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Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees

Identifying microbial pathogens with zoonotic potential in wild-living primates can be important to human health, as evidenced by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) and Ebola virus. Simian foamy viruses (SFVs) are ancient retroviruses that infect Old and New World monkeys...

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Autores principales: Liu, Weimin, Worobey, Michael, Li, Yingying, Keele, Brandon F., Bibollet-Ruche, Frederic, Guo, Yuanyuan, Goepfert, Paul A., Santiago, Mario L., Ndjango, Jean-Bosco N., Neel, Cecile, Clifford, Stephen L., Sanz, Crickette, Kamenya, Shadrack, Wilson, Michael L., Pusey, Anne E., Gross-Camp, Nicole, Boesch, Christophe, Smith, Vince, Zamma, Koichiro, Huffman, Michael A., Mitani, John C., Watts, David P., Peeters, Martine, Shaw, George M., Switzer, William M., Sharp, Paul M., Hahn, Beatrice H.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435277/
https://www.ncbi.nlm.nih.gov/pubmed/18604273
http://dx.doi.org/10.1371/journal.ppat.1000097
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author Liu, Weimin
Worobey, Michael
Li, Yingying
Keele, Brandon F.
Bibollet-Ruche, Frederic
Guo, Yuanyuan
Goepfert, Paul A.
Santiago, Mario L.
Ndjango, Jean-Bosco N.
Neel, Cecile
Clifford, Stephen L.
Sanz, Crickette
Kamenya, Shadrack
Wilson, Michael L.
Pusey, Anne E.
Gross-Camp, Nicole
Boesch, Christophe
Smith, Vince
Zamma, Koichiro
Huffman, Michael A.
Mitani, John C.
Watts, David P.
Peeters, Martine
Shaw, George M.
Switzer, William M.
Sharp, Paul M.
Hahn, Beatrice H.
author_facet Liu, Weimin
Worobey, Michael
Li, Yingying
Keele, Brandon F.
Bibollet-Ruche, Frederic
Guo, Yuanyuan
Goepfert, Paul A.
Santiago, Mario L.
Ndjango, Jean-Bosco N.
Neel, Cecile
Clifford, Stephen L.
Sanz, Crickette
Kamenya, Shadrack
Wilson, Michael L.
Pusey, Anne E.
Gross-Camp, Nicole
Boesch, Christophe
Smith, Vince
Zamma, Koichiro
Huffman, Michael A.
Mitani, John C.
Watts, David P.
Peeters, Martine
Shaw, George M.
Switzer, William M.
Sharp, Paul M.
Hahn, Beatrice H.
author_sort Liu, Weimin
collection PubMed
description Identifying microbial pathogens with zoonotic potential in wild-living primates can be important to human health, as evidenced by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) and Ebola virus. Simian foamy viruses (SFVs) are ancient retroviruses that infect Old and New World monkeys and apes. Although not known to cause disease, these viruses are of public health interest because they have the potential to infect humans and thus provide a more general indication of zoonotic exposure risks. Surprisingly, no information exists concerning the prevalence, geographic distribution, and genetic diversity of SFVs in wild-living monkeys and apes. Here, we report the first comprehensive survey of SFVcpz infection in free-ranging chimpanzees (Pan troglodytes) using newly developed, fecal-based assays. Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706) or viral nucleic acids (n = 392). SFVcpz infection was documented at all field sites, with prevalence rates ranging from 44% to 100%. In two habituated communities, adult chimpanzees had significantly higher SFVcpz infection rates than infants and juveniles, indicating predominantly horizontal rather than vertical transmission routes. Some chimpanzees were co-infected with simian immunodeficiency virus (SIVcpz); however, there was no evidence that SFVcpz and SIVcpz were epidemiologically linked. SFVcpz nucleic acids were recovered from 177 fecal samples, all of which contained SFVcpz RNA and not DNA. Phylogenetic analysis of partial gag (616 bp), pol-RT (717 bp), and pol-IN (425 bp) sequences identified a diverse group of viruses, which could be subdivided into four distinct SFVcpz lineages according to their chimpanzee subspecies of origin. Within these lineages, there was evidence of frequent superinfection and viral recombination. One chimpanzee was infected by a foamy virus from a Cercopithecus monkey species, indicating cross-species transmission of SFVs in the wild. These data indicate that SFVcpz (i) is widely distributed among all chimpanzee subspecies; (ii) is shed in fecal samples as viral RNA; (iii) is transmitted predominantly by horizontal routes; (iv) is prone to superinfection and recombination; (v) has co-evolved with its natural host; and (vi) represents a sensitive marker of population structure that may be useful for chimpanzee taxonomy and conservation strategies.
