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Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China

Human mastadenovirus species C (HAdV-C) are the most common etiologic agents of respiratory disease in young children and are frequently detected worldwide including China. Two recombinant HAdV-C strains (BJ04 and BJ09) were isolated from infants with acute respiratory infection (ARI) in Beijing in...

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Autores principales: Mao, Naiying, Zhu, Zhen, Rivailler, Pierre, Chen, Meng, Fan, Qin, Huang, Fang, Xu, Wenbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684218/
https://www.ncbi.nlm.nih.gov/pubmed/29133946
http://dx.doi.org/10.1038/s41598-017-15336-2
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author Mao, Naiying
Zhu, Zhen
Rivailler, Pierre
Chen, Meng
Fan, Qin
Huang, Fang
Xu, Wenbo
author_facet Mao, Naiying
Zhu, Zhen
Rivailler, Pierre
Chen, Meng
Fan, Qin
Huang, Fang
Xu, Wenbo
author_sort Mao, Naiying
collection PubMed
description Human mastadenovirus species C (HAdV-C) are the most common etiologic agents of respiratory disease in young children and are frequently detected worldwide including China. Two recombinant HAdV-C strains (BJ04 and BJ09) were isolated from infants with acute respiratory infection (ARI) in Beijing in 2012–2013. The whole genome sequences (WGS) of BJ04 and BJ09 were generated and compared to other 35 HAdV-C WGSs publicly available. Phylogenetic analyses showed that the BJ04 strain might be the result of three homologous recombination events involving the parental strains JX173086 (HAdV-1), NC_001405 (HAdV-2) and LC068718 (HAdV-6), whereas BJ09 viral genome might be made of genetic elements from JX173083 (HAdV-1), KF268199 (HAdV-5), and KR699642 (strain CBJ113). Despite intratypic recombination, amino acid analysis showed that the gene repertoire of BJ04 and BJ09 were similar to type 2 viruses. Finally, this analysis revealed that at least three lineages of HAdV-C have been identified in China, represented by BJ04 related to NC_001405, BJ09 related to CBJ113, and KF951595 (strain DD28) related to virus isolated in Japan. This study showed that the frequent recombination played an important driving force for complexity of the HAdV-C epidemic in Beijing, thereby demonstrating the necessity for epidemiological and virological surveillance for HAdV-C in China.
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spelling pubmed-56842182017-11-21 Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China Mao, Naiying Zhu, Zhen Rivailler, Pierre Chen, Meng Fan, Qin Huang, Fang Xu, Wenbo Sci Rep Article Human mastadenovirus species C (HAdV-C) are the most common etiologic agents of respiratory disease in young children and are frequently detected worldwide including China. Two recombinant HAdV-C strains (BJ04 and BJ09) were isolated from infants with acute respiratory infection (ARI) in Beijing in 2012–2013. The whole genome sequences (WGS) of BJ04 and BJ09 were generated and compared to other 35 HAdV-C WGSs publicly available. Phylogenetic analyses showed that the BJ04 strain might be the result of three homologous recombination events involving the parental strains JX173086 (HAdV-1), NC_001405 (HAdV-2) and LC068718 (HAdV-6), whereas BJ09 viral genome might be made of genetic elements from JX173083 (HAdV-1), KF268199 (HAdV-5), and KR699642 (strain CBJ113). Despite intratypic recombination, amino acid analysis showed that the gene repertoire of BJ04 and BJ09 were similar to type 2 viruses. Finally, this analysis revealed that at least three lineages of HAdV-C have been identified in China, represented by BJ04 related to NC_001405, BJ09 related to CBJ113, and KF951595 (strain DD28) related to virus isolated in Japan. This study showed that the frequent recombination played an important driving force for complexity of the HAdV-C epidemic in Beijing, thereby demonstrating the necessity for epidemiological and virological surveillance for HAdV-C in China. Nature Publishing Group UK 2017-11-13 /pmc/articles/PMC5684218/ /pubmed/29133946 http://dx.doi.org/10.1038/s41598-017-15336-2 Text en © The Author(s) 2017 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
Mao, Naiying
Zhu, Zhen
Rivailler, Pierre
Chen, Meng
Fan, Qin
Huang, Fang
Xu, Wenbo
Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title_full Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title_fullStr Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title_full_unstemmed Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title_short Whole genomic analysis of two potential recombinant strains within Human mastadenovirus species C previously found in Beijing, China
title_sort whole genomic analysis of two potential recombinant strains within human mastadenovirus species c previously found in beijing, china
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684218/
https://www.ncbi.nlm.nih.gov/pubmed/29133946
http://dx.doi.org/10.1038/s41598-017-15336-2
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