Previous Article | Next Article 
Journal of Virology, October 2005, p. 12515-12527, Vol. 79, No. 19
0022-538X/05/$08.00+0 doi:10.1128/JVI.79.19.12515-12527.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Simian Immunodeficiency Virus Infection in Free-Ranging Sooty Mangabeys (Cercocebus atys atys) from the Taï Forest, Côte d'Ivoire: Implications for the Origin of Epidemic Human Immunodeficiency Virus Type 2
Mario L. Santiago,1,
Friederike Range,2,
Brandon F. Keele,1
Yingying Li,1
Elizabeth Bailes,3
Frederic Bibollet-Ruche,1
Cecile Fruteau,4
Ronald Noë,4
Martine Peeters,5
John F. Y. Brookfield,3
George M. Shaw,1,6
Paul M. Sharp,3 and
Beatrice H. Hahn1*
Departments of Medicine and Microbiology, University of Alabama at Birmingham,1
Howard Hughes Medical Institute, Birmingham, Alabama 35294,6
Department of Psychology, University of Pennsylvania, Philadelphia, Pennsylvania 19104,2
Institute of Genetics, University of Nottingham, Queens Medical Centre, Nottingham NH7 2UH, United Kingdom,3
Ethologie des Primates, Centre Ecologie, Physiologie et Ethologie (CNRS UPR 9010) and Université Louis Pasteur, Strasbourg, France,4
Laboratoire Retrovirus, UMR036, Institut de Recherche pour le Developement and Department of International Health, University of Montpellier I, Montpellier, France5
Received 9 June 2005/
Accepted 11 July 2005
Simian immunodeficiency virus of sooty mangabeys (SIVsmm) is recognized as the progenitor of human immunodeficiency virus type 2 (HIV-2) and has been transmitted to humans on multiple occasions, yet the epidemiology and genetic diversity of SIVsmm infection in wild-living populations remain largely unknown. Here, we report the first molecular epidemiological survey of SIVsmm in a community of
120 free-ranging sooty mangabeys in the Taï Forest, Côte d'Ivoire. Fecal samples (n = 39) were collected from 35 habituated animals (27 females and 8 males) and tested for SIVsmm virion RNA (vRNA). Viral gag (800 bp) and/or env (490 bp) sequences were amplified from 11 different individuals (eight females and three males). Based on the sensitivity of fecal vRNA detection and the numbers of samples analyzed, the prevalence of SIVsmm infection was estimated to be 59% (95% confidence interval, 0.35 to 0.88). Behavioral data collected from this community indicated that SIVsmm infection occurred preferentially in high-ranking females. Phylogenetic analysis of gag and env sequences revealed an extraordinary degree of genetic diversity, including evidence for frequent recombination events in both the recent and distant past. Some sooty mangabeys harbored near-identical viruses (<2% interstrain distance), indicating epidemiologically linked infections. These transmissions were identified by microsatellite analyses to involve both related (mother/daughter) and unrelated individuals, thus providing evidence for vertical and horizontal transmission in the wild. Finally, evolutionary tree analyses revealed significant clustering of the Taï SIVsmm strains with five of the eight recognized groups of HIV-2, including the epidemic groups A and B, thus pointing to a likely geographic origin of these human infections in the eastern part of the sooty mangabey range.
* Corresponding author. Mailing address: Department of Medicine, University of Alabama at Birmingham, 720 20th St. South, Kaul 816, Birmingham, AL 35294. Phone: (205) 934-0412. Fax: (205) 934-1580. E-mail:
bhahn{at}uab.edu.
Present address: Gladstone Institute of Virology and Immunology, University of California at San Francisco, 1650 Owens Street, San Francisco, CA 94158.
Present address: Department für Verhaltens-, Neuro- und Kognitions-Biologie, Universität Wien, Althanstrasse 14, A-1091 Vienna, Austria.
Journal of Virology, October 2005, p. 12515-12527, Vol. 79, No. 19
0022-538X/05/$08.00+0 doi:10.1128/JVI.79.19.12515-12527.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Ntemgwa, M. L., Toni, T. d., Brenner, B. G., Camacho, R. J., Wainberg, M. A.
(2009). Antiretroviral Drug Resistance in Human Immunodeficiency Virus Type 2. Antimicrob. Agents Chemother.
53: 3611-3619
[Full Text]
-
Takehisa, J., Kraus, M. H., Ayouba, A., Bailes, E., Van Heuverswyn, F., Decker, J. M., Li, Y., Rudicell, R. S., Learn, G. H., Neel, C., Ngole, E. M., Shaw, G. M., Peeters, M., Sharp, P. M., Hahn, B. H.
