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A highly pathogenic simian/human immunodeficiency virus with genetic changes in cynomolgus monkey

Insights

A new simian/human immunodeficiency virus (SHIV-C2/1) causes rapid CD4+ lymphocyte depletion in monkeys. Pathogenicity may link to absent anti-Gag antibodies and specific genetic changes in the virus.

Area of Science:

  • Virology
  • Immunology
  • Primate Models

Background:

  • Simian/human immunodeficiency virus (SHIV) is a model for human immunodeficiency virus (HIV) research.
  • Understanding SHIV pathogenicity is crucial for developing effective HIV therapies.

Purpose of the Study:

  • To characterize a highly pathogenic SHIV strain (SHIV-C2/1) in cynomolgus monkeys.
  • To investigate the relationship between antibody response and SHIV pathogenicity.

Main Methods:

  • Infection of cynomolgus monkeys with SHIV-C2/1, p-SHIV, or SHIV-MN.
  • Monitoring of CD4+ lymphocyte counts, viral load, and antibody responses (anti-Gag, anti-Env).
  • Genetic sequencing of SHIV env and Nef genes.

Main Results:

  • SHIV-C2/1 induced rapid CD4+ depletion, diarrhea, and intense viremia within one week.
  • Anti-Gag antibody response was absent in SHIV-C2/1 infected animals, unlike p-SHIV or SHIV-MN infections.
  • Conserved genetic changes were identified in Env (C2, V3, gp41) and Nef proteins of pathogenic SHIV-C strains.

Conclusions:

  • The SHIV-C2/1-monkey model demonstrates rapid and severe pathogenicity.
  • Absence of anti-Gag antibody response may be associated with SHIV pathogenicity.
  • In vivo genetic alterations during serum passage contribute to SHIV virulence.

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