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spelling pubmed-24352772008-07-04 Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees Liu, Weimin Worobey, Michael Li, Yingying Keele, Brandon F. Bibollet-Ruche, Frederic Guo, Yuanyuan Goepfert, Paul A. Santiago, Mario L. Ndjango, Jean-Bosco N. Neel, Cecile Clifford, Stephen L. Sanz, Crickette Kamenya, Shadrack Wilson, Michael L. Pusey, Anne E. Gross-Camp, Nicole Boesch, Christophe Smith, Vince Zamma, Koichiro Huffman, Michael A. Mitani, John C. Watts, David P. Peeters, Martine Shaw, George M. Switzer, William M. Sharp, Paul M. Hahn, Beatrice H. PLoS Pathog Research Article Identifying microbial pathogens with zoonotic potential in wild-living primates can be important to human health, as evidenced by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) and Ebola virus. Simian foamy viruses (SFVs) are ancient retroviruses that infect Old and New World monkeys and apes. Although not known to cause disease, these viruses are of public health interest because they have the potential to infect humans and thus provide a more general indication of zoonotic exposure risks. Surprisingly, no information exists concerning the prevalence, geographic distribution, and genetic diversity of SFVs in wild-living monkeys and apes. Here, we report the first comprehensive survey of SFVcpz infection in free-ranging chimpanzees (Pan troglodytes) using newly developed, fecal-based assays. Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpz-specific antibodies (n = 706) or viral nucleic acids (n = 392). SFVcpz infection was documented at all field sites, with prevalence rates ranging from 44% to 100%. In two habituated communities, adult chimpanzees had significantly higher SFVcpz infection rates than infants and juveniles, indicating predominantly horizontal rather than vertical transmission routes. Some chimpanzees were co-infected with simian immunodeficiency virus (SIVcpz); however, there was no evidence that SFVcpz and SIVcpz were epidemiologically linked. SFVcpz nucleic acids were recovered from 177 fecal samples, all of which contained SFVcpz RNA and not DNA. Phylogenetic analysis of partial gag (616 bp), pol-RT (717 bp), and pol-IN (425 bp) sequences identified a diverse group of viruses, which could be subdivided into four distinct SFVcpz lineages according to their chimpanzee subspecies of origin. Within these lineages, there was evidence of frequent superinfection and viral recombination. One chimpanzee was infected by a foamy virus from a Cercopithecus monkey species, indicating cross-species transmission of SFVs in the wild. These data indicate that SFVcpz (i) is widely distributed among all chimpanzee subspecies; (ii) is shed in fecal samples as viral RNA; (iii) is transmitted predominantly by horizontal routes; (iv) is prone to superinfection and recombination; (v) has co-evolved with its natural host; and (vi) represents a sensitive marker of population structure that may be useful for chimpanzee taxonomy and conservation strategies. Public Library of Science 2008-07-04 /pmc/articles/PMC2435277/ /pubmed/18604273 http://dx.doi.org/10.1371/journal.ppat.1000097 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Liu, Weimin
Worobey, Michael
Li, Yingying
Keele, Brandon F.
Bibollet-Ruche, Frederic
Guo, Yuanyuan
Goepfert, Paul A.
Santiago, Mario L.
Ndjango, Jean-Bosco N.
Neel, Cecile
Clifford, Stephen L.
Sanz, Crickette
Kamenya, Shadrack
Wilson, Michael L.
Pusey, Anne E.
Gross-Camp, Nicole
Boesch, Christophe
Smith, Vince
Zamma, Koichiro
Huffman, Michael A.
Mitani, John C.
Watts, David P.
Peeters, Martine
Shaw, George M.
Switzer, William M.
Sharp, Paul M.
Hahn, Beatrice H.
Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title_full Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title_fullStr Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title_full_unstemmed Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title_short Molecular Ecology and Natural History of Simian Foamy Virus Infection in Wild-Living Chimpanzees
title_sort molecular ecology and natural history of simian foamy virus infection in wild-living chimpanzees
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2435277/
https://www.ncbi.nlm.nih.gov/pubmed/18604273
http://dx.doi.org/10.1371/journal.ppat.1000097
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