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Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey
INTRODUCTION: Evidence for minimally symptomatic Ebola virus (EBOV) infection is limited. During the 2013–16 outbreak in West Africa, it was not considered epidemiologically relevant to published models or projections of intervention effects. In order to improve our understanding of the transmission...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112953/ https://www.ncbi.nlm.nih.gov/pubmed/27846221 http://dx.doi.org/10.1371/journal.pntd.0005087 |
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author | Richardson, Eugene T. Kelly, J. Daniel Barrie, Mohamed Bailor Mesman, Annelies W. Karku, Sahr Quiwa, Komba Marsh, Regan H. Koedoyoma, Songor Daboh, Fodei Barron, Kathryn P. Grady, Michael Tucker, Elizabeth Dierberg, Kerry L. Rutherford, George W. Barry, Michele Jones, James Holland Murray, Megan B. Farmer, Paul E. |
author_facet | Richardson, Eugene T. Kelly, J. Daniel Barrie, Mohamed Bailor Mesman, Annelies W. Karku, Sahr Quiwa, Komba Marsh, Regan H. Koedoyoma, Songor Daboh, Fodei Barron, Kathryn P. Grady, Michael Tucker, Elizabeth Dierberg, Kerry L. Rutherford, George W. Barry, Michele Jones, James Holland Murray, Megan B. Farmer, Paul E. |
author_sort | Richardson, Eugene T. |
collection | PubMed |
description | INTRODUCTION: Evidence for minimally symptomatic Ebola virus (EBOV) infection is limited. During the 2013–16 outbreak in West Africa, it was not considered epidemiologically relevant to published models or projections of intervention effects. In order to improve our understanding of the transmission dynamics of EBOV in humans, we investigated the occurrence of minimally symptomatic EBOV infection in quarantined contacts of reported Ebola virus disease cases in a recognized ‘hotspot.’ METHODOLOGY/PRINCIPAL FINDINGS: We conducted a cross-sectional serosurvey in Sukudu, Kono District, Sierra Leone, from October 2015 to January 2016. A blood sample was collected from 187 study participants, 132 negative controls (individuals with a low likelihood of previous exposure to Ebola virus), and 30 positive controls (Ebola virus disease survivors). IgG responses to Ebola glycoprotein and nucleoprotein were measured using Alpha Diagnostic International ELISA kits with plasma diluted at 1:200. Optical density was read at 450 nm (subtracting OD at 630nm to normalize well background) on a ChroMate 4300 microplate reader. A cutoff of 4.7 U/mL for the anti-GP ELISA yielded 96.7% sensitivity and 97.7% specificity in distinguishing positive and negative controls. We identified 14 seropositive individuals not known to have had Ebola virus disease. Two of the 14 seropositive individuals reported only fever during quarantine while the remaining 12 denied any signs or symptoms during quarantine. CONCLUSIONS/SIGNIFICANCE: By using ELISA to measure Zaire Ebola virus antibody concentrations, we identified a significant number of individuals with previously undetected EBOV infection in a ‘hotspot’ village in Sierra Leone, approximately one year after the village outbreak. The findings provide further evidence that Ebola, like many other viral infections, presents with a spectrum of clinical manifestations, including minimally symptomatic infection. These data also suggest that a significant portion of Ebola transmission events may have gone undetected during the outbreak. Further studies are needed to understand the potential risk of transmission and clinical sequelae in individuals with previously undetected EBOV infection. |
format | Online Article Text |
id | pubmed-5112953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51129532016-12-08 Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey Richardson, Eugene T. Kelly, J. Daniel Barrie, Mohamed Bailor Mesman, Annelies W. Karku, Sahr Quiwa, Komba Marsh, Regan H. Koedoyoma, Songor Daboh, Fodei Barron, Kathryn P. Grady, Michael Tucker, Elizabeth Dierberg, Kerry L. Rutherford, George W. Barry, Michele Jones, James Holland Murray, Megan B. Farmer, Paul E. PLoS Negl Trop Dis Research Article INTRODUCTION: Evidence for minimally symptomatic Ebola virus (EBOV) infection is limited. During the 2013–16 outbreak in West Africa, it was not considered epidemiologically relevant to published models or projections of intervention effects. In order to improve our understanding of the transmission dynamics of EBOV in humans, we investigated the occurrence of minimally symptomatic EBOV infection in quarantined contacts of reported Ebola virus disease cases in a recognized ‘hotspot.’ METHODOLOGY/PRINCIPAL FINDINGS: We conducted a cross-sectional serosurvey in Sukudu, Kono District, Sierra Leone, from October 2015 to January 2016. A blood sample was collected from 187 study participants, 132 negative controls (individuals with a low likelihood of previous exposure to Ebola virus), and 30 positive controls (Ebola virus disease survivors). IgG responses to Ebola glycoprotein and nucleoprotein were measured using Alpha Diagnostic International ELISA kits with plasma diluted at 1:200. Optical density was read at 450 nm (subtracting OD at 630nm to normalize well background) on a ChroMate 4300 microplate reader. A cutoff of 4.7 U/mL for the anti-GP ELISA yielded 96.7% sensitivity and 97.7% specificity in distinguishing positive and negative controls. We identified 14 seropositive individuals not known to have had Ebola virus disease. Two of the 14 seropositive individuals reported only fever during quarantine while the remaining 12 denied any signs or symptoms during quarantine. CONCLUSIONS/SIGNIFICANCE: By using ELISA to measure Zaire Ebola virus antibody concentrations, we identified a significant number of individuals with previously undetected EBOV infection in a ‘hotspot’ village in Sierra Leone, approximately one year after the village outbreak. The findings provide further evidence that Ebola, like many other viral infections, presents with a spectrum of clinical manifestations, including minimally symptomatic infection. These data also suggest that a significant portion of Ebola transmission events may have gone undetected during the outbreak. Further studies are needed to understand the potential risk of transmission and clinical sequelae in individuals with previously undetected EBOV infection. Public Library of Science 2016-11-15 /pmc/articles/PMC5112953/ /pubmed/27846221 http://dx.doi.org/10.1371/journal.pntd.0005087 Text en © 2016 Richardson 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 Richardson, Eugene T. Kelly, J. Daniel Barrie, Mohamed Bailor Mesman, Annelies W. Karku, Sahr Quiwa, Komba Marsh, Regan H. Koedoyoma, Songor Daboh, Fodei Barron, Kathryn P. Grady, Michael Tucker, Elizabeth Dierberg, Kerry L. Rutherford, George W. Barry, Michele Jones, James Holland Murray, Megan B. Farmer, Paul E. Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title | Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title_full | Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title_fullStr | Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title_full_unstemmed | Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title_short | Minimally Symptomatic Infection in an Ebola ‘Hotspot’: A Cross-Sectional Serosurvey |
title_sort | minimally symptomatic infection in an ebola ‘hotspot’: a cross-sectional serosurvey |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112953/ https://www.ncbi.nlm.nih.gov/pubmed/27846221 http://dx.doi.org/10.1371/journal.pntd.0005087 |
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