infection by targeting the incoming viral capsid. Here, we show that rodent cells exhibit differential sensitivity to infection by vesicular stomatitis virus G-pseudotyped lentiviruses and that differences between human immunodeficiency virus type 1 and simian immunodeficiency virus (SIVmac) infectivity are sometimes, but not always, governed by determinants in capsid-p2. In at least one case, resistance to SIVmac infection could be eliminated by saturation of target cells with noninfectious SIVmac particles. However, cross-saturation experiments and analysis of Fv1-null cells engineered to express natural or artificial Fv1 proteins revealed that lentivirus restriction in mouse cells is independent of Fv1. Overall, these findings indicate that novel restriction factors in rodents can modulate sensitivity to specific primate lentiviruses.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Capsid / metabolism*
  • Cell Line
  • Green Fluorescent Proteins
  • HIV-1 / pathogenicity
  • HIV-1 / physiology
  • HIV-2 / pathogenicity
  • HIV-2 / physiology
  • Humans
  • Lentiviruses, Primate / pathogenicity*
  • Lentiviruses, Primate / physiology*
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred AKR
  • Mice, Inbred C57BL
  • NIH 3T3 Cells
  • Proteins / metabolism
  • Rodentia / virology*
  • Simian Immunodeficiency Virus / pathogenicity
  • Simian Immunodeficiency Virus / physiology
  • Viral Envelope Proteins / genetics
  • Viral Envelope Proteins / metabolism

Substances

  • Fv1 protein, mouse
  • G protein, vesicular stomatitis virus
  • Luminescent Proteins
  • Membrane Glycoproteins
  • Proteins
  • Viral Envelope Proteins
  • Green Fluorescent Proteins