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Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo
OBJECTIVES: With limited data available from Central Africa, the aim of our study was to evaluate the anti-SARS-CoV-2 Ab prevalence in indigenous residents of Bomassa, a village located in the Sangha region in the Republic of Congo. METHODS: Plasma and oropharyngeal swab samples were collected from...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760703/ https://www.ncbi.nlm.nih.gov/pubmed/35721438 http://dx.doi.org/10.1016/j.ijregi.2022.01.002 |
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author | Lobaloba Ingoba, Line Djontu, Jean Claude Mfoutou Mapanguy, Claujens Chastel Mouzinga, Freisnel Diafouka Kietela, Steve Vouvoungui, Christevy Kuisma, Eeva Nguimbi, Etienne Ntoumi, Francine |
author_facet | Lobaloba Ingoba, Line Djontu, Jean Claude Mfoutou Mapanguy, Claujens Chastel Mouzinga, Freisnel Diafouka Kietela, Steve Vouvoungui, Christevy Kuisma, Eeva Nguimbi, Etienne Ntoumi, Francine |
author_sort | Lobaloba Ingoba, Line |
collection | PubMed |
description | OBJECTIVES: With limited data available from Central Africa, the aim of our study was to evaluate the anti-SARS-CoV-2 Ab prevalence in indigenous residents of Bomassa, a village located in the Sangha region in the Republic of Congo. METHODS: Plasma and oropharyngeal swab samples were collected from 304 healthy adult individuals, randomly recruited in May 2021 before vaccine introduction in the area. In addition, 82 plasma samples from the same area in 2019 were included as controls for the investigation of cross-reactivity against other coronaviruses. The SARS-CoV-2 virus was detected by qRT-PCR and sequenced using next-generation sequencing. ELISA was used for detecting IgG, IgM, and neutralizing Ab against SARS-CoV-2 antigens. RESULTS: Around 4.9% (15/304) of the participants were SARS-CoV-2 positive, with B.1.631 being the only variant identified. Of 109 individuals harboring anti-SARS-CoV-2 IgG and/or IgM Ab, 45.9% (50/109) had anti-SARS-CoV-2 neutralizing Ab. Of the control samples collected before the pandemic, 3.7% (3/82) were positive for IgG, but negative for neutralizing Ab. CONCLUSIONS: Seroprevalence against SARS-CoV-2 occurred in 25% of the indigenous population sample, with almost 50% of these seropositive participants possessing neutralizing antibodies. These findings suggest that the spread of SARS-CoV-2 has been underestimated in the Republic of Congo. |
format | Online Article Text |
id | pubmed-8760703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87607032022-01-18 Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo Lobaloba Ingoba, Line Djontu, Jean Claude Mfoutou Mapanguy, Claujens Chastel Mouzinga, Freisnel Diafouka Kietela, Steve Vouvoungui, Christevy Kuisma, Eeva Nguimbi, Etienne Ntoumi, Francine IJID Reg Coronavirus (COVID-19) Collection OBJECTIVES: With limited data available from Central Africa, the aim of our study was to evaluate the anti-SARS-CoV-2 Ab prevalence in indigenous residents of Bomassa, a village located in the Sangha region in the Republic of Congo. METHODS: Plasma and oropharyngeal swab samples were collected from 304 healthy adult individuals, randomly recruited in May 2021 before vaccine introduction in the area. In addition, 82 plasma samples from the same area in 2019 were included as controls for the investigation of cross-reactivity against other coronaviruses. The SARS-CoV-2 virus was detected by qRT-PCR and sequenced using next-generation sequencing. ELISA was used for detecting IgG, IgM, and neutralizing Ab against SARS-CoV-2 antigens. RESULTS: Around 4.9% (15/304) of the participants were SARS-CoV-2 positive, with B.1.631 being the only variant identified. Of 109 individuals harboring anti-SARS-CoV-2 IgG and/or IgM Ab, 45.9% (50/109) had anti-SARS-CoV-2 neutralizing Ab. Of the control samples collected before the pandemic, 3.7% (3/82) were positive for IgG, but negative for neutralizing Ab. CONCLUSIONS: Seroprevalence against SARS-CoV-2 occurred in 25% of the indigenous population sample, with almost 50% of these seropositive participants possessing neutralizing antibodies. These findings suggest that the spread of SARS-CoV-2 has been underestimated in the Republic of Congo. Elsevier 2022-01-15 /pmc/articles/PMC8760703/ /pubmed/35721438 http://dx.doi.org/10.1016/j.ijregi.2022.01.002 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Coronavirus (COVID-19) Collection Lobaloba Ingoba, Line Djontu, Jean Claude Mfoutou Mapanguy, Claujens Chastel Mouzinga, Freisnel Diafouka Kietela, Steve Vouvoungui, Christevy Kuisma, Eeva Nguimbi, Etienne Ntoumi, Francine Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title | Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title_full | Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title_fullStr | Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title_full_unstemmed | Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title_short | Seroprevalence of anti-SARS-CoV-2 antibodies in a population living in Bomassa village, Republic of Congo |
title_sort | seroprevalence of anti-sars-cov-2 antibodies in a population living in bomassa village, republic of congo |
topic | Coronavirus (COVID-19) Collection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760703/ https://www.ncbi.nlm.nih.gov/pubmed/35721438 http://dx.doi.org/10.1016/j.ijregi.2022.01.002 |
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