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Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant

Recent phylodynamic studies have focused on using tree topology patterns to elucidate interactions among the epidemiological, evolutionary, and demographic characteristics of infectious agents. However, because studies of viral phylodynamics tend to focus on epidemic outbreaks, tree topology signatu...

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Autores principales: Yen, Yung-Chang, Chu, Pei-Huan, Lu, Po-Liang, Lin, Yung-Cheng, Shi, Yong-Ying, Chou, Li-Chiu, Wang, Chu-Feng, Lin, Yi-Ying, Su, Hui-Ju, Lin, Chien-Ching, Zeng, Jing-Yun, Tyan, Yu-Chang, Ke, Guan-Ming, Chu, Pei-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987047/
https://www.ncbi.nlm.nih.gov/pubmed/27529556
http://dx.doi.org/10.1371/journal.pone.0160672
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author Yen, Yung-Chang
Chu, Pei-Huan
Lu, Po-Liang
Lin, Yung-Cheng
Shi, Yong-Ying
Chou, Li-Chiu
Wang, Chu-Feng
Lin, Yi-Ying
Su, Hui-Ju
Lin, Chien-Ching
Zeng, Jing-Yun
Tyan, Yu-Chang
Ke, Guan-Ming
Chu, Pei-Yu
author_facet Yen, Yung-Chang
Chu, Pei-Huan
Lu, Po-Liang
Lin, Yung-Cheng
Shi, Yong-Ying
Chou, Li-Chiu
Wang, Chu-Feng
Lin, Yi-Ying
Su, Hui-Ju
Lin, Chien-Ching
Zeng, Jing-Yun
Tyan, Yu-Chang
Ke, Guan-Ming
Chu, Pei-Yu
author_sort Yen, Yung-Chang
collection PubMed
description Recent phylodynamic studies have focused on using tree topology patterns to elucidate interactions among the epidemiological, evolutionary, and demographic characteristics of infectious agents. However, because studies of viral phylodynamics tend to focus on epidemic outbreaks, tree topology signatures of tissue-tropism pathogens might not be clearly identified. Therefore, this study used a novel Bayesian evolutionary approach to analyze the A24 variant of coxsackievirus (CV-A24v), an ocular-tropism agent of acute hemorrhagic conjunctivitis. Analyses of the 915-nucleotide VP1 and 690-nt 3D(pol) regions of 21 strains isolated in Taiwan and worldwide during 1985–2010 revealed a clear chronological trend in both the VP1 and 3D(pol) phylogenetic trees: the emergence of a single dominant cluster in each outbreak. The VP1 sequences included three genotypes: GI (prototype), GIII (isolated 1985–1999), and GIV (isolated after 2000); no VP1 sequences from GII strains have been deposited in GenBank. Another five genotypes identified in the 3D(pol) region had support values >0.9. Geographic and demographic transitions among CV-A24v clusters were clearly identified by Bayes algorithm. The transmission route was mapped from India to China and then to Taiwan, and each prevalent viral population declined before new clusters emerged. Notably, the VP1 and 3D(pol) genes had high nucleotide sequence similarities (94.1% and 95.2%, respectively). The lack of co-circulating lineages and narrow tissue tropism affected the CV-A24v gene pool.
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spelling pubmed-49870472016-08-29 Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant Yen, Yung-Chang Chu, Pei-Huan Lu, Po-Liang Lin, Yung-Cheng Shi, Yong-Ying Chou, Li-Chiu Wang, Chu-Feng Lin, Yi-Ying Su, Hui-Ju Lin, Chien-Ching Zeng, Jing-Yun Tyan, Yu-Chang Ke, Guan-Ming Chu, Pei-Yu PLoS One Research Article Recent phylodynamic studies have focused on using tree topology patterns to elucidate interactions among the epidemiological, evolutionary, and demographic characteristics of infectious agents. However, because studies of viral phylodynamics tend to focus on epidemic outbreaks, tree topology signatures of tissue-tropism pathogens might not be clearly identified. Therefore, this study used a novel Bayesian evolutionary approach to analyze the A24 variant of coxsackievirus (CV-A24v), an ocular-tropism agent of acute hemorrhagic conjunctivitis. Analyses of the 915-nucleotide VP1 and 690-nt 3D(pol) regions of 21 strains isolated in Taiwan and worldwide during 1985–2010 revealed a clear chronological trend in both the VP1 and 3D(pol) phylogenetic trees: the emergence of a single dominant cluster in each outbreak. The VP1 sequences included three genotypes: GI (prototype), GIII (isolated 1985–1999), and GIV (isolated after 2000); no VP1 sequences from GII strains have been deposited in GenBank. Another five genotypes identified in the 3D(pol) region had support values >0.9. Geographic and demographic transitions among CV-A24v clusters were clearly identified by Bayes algorithm. The transmission route was mapped from India to China and then to Taiwan, and each prevalent viral population declined before new clusters emerged. Notably, the VP1 and 3D(pol) genes had high nucleotide sequence similarities (94.1% and 95.2%, respectively). The lack of co-circulating lineages and narrow tissue tropism affected the CV-A24v gene pool. Public Library of Science 2016-08-16 /pmc/articles/PMC4987047/ /pubmed/27529556 http://dx.doi.org/10.1371/journal.pone.0160672 Text en © 2016 Yen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yen, Yung-Chang
Chu, Pei-Huan
Lu, Po-Liang
Lin, Yung-Cheng
Shi, Yong-Ying
Chou, Li-Chiu
Wang, Chu-Feng
Lin, Yi-Ying
Su, Hui-Ju
Lin, Chien-Ching
Zeng, Jing-Yun
Tyan, Yu-Chang
Ke, Guan-Ming
Chu, Pei-Yu
Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title_full Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title_fullStr Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title_full_unstemmed Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title_short Phylodynamic Characterization of an Ocular-Tropism Coxsackievirus A24 Variant
title_sort phylodynamic characterization of an ocular-tropism coxsackievirus a24 variant
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987047/
https://www.ncbi.nlm.nih.gov/pubmed/27529556
http://dx.doi.org/10.1371/journal.pone.0160672
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