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Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai
Human adenovirus F (HAdV-F) is one of the major causative species detected in acute gastroenteritis in children worldwide. HAdV-F is composed of serotypes 40 and 41. Most studies have reported the prevalence of HAdV-41 and focused on its epidemiologic characteristics. In this study, seventeen sample...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471248/ https://www.ncbi.nlm.nih.gov/pubmed/28615624 http://dx.doi.org/10.1038/s41598-017-01293-3 |
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author | Li, Peng Yang, Lang Guo, Jiayin Zou, Wenwei Xu, Xuebin Yang, Xiaoxia Du, Xinying Qiu, Shaofu Song, Hongbin |
author_facet | Li, Peng Yang, Lang Guo, Jiayin Zou, Wenwei Xu, Xuebin Yang, Xiaoxia Du, Xinying Qiu, Shaofu Song, Hongbin |
author_sort | Li, Peng |
collection | PubMed |
description | Human adenovirus F (HAdV-F) is one of the major causative species detected in acute gastroenteritis in children worldwide. HAdV-F is composed of serotypes 40 and 41. Most studies have reported the prevalence of HAdV-41 and focused on its epidemiologic characteristics. In this study, seventeen samples were identified as HAdV-41 out of 273 fecal specimens from children with acute diarrhea in Shanghai. Five isolates were isolated and subjected to whole genome sequencing and analysis to characterize the genetic variation and evolution. Full genome analysis revealed low genetic variation (99.07–99.92% identity) among the isolates, and InDels are observed in the E2A gene and the hexon gene compared to the reference strain NIVD103. Phylogenetic analysis showed that all isolates mainly formed two genome-type clusters but with incongruence in the trees of whole genomes and individual genes. The recombination breakpoints of the five isolates were inferred by the Recombination Detection Program (RDP) and varied in the number and location of the recombination events, indicating different evolution origins. Overall, our study highlights the genetic diversity of HAdV-41 isolates circulating in Shanghai, which may have evolved from inter-strain recombination. |
format | Online Article Text |
id | pubmed-5471248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54712482017-06-19 Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai Li, Peng Yang, Lang Guo, Jiayin Zou, Wenwei Xu, Xuebin Yang, Xiaoxia Du, Xinying Qiu, Shaofu Song, Hongbin Sci Rep Article Human adenovirus F (HAdV-F) is one of the major causative species detected in acute gastroenteritis in children worldwide. HAdV-F is composed of serotypes 40 and 41. Most studies have reported the prevalence of HAdV-41 and focused on its epidemiologic characteristics. In this study, seventeen samples were identified as HAdV-41 out of 273 fecal specimens from children with acute diarrhea in Shanghai. Five isolates were isolated and subjected to whole genome sequencing and analysis to characterize the genetic variation and evolution. Full genome analysis revealed low genetic variation (99.07–99.92% identity) among the isolates, and InDels are observed in the E2A gene and the hexon gene compared to the reference strain NIVD103. Phylogenetic analysis showed that all isolates mainly formed two genome-type clusters but with incongruence in the trees of whole genomes and individual genes. The recombination breakpoints of the five isolates were inferred by the Recombination Detection Program (RDP) and varied in the number and location of the recombination events, indicating different evolution origins. Overall, our study highlights the genetic diversity of HAdV-41 isolates circulating in Shanghai, which may have evolved from inter-strain recombination. Nature Publishing Group UK 2017-06-14 /pmc/articles/PMC5471248/ /pubmed/28615624 http://dx.doi.org/10.1038/s41598-017-01293-3 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 Li, Peng Yang, Lang Guo, Jiayin Zou, Wenwei Xu, Xuebin Yang, Xiaoxia Du, Xinying Qiu, Shaofu Song, Hongbin Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title | Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title_full | Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title_fullStr | Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title_full_unstemmed | Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title_short | Circulation of HAdV-41 with diverse genome types and recombination in acute gastroenteritis among children in Shanghai |
title_sort | circulation of hadv-41 with diverse genome types and recombination in acute gastroenteritis among children in shanghai |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471248/ https://www.ncbi.nlm.nih.gov/pubmed/28615624 http://dx.doi.org/10.1038/s41598-017-01293-3 |
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