Foci of endemic simian immunodeficiency virus infection in wild-living eastern chimpanzees (Pan troglodytes schweinfurthii)

被引:90
作者
Santiago, ML
Lukasik, M
Kamenya, S
Li, YY
Bibollet-Ruche, F
Bailes, E
Muller, MN
Emery, M
Goldenberg, DA
Lwanga, JS
Ayouba, A
Nerrienet, E
McClure, HM
Heeney, JL
Watts, DP
Pusey, AE
Collins, DA
Wrangham, RW
Goodall, J
Brookfield, JFY
Sharp, PM
Shaw, GM
Hahn, BH
机构
[1] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[3] Howard Hughes Med Inst, Birmingham, AL 35294 USA
[4] Jane Goodall Inst Tanzania, Gombe Stream Res Ctr, Kigoma, Tanzania
[5] Univ Nottingham, Inst Genet, Queens Med Ctr, Nottingham NH7 2UH, England
[6] Harvard Univ, Dept Anthropol, Cambridge, MA 02138 USA
[7] Yale Univ, Dept Anthropol, New Haven, CT 06520 USA
[8] Makerere Univ, Biol Field Stn, Kibale Natl Pk, Kampala, Uganda
[9] Ctr Pasteur Cameroun, Yaounde, Cameroon
[10] Yerkes Natl Primate Res Ctr, Div Res Resources, Atlanta, GA 30329 USA
[11] Biomed Primate Res Ctr, Dept Virol, Rijswijk, Netherlands
[12] Univ Minnesota, Dept Ecol Evolut & Behav, St Paul, MN 55108 USA
[13] Jane Goodall Inst, Silver Spring, MD 20911 USA
关键词
D O I
10.1128/JVI.77.13.7545-7562.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Simian immunodeficiency virus of chimpanzees (SlVcpz) is the immediate precursor to human immunodeficiency virus type 1 (HIV-1), yet remarkably, the distribution and prevalence of SlVcpz in wild ape populations are unknown. Studies of SlVcpz infection rates in wild chimpanzees are complicated by the species' endangered status and by its geographic location in remote areas of sub-Saharan Africa. We have developed sensitive and specific urine and fecal tests for SIVcpz antibody and virion RNA (vRNA) detection and describe herein the first comprehensive prevalence study of SIVcpz infection in five wild Pan troglodytes schweinfurthii communities in east Africa. In Kibale National Park in Uganda, 31 (of 52) members of the Kanyawara community and 39 (of similar to145) members of the Ngogo community were studied; none were found to be positive for SIVcpz infection. In Gombe National Park in Tanzania, 15 (of 20) members of the Mitumba community, 51 (of 55) members of the Kasekela community, and at least 10 (of similar to20) members of the Kalande community were studied. Seven individuals were SIVcpz antibody and/or vRNA positive, and two others had indeterminate antibody results. Based on assay sensitivities and the numbers and types of specimens analyzed, we estimated the prevalence of SIVcpz infection to be 17% in Mitumba (95% confidence interval, 10 to 40%), 5% in Kasekela (95% confidence interval, 4 to 7%), and 30% in Kalande (95% confidence interval, 15 to 60%). For Gombe as a whole, the SIVcpz prevalence was estimated to be 13% (95% confidence interval, 7 to 25%). SIVcpz infection was confirmed in five chimpanzees by PCR amplification of partial pot and gp41/nef sequences which revealed a diverse group of viruses that formed a monophyletic lineage within the SIVcpzPts radiation. Although none of the 70 Kibale chimpanzees tested SIVcpz positive, we estimated the likelihood that a 10% or higher prevalence existed but went undetected because of sampling and assay limitations; this possibility was ruled out with 95% certainty. These results indicate that SIVcpz is unevenly distributed among P. t. schweinfurthii in east Africa, with foci or "hot spots" of SlVcpz endemicity in some communities and rare or absent infection in others. This situation contrasts with that for smaller monkey species, in which infection rates by related SIVs are generally much higher and more uniform among different groups and populations. The basis for the wide variability in SIVcpz infection rates in east African apes and the important question of SIVcpz prevalence in west central African chimpanzees (Pan troglodytes troglodytes) remain to be elucidated.
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页码:7545 / 7562
页数:18
相关论文
共 62 条
[1]   SPECIES-SPECIFIC DIVERSITY AMONG SIMIAN IMMUNODEFICIENCY VIRUSES FROM AFRICAN-GREEN MONKEYS [J].
ALLAN, JS ;
SHORT, M ;
TAYLOR, ME ;
SU, S ;
HIRSCH, VM ;
JOHNSON, PR ;
SHAW, GM ;
HAHN, BH .
JOURNAL OF VIROLOGY, 1991, 65 (06) :2816-2828
[2]  
BAILES E, 2003, IN PRESS HYBRID ORIG
[3]  
BAILES E, 2002, MOL EPIDEMIOLOGY HUM, P65
[4]   Patterns of genomic sequence diversity among their simian immunodeficiency viruses suggest that L'Hoest monkeys (Cercopithecus lhoesti) are a natural lentivirus reservoir [J].
Beer, BE ;
Bailes, E ;
Dapolito, G ;
Campbell, BJ ;
Goeken, RM ;
Axthelm, MK ;
Markham, PD ;
Bernard, J ;
Zagury, D ;
Franchini, G ;
Sharp, PM ;
Hirsch, VM .
JOURNAL OF VIROLOGY, 2000, 74 (08) :3892-3898
[5]   Simian immunodeficiency virus infection in a patas monkey (Erythrocebus patas): Evidence for cross-species transmission from African green monkeys (Cercopithecus aethiops sabaeus) in the wild [J].
BibolletRuche, F ;
GalatLuong, A ;
Cuny, G ;
SarniManchado, P ;
Galat, G ;
Durand, JP ;
Pourrut, X ;
Veas, F .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :773-781
[6]   Characteristics of primary infection of a European human immunodeficiency virus type 1 clade B isolate in chimpanzees [J].
Bogers, WMJM ;
Koornstra, WH ;
Dubbes, RH ;
ten Haaft, PJF ;
Verstrepen, BE ;
Jhagjhoorsingh, SS ;
Haaksma, AGM ;
Niphuis, H ;
Laman, JD ;
Norley, S ;
Schuitemaker, H ;
Goudsmit, J ;
Hunsmann, G ;
Heeney, JL ;
Wigzell, H .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :2895-2903
[7]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[8]  
Butynski Thomas M., 2001, P3
[9]  
*CDCP, 1989, MMWR MORB MORTAL S8, V38, pS1
[10]  
Chakrabarti L, 2002, EMERGENCE OF ZOONOTIC DISEASES, WORKSHOP SUMMARY, P61