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Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China
BACKGROUND: Hand, foot and mouth disease (HFMD) is caused by a variety of enterovirus serotypes and the etiological spectrum worldwide has changed since a large scale of outbreaks occurred in 1997. METHODS: A large number of clinical specimens of HFMD patients were collected in Xiangyang and genotyp...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611921/ https://www.ncbi.nlm.nih.gov/pubmed/34819054 http://dx.doi.org/10.1186/s12920-021-01107-6 |
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author | Yu, Yuting Luo, Zhiyu Jin, Weiping Mai, Jianyi Qian, Shasha Lu, Jia Wei, Zhenni Meng, Shengli Wang, Zejun Guan, Xuhua Tong, Yeqing Shen, Shuo |
author_facet | Yu, Yuting Luo, Zhiyu Jin, Weiping Mai, Jianyi Qian, Shasha Lu, Jia Wei, Zhenni Meng, Shengli Wang, Zejun Guan, Xuhua Tong, Yeqing Shen, Shuo |
author_sort | Yu, Yuting |
collection | PubMed |
description | BACKGROUND: Hand, foot and mouth disease (HFMD) is caused by a variety of enterovirus serotypes and the etiological spectrum worldwide has changed since a large scale of outbreaks occurred in 1997. METHODS: A large number of clinical specimens of HFMD patients were collected in Xiangyang and genotyping was performed by qRT-PCR, conventional PCR amplification and sequencing. Among the 146 CV-A5 detected cases, the complete genome sequences of representative strains were determined for genotyping and for recombination analysis. RESULTS: It was found that CV-A5 was one of the six major serotypes that caused the epidemic from October 2016 to December 2017. Phylogenetic analyses based on the VP1 sequences showed that these CV-A5 belonged to the genotype D which dominantly circulated in China. Recombination occurred between the CV-A5 and CV-A2 strains with a breakpoint in the 2A region at the nucleotide 3791. CONCLUSIONS: The result may explain the emergence of CV-A5 as one of the major pathogens of HFMD. A multivalent vaccine against HFMD is urgently needed to control the disease and to prevent emerging and spreading of new recombinants. |
format | Online Article Text |
id | pubmed-8611921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86119212021-11-29 Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China Yu, Yuting Luo, Zhiyu Jin, Weiping Mai, Jianyi Qian, Shasha Lu, Jia Wei, Zhenni Meng, Shengli Wang, Zejun Guan, Xuhua Tong, Yeqing Shen, Shuo BMC Med Genomics Research Article BACKGROUND: Hand, foot and mouth disease (HFMD) is caused by a variety of enterovirus serotypes and the etiological spectrum worldwide has changed since a large scale of outbreaks occurred in 1997. METHODS: A large number of clinical specimens of HFMD patients were collected in Xiangyang and genotyping was performed by qRT-PCR, conventional PCR amplification and sequencing. Among the 146 CV-A5 detected cases, the complete genome sequences of representative strains were determined for genotyping and for recombination analysis. RESULTS: It was found that CV-A5 was one of the six major serotypes that caused the epidemic from October 2016 to December 2017. Phylogenetic analyses based on the VP1 sequences showed that these CV-A5 belonged to the genotype D which dominantly circulated in China. Recombination occurred between the CV-A5 and CV-A2 strains with a breakpoint in the 2A region at the nucleotide 3791. CONCLUSIONS: The result may explain the emergence of CV-A5 as one of the major pathogens of HFMD. A multivalent vaccine against HFMD is urgently needed to control the disease and to prevent emerging and spreading of new recombinants. BioMed Central 2021-11-24 /pmc/articles/PMC8611921/ /pubmed/34819054 http://dx.doi.org/10.1186/s12920-021-01107-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Yu, Yuting Luo, Zhiyu Jin, Weiping Mai, Jianyi Qian, Shasha Lu, Jia Wei, Zhenni Meng, Shengli Wang, Zejun Guan, Xuhua Tong, Yeqing Shen, Shuo Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title | Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title_full | Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title_fullStr | Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title_full_unstemmed | Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title_short | Emergence of a novel recombinant of CV-A5 in HFMD epidemics in Xiangyang, China |
title_sort | emergence of a novel recombinant of cv-a5 in hfmd epidemics in xiangyang, china |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611921/ https://www.ncbi.nlm.nih.gov/pubmed/34819054 http://dx.doi.org/10.1186/s12920-021-01107-6 |
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