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SIV/SHIV-Zika co-infection does not alter disease pathogenesis in adult non-pregnant rhesus macaque model.

Mehdi R M BidokhtiDebashis DuttaLepakshe S V MadduriShawna M WoollardRobert NorgrenLuis GiavedoniSiddappa N Byrareddy
Published in: PLoS neglected tropical diseases (2018)
Due to the large geographical overlap of populations exposed to Zika virus (ZIKV) and human immunodeficiency virus (HIV), understanding the disease pathogenesis of co-infection is urgently needed. This warrants the development of an animal model for HIV-ZIKV co-infection. In this study, we used adult non-pregnant macaques that were chronically infected with simian immunodeficiency virus/chimeric simian human immunodeficiency virus (SIV/SHIV) and then inoculated with ZIKV. Plasma viral loads of both SIV/SHIV and ZIKV co-infected animals revealed no significant changes as compared to animals that were infected with ZIKV alone or as compared to SIV/SHIV infected animals prior to ZIKV inoculation. ZIKV tissue clearance of co-infected animals was similar to animals that were infected with ZIKV alone. Furthermore, in co-infected macaques, there was no statistically significant difference in plasma cytokines/chemokines levels as compared to prior to ZIKV inoculation. Collectively, these findings suggest that co-infection may not alter disease pathogenesis, thus warranting larger HIV-ZIKV epidemiological studies in order to validate these findings.
Keyphrases
  • zika virus
  • human immunodeficiency virus
  • antiretroviral therapy
  • hepatitis c virus
  • dengue virus
  • hiv infected
  • hiv positive
  • aedes aegypti
  • hiv aids
  • pregnant women
  • stem cells
  • mesenchymal stem cells
  • bone marrow