4.6 Article

High Prevalence of Simian Immunodeficiency Virus Infection in a Community of Savanna Chimpanzees

Journal

JOURNAL OF VIROLOGY
Volume 85, Issue 19, Pages 9918-9928

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.05475-11

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Funding

  1. National Institutes of Health [R01 AI50529, R01 AI58715]
  2. UAB Center for AIDS Research [P30 AI 27767]
  3. National Science Foundation (DDIG)
  4. Margot Marsh Biodiversity Foundation
  5. Department of Anthropology at the University of Texas at San Antonio
  6. Ruggles-Gates Fund for Biological Anthropology
  7. University of California in San Diego (UCSD COR)
  8. Carnegie Trust for Universities of Scotland
  9. Harold Hyam Wingate Foundation
  10. L. S. B. Leakey Foundation
  11. International Primatological Society
  12. Wenner Gren Foundation
  13. Howard Hughes Medical Institute

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Simian immunodeficiency virus of chimpanzees (SIVcpz) has a significant negative impact on the health, reproduction, and life span of chimpanzees, yet the prevalence and distribution of this virus in wild-living populations are still only poorly understood. Here, we show that savanna chimpanzees, who live in ecologically marginal habitats at 10- to 50-fold lower population densities than forest chimpanzees, can be infected with SIVcpz at high prevalence rates. Fecal samples were collected from nonhabituated eastern chimpanzees (Pan troglodytes schweinfurthii) in the Issa Valley (n = 375) and Shangwa River (n = 6) areas of the Masito-Ugalla region in western Tanzania, genotyped to determine the number of sampled individuals, and tested for SIVcpz-specific antibodies and nucleic acids. None of 5 Shangwa River apes tested positive for SIVcpz; however, 21 of 67 Issa Valley chimpanzees were SIVcpz infected, indicating a prevalence rate of 31% (95% confidence interval, 21% to 44%). Two individuals became infected during the 14-month observation period, documenting continuing virus spread in this community. To characterize the newly identified SIVcpz strains, partial and full-length viral sequences were amplified from fecal RNA of 10 infected chimpanzees. Phylogenetic analyses showed that the Ugalla viruses formed a monophyletic lineage most closely related to viruses endemic in Gombe National Park, also located in Tanzania, indicating a connection between these now separated communities at some time in the past. These findings document that SIVcpz is more widespread in Tanzania than previously thought and that even very low-density chimpanzee populations can be infected with SIVcpz at high prevalence rates. Determining whether savanna chimpanzees, who face much more extreme environmental conditions than forest chimpanzees, are more susceptible to SIVcpz-associated morbidity and mortality will have important scientific and conservation implications.

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