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Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs
Co-infections with human immunodeficiency virus type 1 (HIV-1) and human pegivirus (HPgV) are common in hepatitis C virus (HCV)-infected individuals. However, analysis on the evolutionary dynamics and transmission network profiles of these viruses among individuals with multiple infections remains l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602306/ https://www.ncbi.nlm.nih.gov/pubmed/26459957 http://dx.doi.org/10.1038/srep15198 |
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author | Tien Ng, Kim Takebe, Yutaka Bee Chook, Jack Zhen Chow, Wei Gan Chan, Kok Abed Al-Darraji, Haider Abdulrazzaq Kamarulzaman, Adeeba Keng Tee, Kok |
author_facet | Tien Ng, Kim Takebe, Yutaka Bee Chook, Jack Zhen Chow, Wei Gan Chan, Kok Abed Al-Darraji, Haider Abdulrazzaq Kamarulzaman, Adeeba Keng Tee, Kok |
author_sort | Tien Ng, Kim |
collection | PubMed |
description | Co-infections with human immunodeficiency virus type 1 (HIV-1) and human pegivirus (HPgV) are common in hepatitis C virus (HCV)-infected individuals. However, analysis on the evolutionary dynamics and transmission network profiles of these viruses among individuals with multiple infections remains limited. A total of 228 injecting drug users (IDUs), either HCV- and/or HIV-1-infected, were recruited in Kuala Lumpur, Malaysia. HCV, HIV-1 and HPgV genes were sequenced, with epidemic growth rates assessed by the Bayesian coalescent method. Based on the sequence data, mono-, dual- and triple-infection were detected in 38.8%, 40.6% and 20.6% of the subjects, respectively. Fifteen transmission networks involving HCV (subtype 1a, 1b, 3a and 3b), HIV-1 (CRF33_01B) and HPgV (genotype 2) were identified and characterized. Genealogical estimates indicated that the predominant HCV, HIV-1 and HPgV genotypes were introduced into the IDUs population through multiple sub-epidemics that emerged as early as 1950s (HCV), 1980s (HIV-1) and 1990s (HPgV). By determining the difference in divergence times between viral lineages (ΔtMRCA), we also showed that the frequency of viral co-transmission is low among these IDUs. Despite increased access to therapy and other harm reduction interventions, the continuous emergence and coexistence of new transmission networks suggest persistent multiple viral transmissions among IDUs. |
format | Online Article Text |
id | pubmed-4602306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46023062015-10-23 Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs Tien Ng, Kim Takebe, Yutaka Bee Chook, Jack Zhen Chow, Wei Gan Chan, Kok Abed Al-Darraji, Haider Abdulrazzaq Kamarulzaman, Adeeba Keng Tee, Kok Sci Rep Article Co-infections with human immunodeficiency virus type 1 (HIV-1) and human pegivirus (HPgV) are common in hepatitis C virus (HCV)-infected individuals. However, analysis on the evolutionary dynamics and transmission network profiles of these viruses among individuals with multiple infections remains limited. A total of 228 injecting drug users (IDUs), either HCV- and/or HIV-1-infected, were recruited in Kuala Lumpur, Malaysia. HCV, HIV-1 and HPgV genes were sequenced, with epidemic growth rates assessed by the Bayesian coalescent method. Based on the sequence data, mono-, dual- and triple-infection were detected in 38.8%, 40.6% and 20.6% of the subjects, respectively. Fifteen transmission networks involving HCV (subtype 1a, 1b, 3a and 3b), HIV-1 (CRF33_01B) and HPgV (genotype 2) were identified and characterized. Genealogical estimates indicated that the predominant HCV, HIV-1 and HPgV genotypes were introduced into the IDUs population through multiple sub-epidemics that emerged as early as 1950s (HCV), 1980s (HIV-1) and 1990s (HPgV). By determining the difference in divergence times between viral lineages (ΔtMRCA), we also showed that the frequency of viral co-transmission is low among these IDUs. Despite increased access to therapy and other harm reduction interventions, the continuous emergence and coexistence of new transmission networks suggest persistent multiple viral transmissions among IDUs. Nature Publishing Group 2015-10-13 /pmc/articles/PMC4602306/ /pubmed/26459957 http://dx.doi.org/10.1038/srep15198 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tien Ng, Kim Takebe, Yutaka Bee Chook, Jack Zhen Chow, Wei Gan Chan, Kok Abed Al-Darraji, Haider Abdulrazzaq Kamarulzaman, Adeeba Keng Tee, Kok Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title | Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title_full | Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title_fullStr | Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title_full_unstemmed | Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title_short | Co-infections and transmission networks of HCV, HIV-1 and HPgV among people who inject drugs |
title_sort | co-infections and transmission networks of hcv, hiv-1 and hpgv among people who inject drugs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602306/ https://www.ncbi.nlm.nih.gov/pubmed/26459957 http://dx.doi.org/10.1038/srep15198 |
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