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Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017

In Cambodia, little epidemiological data of hepatitis C virus (HCV) is available. All previous studies were limited to only small or specific populations. In the present study, we performed a characterization of HCV genetic diversity based on demography, clinical data, and phylogenetic analysis of H...

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Autores principales: Nouhin, Janin, Iwamoto, Momoko, Prak, Sophearot, Dousset, Jean-Philippe, Phon, Kerya, Heng, Seiha, Kerleguer, Alexandra, Le Paih, Mickaël, Dussart, Philippe, Maman, David, Rouet, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514207/
https://www.ncbi.nlm.nih.gov/pubmed/31086236
http://dx.doi.org/10.1038/s41598-019-43785-4
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author Nouhin, Janin
Iwamoto, Momoko
Prak, Sophearot
Dousset, Jean-Philippe
Phon, Kerya
Heng, Seiha
Kerleguer, Alexandra
Le Paih, Mickaël
Dussart, Philippe
Maman, David
Rouet, François
author_facet Nouhin, Janin
Iwamoto, Momoko
Prak, Sophearot
Dousset, Jean-Philippe
Phon, Kerya
Heng, Seiha
Kerleguer, Alexandra
Le Paih, Mickaël
Dussart, Philippe
Maman, David
Rouet, François
author_sort Nouhin, Janin
collection PubMed
description In Cambodia, little epidemiological data of hepatitis C virus (HCV) is available. All previous studies were limited to only small or specific populations. In the present study, we performed a characterization of HCV genetic diversity based on demography, clinical data, and phylogenetic analysis of HCV non-structural 5B (NS5B) sequences belonging to a large cohort of patients (n = 3,133) coming from majority part of Cambodia between September 2016 and December 2017. The phylogenetic analysis revealed that HCV genotype 1 and 6 were the most predominant and sharing equal proportions (46%). The remaining genotypes were genotype 2 (4.3%) and unclassified variants (3.6%). Among genotype 1, subtype 1b was the most prevalent subtype accounting for 94%. Within genotype 6, we observed a high degree of diversity and the most common viral subtypes were 6e (44%) and 6r (23%). This characteristic points to the longstanding history of HCV in Cambodia. Geographic specificity of viral genotype was not observed. Risks of HCV infection were mainly associated with experience of an invasive medical procedure (64.7%), having partner with HCV (19.5%), and blood transfusion (9.9%). In addition, all of these factors were comparable among different HCV genotypes. All these features define the specificity of HCV epidemiology in Cambodia.
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spelling pubmed-65142072019-05-24 Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017 Nouhin, Janin Iwamoto, Momoko Prak, Sophearot Dousset, Jean-Philippe Phon, Kerya Heng, Seiha Kerleguer, Alexandra Le Paih, Mickaël Dussart, Philippe Maman, David Rouet, François Sci Rep Article In Cambodia, little epidemiological data of hepatitis C virus (HCV) is available. All previous studies were limited to only small or specific populations. In the present study, we performed a characterization of HCV genetic diversity based on demography, clinical data, and phylogenetic analysis of HCV non-structural 5B (NS5B) sequences belonging to a large cohort of patients (n = 3,133) coming from majority part of Cambodia between September 2016 and December 2017. The phylogenetic analysis revealed that HCV genotype 1 and 6 were the most predominant and sharing equal proportions (46%). The remaining genotypes were genotype 2 (4.3%) and unclassified variants (3.6%). Among genotype 1, subtype 1b was the most prevalent subtype accounting for 94%. Within genotype 6, we observed a high degree of diversity and the most common viral subtypes were 6e (44%) and 6r (23%). This characteristic points to the longstanding history of HCV in Cambodia. Geographic specificity of viral genotype was not observed. Risks of HCV infection were mainly associated with experience of an invasive medical procedure (64.7%), having partner with HCV (19.5%), and blood transfusion (9.9%). In addition, all of these factors were comparable among different HCV genotypes. All these features define the specificity of HCV epidemiology in Cambodia. Nature Publishing Group UK 2019-05-13 /pmc/articles/PMC6514207/ /pubmed/31086236 http://dx.doi.org/10.1038/s41598-019-43785-4 Text en © The Author(s) 2019 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
Nouhin, Janin
Iwamoto, Momoko
Prak, Sophearot
Dousset, Jean-Philippe
Phon, Kerya
Heng, Seiha
Kerleguer, Alexandra
Le Paih, Mickaël
Dussart, Philippe
Maman, David
Rouet, François
Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title_full Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title_fullStr Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title_full_unstemmed Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title_short Molecular epidemiology of hepatitis C virus in Cambodia during 2016–2017
title_sort molecular epidemiology of hepatitis c virus in cambodia during 2016–2017
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514207/
https://www.ncbi.nlm.nih.gov/pubmed/31086236
http://dx.doi.org/10.1038/s41598-019-43785-4
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