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Evidence for henipavirus spillover into human populations in Africa
Zoonotic transmission of lethal henipaviruses (HNVs) from their natural fruit bat reservoirs to humans has only been reported in Australia and South/Southeast Asia. However, a recent study discovered numerous HNV clades in African bat samples. To determine the potential for HNV spillover events amon...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237230/ https://www.ncbi.nlm.nih.gov/pubmed/25405640 http://dx.doi.org/10.1038/ncomms6342 |
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author | Pernet, Olivier Schneider, Bradley S. Beaty, Shannon M. LeBreton, Matthew Yun, Tatyana E. Park, Arnold Zachariah, Trevor T. Bowden, Thomas A. Hitchens, Peta Ramirez, Christina M. Daszak, Peter Mazet, Jonna Freiberg, Alexander N. Wolfe, Nathan D. Lee, Benhur |
author_facet | Pernet, Olivier Schneider, Bradley S. Beaty, Shannon M. LeBreton, Matthew Yun, Tatyana E. Park, Arnold Zachariah, Trevor T. Bowden, Thomas A. Hitchens, Peta Ramirez, Christina M. Daszak, Peter Mazet, Jonna Freiberg, Alexander N. Wolfe, Nathan D. Lee, Benhur |
author_sort | Pernet, Olivier |
collection | PubMed |
description | Zoonotic transmission of lethal henipaviruses (HNVs) from their natural fruit bat reservoirs to humans has only been reported in Australia and South/Southeast Asia. However, a recent study discovered numerous HNV clades in African bat samples. To determine the potential for HNV spillover events among humans in Africa, here we examine well-curated sets of bat (Eidolon helvum, n=44) and human (n=497) serum samples from Cameroon for Nipah virus (NiV) cross-neutralizing antibodies (NiV-X-Nabs). Using a vesicular stomatitis virus (VSV)-based pseudoparticle seroneutralization assay, we detect NiV-X-Nabs in 48% and 3–4% of the bat and human samples, respectively. Seropositive human samples are found almost exclusively in individuals who reported butchering bats for bushmeat. Seropositive human sera also neutralize Hendra virus and Gh-M74a (an African HNV) pseudoparticles, as well as live NiV. Butchering bat meat and living in areas undergoing deforestation are the most significant risk factors associated with seropositivity. Evidence for HNV spillover events warrants increased surveillance efforts. |
format | Online Article Text |
id | pubmed-4237230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42372302014-12-05 Evidence for henipavirus spillover into human populations in Africa Pernet, Olivier Schneider, Bradley S. Beaty, Shannon M. LeBreton, Matthew Yun, Tatyana E. Park, Arnold Zachariah, Trevor T. Bowden, Thomas A. Hitchens, Peta Ramirez, Christina M. Daszak, Peter Mazet, Jonna Freiberg, Alexander N. Wolfe, Nathan D. Lee, Benhur Nat Commun Article Zoonotic transmission of lethal henipaviruses (HNVs) from their natural fruit bat reservoirs to humans has only been reported in Australia and South/Southeast Asia. However, a recent study discovered numerous HNV clades in African bat samples. To determine the potential for HNV spillover events among humans in Africa, here we examine well-curated sets of bat (Eidolon helvum, n=44) and human (n=497) serum samples from Cameroon for Nipah virus (NiV) cross-neutralizing antibodies (NiV-X-Nabs). Using a vesicular stomatitis virus (VSV)-based pseudoparticle seroneutralization assay, we detect NiV-X-Nabs in 48% and 3–4% of the bat and human samples, respectively. Seropositive human samples are found almost exclusively in individuals who reported butchering bats for bushmeat. Seropositive human sera also neutralize Hendra virus and Gh-M74a (an African HNV) pseudoparticles, as well as live NiV. Butchering bat meat and living in areas undergoing deforestation are the most significant risk factors associated with seropositivity. Evidence for HNV spillover events warrants increased surveillance efforts. Nature Pub. Group 2014-11-18 /pmc/articles/PMC4237230/ /pubmed/25405640 http://dx.doi.org/10.1038/ncomms6342 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pernet, Olivier Schneider, Bradley S. Beaty, Shannon M. LeBreton, Matthew Yun, Tatyana E. Park, Arnold Zachariah, Trevor T. Bowden, Thomas A. Hitchens, Peta Ramirez, Christina M. Daszak, Peter Mazet, Jonna Freiberg, Alexander N. Wolfe, Nathan D. Lee, Benhur Evidence for henipavirus spillover into human populations in Africa |
title | Evidence for henipavirus spillover into human populations in Africa |
title_full | Evidence for henipavirus spillover into human populations in Africa |
title_fullStr | Evidence for henipavirus spillover into human populations in Africa |
title_full_unstemmed | Evidence for henipavirus spillover into human populations in Africa |
title_short | Evidence for henipavirus spillover into human populations in Africa |
title_sort | evidence for henipavirus spillover into human populations in africa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237230/ https://www.ncbi.nlm.nih.gov/pubmed/25405640 http://dx.doi.org/10.1038/ncomms6342 |
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