Isolation and partial characterization of a lentivirus from talapoin monkeys (Myopithecus talapoin)

A D Osterhaus1, N Pedersen, G van Amerongen

  • 1Laboratory of Immunobiology, National Institute for Public Health and Environmental Protection, Bilthoven, The Netherlands.

Virology
|July 16, 1999
PubMed

Insights

Researchers discovered a new simian immunodeficiency virus (SIVtal) in talapoin monkeys. This novel lentivirus can infect other macaque species, causing seroconversion but minimal immunodeficiency.

Area of Science:

  • Virology
  • Primate Immunology
  • Infectious Diseases

Background:

  • Talapoin monkeys (Myopithecus talapoin) exhibit human immunodeficiency virus-1 cross-reactive antibodies.
  • Previous research suggested the presence of lentiviruses in this primate species.

Purpose of the Study:

  • To identify and characterize a novel lentivirus in talapoin monkeys.
  • To investigate the transmission and pathogenicity of this new virus in various primate models.

Main Methods:

  • Virus isolation from seropositive talapoin monkeys.
  • Propagation in primate peripheral blood mononuclear cells.
  • Experimental infection of talapoin, rhesus, and cynomolgus macaques.
  • PCR amplification and DNA sequencing of viral polymerase gene fragments.
  • Monitoring of CD4(+) cell counts in infected animals.

Main Results:

  • A novel simian immunodeficiency virus, SIVtal, was isolated and identified in talapoin monkeys.
  • SIVtal was transmissible between captive monkeys via unknown routes.
  • The virus could be propagated in talapoin monkey cells but not human cell lines.
  • Experimental infection of talapoin and macaque species resulted in seroconversion and viral reisolation.
  • Chronically infected talapoin monkeys showed a decrease in CD4(+) cells, but no other immunodeficiency signs were observed.
  • Genetic analysis indicated SIVtal is distinct from known lentiviruses, possibly related to SIV from Sykes monkeys.

Conclusions:

  • SIVtal represents a novel lentivirus in talapoin monkeys with potential for interspecies transmission.
  • While SIVtal causes CD4(+) cell reduction in chronically infected talapoins, its pathogenic potential appears limited in the short term.
  • Further research is needed to understand the evolutionary relationships and full pathogenic spectrum of SIVtal.

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