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Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo
BACKGROUND: Ebola virus (EBOV) is a zoonotic filovirus spread through exposure to infected bodily fluids of a human or animal. Though EBOV is capable of causing severe disease, referred to as Ebola Virus Disease (EVD), individuals who have never been diagnosed with confirmed, probable or suspected E...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384205/ https://www.ncbi.nlm.nih.gov/pubmed/34383755 http://dx.doi.org/10.1371/journal.pntd.0009566 |
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author | Bratcher, Anna Hoff, Nicole A. Doshi, Reena H. Gadoth, Adva Halbrook, Megan Mukadi, Patrick Musene, Kamy Ilunga-Kebela, Benoit Spencer, D’Andre Bramble, Matthew S. McIlwan, David Kelly, J. Daniel Mukadi, Daniel Kingebeni, Placide Mbala Ahuka, Steve Okitolonda-Wemakoy, Emile Muyembe-Tamfum, Jean-Jacques Rimoin, Anne W. |
author_facet | Bratcher, Anna Hoff, Nicole A. Doshi, Reena H. Gadoth, Adva Halbrook, Megan Mukadi, Patrick Musene, Kamy Ilunga-Kebela, Benoit Spencer, D’Andre Bramble, Matthew S. McIlwan, David Kelly, J. Daniel Mukadi, Daniel Kingebeni, Placide Mbala Ahuka, Steve Okitolonda-Wemakoy, Emile Muyembe-Tamfum, Jean-Jacques Rimoin, Anne W. |
author_sort | Bratcher, Anna |
collection | PubMed |
description | BACKGROUND: Ebola virus (EBOV) is a zoonotic filovirus spread through exposure to infected bodily fluids of a human or animal. Though EBOV is capable of causing severe disease, referred to as Ebola Virus Disease (EVD), individuals who have never been diagnosed with confirmed, probable or suspected EVD can have detectable EBOV antigen-specific antibodies in their blood. This study aims to identify risk factors associated with detectable antibody levels in the absence of an EVD diagnosis. METHODOLOGY: Data was collected from September 2015 to August 2017 from 1,366 consenting individuals across four study sites in the DRC (Boende, Kabondo-Dianda, Kikwit, and Yambuku). Seroreactivity was determined to EBOV GP IgG using Zaire Ebola Virus Glycoprotein (EBOV GP antigen) ELISA kits (Alpha Diagnostic International, Inc.) in Kinshasa, DRC; any result above 4.7 units/mL was considered seroreactive. Among the respondents, 113 (8.3%) were considered seroreactive. Several zoonotic exposures were associated with EBOV seroreactivity after controlling for age, sex, healthcare worker status, location, and history of contact with an EVD case, namely: ever having contact with bats, ever having contact with rodents, and ever eating non-human primate meat. Contact with monkeys or non-human primates was not associated with seroreactivity. CONCLUSIONS: This analysis suggests that some zoonotic exposures that have been linked to EVD outbreaks can also be associated with EBOV GP seroreactivity in the absence of diagnosed EVD. Future investigations should seek to clarify the relationships between zoonotic exposures, seroreactivity, asymptomatic infection, and EVD. |
format | Online Article Text |
id | pubmed-8384205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83842052021-08-25 Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo Bratcher, Anna Hoff, Nicole A. Doshi, Reena H. Gadoth, Adva Halbrook, Megan Mukadi, Patrick Musene, Kamy Ilunga-Kebela, Benoit Spencer, D’Andre Bramble, Matthew S. McIlwan, David Kelly, J. Daniel Mukadi, Daniel Kingebeni, Placide Mbala Ahuka, Steve Okitolonda-Wemakoy, Emile Muyembe-Tamfum, Jean-Jacques Rimoin, Anne W. PLoS Negl Trop Dis Research Article BACKGROUND: Ebola virus (EBOV) is a zoonotic filovirus spread through exposure to infected bodily fluids of a human or animal. Though EBOV is capable of causing severe disease, referred to as Ebola Virus Disease (EVD), individuals who have never been diagnosed with confirmed, probable or suspected EVD can have detectable EBOV antigen-specific antibodies in their blood. This study aims to identify risk factors associated with detectable antibody levels in the absence of an EVD diagnosis. METHODOLOGY: Data was collected from September 2015 to August 2017 from 1,366 consenting individuals across four study sites in the DRC (Boende, Kabondo-Dianda, Kikwit, and Yambuku). Seroreactivity was determined to EBOV GP IgG using Zaire Ebola Virus Glycoprotein (EBOV GP antigen) ELISA kits (Alpha Diagnostic International, Inc.) in Kinshasa, DRC; any result above 4.7 units/mL was considered seroreactive. Among the respondents, 113 (8.3%) were considered seroreactive. Several zoonotic exposures were associated with EBOV seroreactivity after controlling for age, sex, healthcare worker status, location, and history of contact with an EVD case, namely: ever having contact with bats, ever having contact with rodents, and ever eating non-human primate meat. Contact with monkeys or non-human primates was not associated with seroreactivity. CONCLUSIONS: This analysis suggests that some zoonotic exposures that have been linked to EVD outbreaks can also be associated with EBOV GP seroreactivity in the absence of diagnosed EVD. Future investigations should seek to clarify the relationships between zoonotic exposures, seroreactivity, asymptomatic infection, and EVD. Public Library of Science 2021-08-12 /pmc/articles/PMC8384205/ /pubmed/34383755 http://dx.doi.org/10.1371/journal.pntd.0009566 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Bratcher, Anna Hoff, Nicole A. Doshi, Reena H. Gadoth, Adva Halbrook, Megan Mukadi, Patrick Musene, Kamy Ilunga-Kebela, Benoit Spencer, D’Andre Bramble, Matthew S. McIlwan, David Kelly, J. Daniel Mukadi, Daniel Kingebeni, Placide Mbala Ahuka, Steve Okitolonda-Wemakoy, Emile Muyembe-Tamfum, Jean-Jacques Rimoin, Anne W. Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title | Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title_full | Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title_fullStr | Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title_full_unstemmed | Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title_short | Zoonotic risk factors associated with seroprevalence of Ebola virus GP antibodies in the absence of diagnosed Ebola virus disease in the Democratic Republic of Congo |
title_sort | zoonotic risk factors associated with seroprevalence of ebola virus gp antibodies in the absence of diagnosed ebola virus disease in the democratic republic of congo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384205/ https://www.ncbi.nlm.nih.gov/pubmed/34383755 http://dx.doi.org/10.1371/journal.pntd.0009566 |
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