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A highly pathogenic simian/human immunodeficiency virus with genetic changes in cynomolgus monkey
Abstract:
A highly pathogenic simian/human immunodeficiency virus (SHIV), designated C2/1, was obtained by serum passages in cynomolgus monkeys of p-SHIV, an SHIV strain that contains the env gene of pathogenic human immunodeficiency virus type 1 89.6. CD4+ lymphocyte depletion was induced within 1 week of the SHIV-C2/1 infection in peripheral blood as well as in various lymphoid organs in all the animals tested, with symptoms of diarrhoea and no increase in body weight, followed by intense viraemia. Serum antibody against Env protein was detected from 4 weeks after the virus infection, while the anti-Gag antibody response was absent in the SHIV-C2/1-infected animals. In contrast, both anti-Gag and anti-Env antibody responses were present in animals infected with p-SHIV or the non-pathogenic SHIV-MN. Sequencing of the env gene of isolates of SHIV-C strains showed conserved amino acid changes in the Env C2 and V3 regions that included changes to negatively charged amino acids, in the cytoplasmic region of gp41 that included a 42 amino acid deletion, and in the Nef protein. The pathogenic SHIV-C2/1-monkey model suggests that virus-specific pathogenicity in SHIV infection may be associated with the absence of anti-Gag antibody responses in animals and may be caused by genetic changes during serum passage in vivo.
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.