(2009). Origin and Biology of Simian Immunodeficiency Virus in Wild-Living Western Gorillas. J. Virol.
83: 1635-1648
[Abstract]
[Full Text]
-
Liegeois, F., Lafay, B., Formenty, P., Locatelli, S., Courgnaud, V., Delaporte, E., Peeters, M.
(2009). Full-Length Genome Characterization of a Novel Simian Immunodeficiency Virus Lineage (SIVolc) from Olive Colobus (Procolobus verus) and New SIVwrcPbb Strains from Western Red Colobus (Piliocolobus badius badius) from the Tai Forest in Ivory Coast. J. Virol.
83: 428-439
[Abstract]
[Full Text]
-
Parrish, C. R., Holmes, E. C., Morens, D. M., Park, E.-C., Burke, D. S., Calisher, C. H., Laughlin, C. A., Saif, L. J., Daszak, P.
(2008). Cross-Species Virus Transmission and the Emergence of New Epidemic Diseases. Microbiol. Mol. Biol. Rev.
72: 457-470
[Abstract]
[Full Text]
-
Pandrea, I., Onanga, R., Souquiere, S., Mouinga-Ondeme, A., Bourry, O., Makuwa, M., Rouquet, P., Silvestri, G., Simon, F., Roques, P., Apetrei, C.
(2008). Paucity of CD4+ CCR5+ T Cells May Prevent Transmission of Simian Immunodeficiency Virus in Natural Nonhuman Primate Hosts by Breast-Feeding. J. Virol.
82: 5501-5509
[Abstract]
[Full Text]
-
Wain, L. V., Bailes, E., Bibollet-Ruche, F., Decker, J. M., Keele, B. F., Van Heuverswyn, F., Li, Y., Takehisa, J., Ngole, E. M., Shaw, G. M., Peeters, M., Hahn, B. H., Sharp, P. M.
(2007). Adaptation of HIV-1 to Its Human Host. Mol Biol Evol
24: 1853-1860
[Abstract]
[Full Text]
-
Takehisa, J., Kraus, M. H., Decker, J. M., Li, Y., Keele, B. F., Bibollet-Ruche, F., Zammit, K. P., Weng, Z., Santiago, M. L., Kamenya, S., Wilson, M. L., Pusey, A. E., Bailes, E., Sharp, P. M., Shaw, G. M., Hahn, B. H.
(2007). Generation of Infectious Molecular Clones of Simian Immunodeficiency Virus from Fecal Consensus Sequences of Wild Chimpanzees. J. Virol.
81: 7463-7475
[Abstract]
[Full Text]
-
Cervasi, B., Paiardini, M., Serafini, S., Fraternale, A., Menotta, M., Engram, J., Lawson, B., Staprans, S. I., Piedimonte, G., Perno, C. F., Silvestri, G., Magnani, M.
(2006). Administration of Fludarabine-Loaded Autologous Red Blood Cells in Simian Immunodeficiency Virus-Infected Sooty Mangabeys Depletes pSTAT-1-Expressing Macrophages and Delays the Rebound of Viremia after Suspension of Antiretroviral Therapy.. J. Virol.
80: 10335-10345
[Abstract]
[Full Text]
-
VandeWoude, S., Apetrei, C.
(2006). Going Wild: Lessons from Naturally Occurring T-Lymphotropic Lentiviruses. Clin. Microbiol. Rev.
19: 728-762
[Abstract]
[Full Text]
-
Chen, J., Powell, D., Hu, W.-S.
(2006). High Frequency of Genetic Recombination Is a Common Feature of Primate Lentivirus Replication. J. Virol.
80: 9651-9658
[Abstract]
[Full Text]
-
Heeney, J. L., Dalgleish, A. G., Weiss, R. A.
(2006). Origins of HIV and the evolution of resistance to AIDS.. Science
313: 462-466
[Abstract]
[Full Text]
-
Keele, B. F., Van Heuverswyn, F., Li, Y., Bailes, E., Takehisa, J., Santiago, M. L., Bibollet-Ruche, F., Chen, Y., Wain, L. V., Liegeois, F., Loul, S., Ngole, E. M., Bienvenue, Y., Delaporte, E., Brookfield, J. F. Y., Sharp, P. M., Shaw, G. M., Peeters, M., Hahn, B. H.
(2006). Chimpanzee Reservoirs of Pandemic and Nonpandemic HIV-1. Science
313: 523-526
[Abstract]
[Full Text]