Biological signature characteristics of primary isolates from human immunodeficiency virus type 1 group O in ex vivo human tonsil histocultures

J Virol. 2009 Oct;83(20):10494-503. doi: 10.1128/JVI.00928-09. Epub 2009 Aug 12.

Abstract

Human immunodeficiency virus type 1 (HIV-1) group M viruses have achieved a global distribution, while HIV-1 group O viruses are endemic only in particular regions of Africa. Here, we evaluated biological characteristics of group O and group M viruses in ex vivo models of HIV-1 infection. The replicative capacity and ability to induce CD4 T-cell depletion of eight group O and seven group M primary isolates were monitored in cultures of human peripheral blood mononuclear cells and tonsil explants. Comparative and longitudinal infection studies revealed HIV-1 group-specific activity patterns: CCR5-using (R5) viruses from group M varied considerably in their replicative capacity but showed similar levels of cytopathicity. In contrast, R5 isolates from group O were relatively uniform in their replicative fitness but displayed a high and unprecedented variability in their potential to deplete CD4 T cells. Two R5 group O isolates were identified that cause massive depletion of CD4 T cells, to an extent comparable to CXCR4-using viruses and not documented for any R5 isolate from group M. Intergroup comparisons found a five- to eightfold lower replicative fitness of isolates from group O than for isolates from group M yet a similar overall intrinsic pathogenicity in tonsil cultures. This study establishes biological ex vivo characteristics of HIV-1 group O primary isolates. The current findings challenge the belief that a grossly reduced replicative fitness or inherently impaired cytopathicity of viruses from this group underlies their low global prevalence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD4-Positive T-Lymphocytes / immunology
  • Cell Line
  • Cells, Cultured
  • Cytopathogenic Effect, Viral
  • HIV-1 / classification*
  • HIV-1 / isolation & purification
  • HIV-1 / pathogenicity*
  • HIV-1 / physiology
  • Humans
  • Leukocytes, Mononuclear / virology*
  • Lymphocyte Activation
  • Organ Culture Techniques
  • Palatine Tonsil / cytology
  • Palatine Tonsil / immunology
  • Palatine Tonsil / virology*
  • Receptors, CCR5 / metabolism
  • Virus Replication

Substances

  • Receptors, CCR5