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Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study

The 2013–2016 Ebola virus outbreak in West Africa was the largest and deadliest outbreak to date. Here we conducted a serological study to examine the antibody levels in survivors and the seroconversion in close contacts who took care of Ebola-infected individuals, but did not develop symptoms of Eb...

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Autores principales: Halfmann, Peter J., Eisfeld, Amie J., Watanabe, Tokiko, Maemura, Tadashi, Yamashita, Makoto, Fukuyama, Satoshi, Armbrust, Tammy, Rozich, Isaiah, N’jai, Alhaji, Neumann, Gabriele, Kawaoka, Yoshihiro, Sahr, Foday
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692041/
https://www.ncbi.nlm.nih.gov/pubmed/31369554
http://dx.doi.org/10.1371/journal.pntd.0007654
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author Halfmann, Peter J.
Eisfeld, Amie J.
Watanabe, Tokiko
Maemura, Tadashi
Yamashita, Makoto
Fukuyama, Satoshi
Armbrust, Tammy
Rozich, Isaiah
N’jai, Alhaji
Neumann, Gabriele
Kawaoka, Yoshihiro
Sahr, Foday
author_facet Halfmann, Peter J.
Eisfeld, Amie J.
Watanabe, Tokiko
Maemura, Tadashi
Yamashita, Makoto
Fukuyama, Satoshi
Armbrust, Tammy
Rozich, Isaiah
N’jai, Alhaji
Neumann, Gabriele
Kawaoka, Yoshihiro
Sahr, Foday
author_sort Halfmann, Peter J.
collection PubMed
description The 2013–2016 Ebola virus outbreak in West Africa was the largest and deadliest outbreak to date. Here we conducted a serological study to examine the antibody levels in survivors and the seroconversion in close contacts who took care of Ebola-infected individuals, but did not develop symptoms of Ebola virus disease. In March 2017, we collected blood samples from 481 individuals in Makeni, Sierra Leone: 214 survivors and 267 close contacts. Using commercial, quantitative ELISAs, we tested the plasma for IgG-specific antibodies against three major viral antigens: GP, the only viral glycoprotein expressed on the virus surface; NP, the most abundant viral protein; and VP40, a major structural protein of Zaire ebolavirus. We also determined neutralizing antibody titers. In the cohort of Ebola survivors, 97.7% of samples (209/214) had measurable antibody levels against GP, NP, and/or VP40. Of these positive samples, all but one had measurable neutralizing antibody titers against Ebola virus. For the close contacts, up to 12.7% (34/267) may have experienced a subclinical virus infection as indicated by detectable antibodies against GP. Further investigation is warranted to determine whether these close contacts truly experienced subclinical infections and whether these asymptomatic infections played a role in the dynamics of transmission.
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spelling pubmed-66920412019-08-30 Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study Halfmann, Peter J. Eisfeld, Amie J. Watanabe, Tokiko Maemura, Tadashi Yamashita, Makoto Fukuyama, Satoshi Armbrust, Tammy Rozich, Isaiah N’jai, Alhaji Neumann, Gabriele Kawaoka, Yoshihiro Sahr, Foday PLoS Negl Trop Dis Research Article The 2013–2016 Ebola virus outbreak in West Africa was the largest and deadliest outbreak to date. Here we conducted a serological study to examine the antibody levels in survivors and the seroconversion in close contacts who took care of Ebola-infected individuals, but did not develop symptoms of Ebola virus disease. In March 2017, we collected blood samples from 481 individuals in Makeni, Sierra Leone: 214 survivors and 267 close contacts. Using commercial, quantitative ELISAs, we tested the plasma for IgG-specific antibodies against three major viral antigens: GP, the only viral glycoprotein expressed on the virus surface; NP, the most abundant viral protein; and VP40, a major structural protein of Zaire ebolavirus. We also determined neutralizing antibody titers. In the cohort of Ebola survivors, 97.7% of samples (209/214) had measurable antibody levels against GP, NP, and/or VP40. Of these positive samples, all but one had measurable neutralizing antibody titers against Ebola virus. For the close contacts, up to 12.7% (34/267) may have experienced a subclinical virus infection as indicated by detectable antibodies against GP. Further investigation is warranted to determine whether these close contacts truly experienced subclinical infections and whether these asymptomatic infections played a role in the dynamics of transmission. Public Library of Science 2019-08-01 /pmc/articles/PMC6692041/ /pubmed/31369554 http://dx.doi.org/10.1371/journal.pntd.0007654 Text en © 2019 Halfmann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Halfmann, Peter J.
Eisfeld, Amie J.
Watanabe, Tokiko
Maemura, Tadashi
Yamashita, Makoto
Fukuyama, Satoshi
Armbrust, Tammy
Rozich, Isaiah
N’jai, Alhaji
Neumann, Gabriele
Kawaoka, Yoshihiro
Sahr, Foday
Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title_full Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title_fullStr Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title_full_unstemmed Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title_short Serological analysis of Ebola virus survivors and close contacts in Sierra Leone: A cross-sectional study
title_sort serological analysis of ebola virus survivors and close contacts in sierra leone: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692041/
https://www.ncbi.nlm.nih.gov/pubmed/31369554
http://dx.doi.org/10.1371/journal.pntd.0007654
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