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Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009
Coxsackievirus A24 variant (CVA24v) is a major causative agent of acute hemorrhagic conjunctivitis outbreaks worldwide, yet the evolutionary and transmission dynamics of the virus remain unclear. To address this, we analyzed and compared the 3C and partial VP1 gene regions of CVA24v isolates obtaine...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427094/ https://www.ncbi.nlm.nih.gov/pubmed/32792520 http://dx.doi.org/10.1038/s41598-020-70436-w |
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author | Fonseca, Magilé C. Pupo-Meriño, Mario García-González, Luis A. Resik, Sonia Hung, Lai Heng Muné, Mayra Rodríguez, Hermis Morier, Luis Norder, Heléne Sarmiento, Luis |
author_facet | Fonseca, Magilé C. Pupo-Meriño, Mario García-González, Luis A. Resik, Sonia Hung, Lai Heng Muné, Mayra Rodríguez, Hermis Morier, Luis Norder, Heléne Sarmiento, Luis |
author_sort | Fonseca, Magilé C. |
collection | PubMed |
description | Coxsackievirus A24 variant (CVA24v) is a major causative agent of acute hemorrhagic conjunctivitis outbreaks worldwide, yet the evolutionary and transmission dynamics of the virus remain unclear. To address this, we analyzed and compared the 3C and partial VP1 gene regions of CVA24v isolates obtained from five outbreaks in Cuba between 1986 and 2009 and strains isolated worldwide. Here we show that Cuban strains were homologous to those isolated in Africa, the Americas and Asia during the same time period. Two genotypes of CVA24v (GIII and GIV) were repeatedly introduced into Cuba and they arose about two years before the epidemic was detected. The two genotypes co-evolved with a population size that is stable over time. However, nucleotide substitution rates peaked during pandemics with 4.39 × 10(−3) and 5.80 × 10(−3) substitutions per site per year for the 3C and VP1 region, respectively. The phylogeographic analysis identified 25 and 19 viral transmission routes based on 3C and VP1 regions, respectively. Pandemic viruses usually originated in Asia, and both China and Brazil were the major hub for the global dispersal of the virus. Together, these data provide novel insight into the epidemiological dynamics of this virus and possibly other pandemic viruses. |
format | Online Article Text |
id | pubmed-7427094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74270942020-08-18 Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 Fonseca, Magilé C. Pupo-Meriño, Mario García-González, Luis A. Resik, Sonia Hung, Lai Heng Muné, Mayra Rodríguez, Hermis Morier, Luis Norder, Heléne Sarmiento, Luis Sci Rep Article Coxsackievirus A24 variant (CVA24v) is a major causative agent of acute hemorrhagic conjunctivitis outbreaks worldwide, yet the evolutionary and transmission dynamics of the virus remain unclear. To address this, we analyzed and compared the 3C and partial VP1 gene regions of CVA24v isolates obtained from five outbreaks in Cuba between 1986 and 2009 and strains isolated worldwide. Here we show that Cuban strains were homologous to those isolated in Africa, the Americas and Asia during the same time period. Two genotypes of CVA24v (GIII and GIV) were repeatedly introduced into Cuba and they arose about two years before the epidemic was detected. The two genotypes co-evolved with a population size that is stable over time. However, nucleotide substitution rates peaked during pandemics with 4.39 × 10(−3) and 5.80 × 10(−3) substitutions per site per year for the 3C and VP1 region, respectively. The phylogeographic analysis identified 25 and 19 viral transmission routes based on 3C and VP1 regions, respectively. Pandemic viruses usually originated in Asia, and both China and Brazil were the major hub for the global dispersal of the virus. Together, these data provide novel insight into the epidemiological dynamics of this virus and possibly other pandemic viruses. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7427094/ /pubmed/32792520 http://dx.doi.org/10.1038/s41598-020-70436-w Text en © The Author(s) 2020 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 Fonseca, Magilé C. Pupo-Meriño, Mario García-González, Luis A. Resik, Sonia Hung, Lai Heng Muné, Mayra Rodríguez, Hermis Morier, Luis Norder, Heléne Sarmiento, Luis Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title | Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title_full | Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title_fullStr | Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title_full_unstemmed | Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title_short | Molecular evolution of coxsackievirus A24v in Cuba over 23-years, 1986–2009 |
title_sort | molecular evolution of coxsackievirus a24v in cuba over 23-years, 1986–2009 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7427094/ https://www.ncbi.nlm.nih.gov/pubmed/32792520 http://dx.doi.org/10.1038/s41598-020-70436-w |
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