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High prevalence of hepatitis delta virus in Cameroon
Hepatitis delta virus (HDV), a satellite virus of hepatitis B virus (HBV), infects an estimated 15–20 million people worldwide and confers a greater risk for accelerated progression to liver disease. However, limited HDV surveillance data are available in sub-Saharan Africa where HDV diversity is hi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072717/ https://www.ncbi.nlm.nih.gov/pubmed/30072752 http://dx.doi.org/10.1038/s41598-018-30078-5 |
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author | Butler, Emily K. Rodgers, Mary A. Coller, Kelly E. Barnaby, Devin Krilich, Elizabeth Olivo, Ana Cassidy, Michael Mbanya, Dora Kaptue, Lazare Ndembi, Nicaise Cloherty, Gavin |
author_facet | Butler, Emily K. Rodgers, Mary A. Coller, Kelly E. Barnaby, Devin Krilich, Elizabeth Olivo, Ana Cassidy, Michael Mbanya, Dora Kaptue, Lazare Ndembi, Nicaise Cloherty, Gavin |
author_sort | Butler, Emily K. |
collection | PubMed |
description | Hepatitis delta virus (HDV), a satellite virus of hepatitis B virus (HBV), infects an estimated 15–20 million people worldwide and confers a greater risk for accelerated progression to liver disease. However, limited HDV surveillance data are available in sub-Saharan Africa where HDV diversity is high. To determine the prevalence and diversity of HDV in Cameroon, serological and molecular characterization was performed on 1928 HBsAg positive specimens selected from retrospective viral surveillance studies conducted in Cameroon from 2010–2016. Samples were screened for HDV antibodies on the Abbott ARCHITECT instrument and for HDV RNA on the Abbott m2000 instrument by research assays. HDV positive specimens with sufficient viral load were selected for genomic sequencing. The seroprevalence of HDV in HBsAg positive samples from Cameroon was 46.73% [95% CI; 44.51–48.96%], with prevalence of active HDV infection being 34.2% [95% CI; 32.09–36.41%]. HDV genotypes 1, 6, 7 and 8 were identified amongst N = 211 sequences, including N = 145 genomes. HDV prevalence is high within the study cohort, indicating that a large portion of HBV infected individuals in Cameroon are at elevated risk for severe hepatitis and death. Collectively, these results emphasize the need for HBV vaccination and HDV testing in HBsAg positive patients in Cameroon. |
format | Online Article Text |
id | pubmed-6072717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60727172018-08-06 High prevalence of hepatitis delta virus in Cameroon Butler, Emily K. Rodgers, Mary A. Coller, Kelly E. Barnaby, Devin Krilich, Elizabeth Olivo, Ana Cassidy, Michael Mbanya, Dora Kaptue, Lazare Ndembi, Nicaise Cloherty, Gavin Sci Rep Article Hepatitis delta virus (HDV), a satellite virus of hepatitis B virus (HBV), infects an estimated 15–20 million people worldwide and confers a greater risk for accelerated progression to liver disease. However, limited HDV surveillance data are available in sub-Saharan Africa where HDV diversity is high. To determine the prevalence and diversity of HDV in Cameroon, serological and molecular characterization was performed on 1928 HBsAg positive specimens selected from retrospective viral surveillance studies conducted in Cameroon from 2010–2016. Samples were screened for HDV antibodies on the Abbott ARCHITECT instrument and for HDV RNA on the Abbott m2000 instrument by research assays. HDV positive specimens with sufficient viral load were selected for genomic sequencing. The seroprevalence of HDV in HBsAg positive samples from Cameroon was 46.73% [95% CI; 44.51–48.96%], with prevalence of active HDV infection being 34.2% [95% CI; 32.09–36.41%]. HDV genotypes 1, 6, 7 and 8 were identified amongst N = 211 sequences, including N = 145 genomes. HDV prevalence is high within the study cohort, indicating that a large portion of HBV infected individuals in Cameroon are at elevated risk for severe hepatitis and death. Collectively, these results emphasize the need for HBV vaccination and HDV testing in HBsAg positive patients in Cameroon. Nature Publishing Group UK 2018-08-02 /pmc/articles/PMC6072717/ /pubmed/30072752 http://dx.doi.org/10.1038/s41598-018-30078-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Butler, Emily K. Rodgers, Mary A. Coller, Kelly E. Barnaby, Devin Krilich, Elizabeth Olivo, Ana Cassidy, Michael Mbanya, Dora Kaptue, Lazare Ndembi, Nicaise Cloherty, Gavin High prevalence of hepatitis delta virus in Cameroon |
title | High prevalence of hepatitis delta virus in Cameroon |
title_full | High prevalence of hepatitis delta virus in Cameroon |
title_fullStr | High prevalence of hepatitis delta virus in Cameroon |
title_full_unstemmed | High prevalence of hepatitis delta virus in Cameroon |
title_short | High prevalence of hepatitis delta virus in Cameroon |
title_sort | high prevalence of hepatitis delta virus in cameroon |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072717/ https://www.ncbi.nlm.nih.gov/pubmed/30072752 http://dx.doi.org/10.1038/s41598-018-30078-5 |
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