Cargando…
Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019
BACKGROUND: Coxsackievirus A16 (CVA16) is one of the major etiological agents of hand, foot and mouth disease (HFMD). This study aimed to investigate the molecular epidemiology and evolutionary characteristics of CVA16. METHODS: Throat swabs were collected from children with HFMD and suspected HFMD...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523403/ https://www.ncbi.nlm.nih.gov/pubmed/34453285 http://dx.doi.org/10.1007/s12519-021-00451-y |
_version_ | 1784585293175717888 |
---|---|
author | Hu, Ya-Fang Jia, Li-Ping Yu, Fang-Yuan Liu, Li-Ying Song, Qin-Wei Dong, Hui-Jin Deng, Jie Qian, Yuan Zhao, Lin-Qing Deng, Li Huang, Hui Zhu, Ru-Nan |
author_facet | Hu, Ya-Fang Jia, Li-Ping Yu, Fang-Yuan Liu, Li-Ying Song, Qin-Wei Dong, Hui-Jin Deng, Jie Qian, Yuan Zhao, Lin-Qing Deng, Li Huang, Hui Zhu, Ru-Nan |
author_sort | Hu, Ya-Fang |
collection | PubMed |
description | BACKGROUND: Coxsackievirus A16 (CVA16) is one of the major etiological agents of hand, foot and mouth disease (HFMD). This study aimed to investigate the molecular epidemiology and evolutionary characteristics of CVA16. METHODS: Throat swabs were collected from children with HFMD and suspected HFMD during 2010–2019. Enteroviruses (EVs) were detected and typed by real-time reverse transcription-polymerase chain reaction (RT-PCR) and RT-PCR. The genotype, evolutionary rate, the most recent common ancestor, population dynamics and selection pressure of CVA16 were analyzed based on viral protein gene (VP1) by bioinformatics software. RESULTS: A total of 4709 throat swabs were screened. EVs were detected in 3180 samples and 814 were CVA16 positive. More than 81% of CVA16-positive children were under 5 years old. The prevalence of CVA16 showed obvious periodic fluctuations with a high level during 2010–2012 followed by an apparent decline during 2013–2017. However, the activities of CVA16 increased gradually during 2018–2019. All the Beijing CVA16 strains belonged to sub-genotype B1, and B1b was the dominant strain. One B1c strain was detected in Beijing for the first time in 2016. The estimated mean evolutionary rate of VP1 gene was 4.49 × 10(–3) substitution/site/year. Methionine gradually fixed at site-23 of VP1 since 2012. Two sites were detected under episodic positive selection, one of which (site-223) located in neutralizing linear epitope PEP71. CONCLUSIONS: The dominant strains of CVA16 belonged to clade B1b and evolved in a fast evolutionary rate during 2010–2019 in Beijing. To provide more favorable data for HFMD prevention and control, it is necessary to keep attention on molecular epidemiological and evolutionary characteristics of CVA16. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-021-00451-y. |
format | Online Article Text |
id | pubmed-8523403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-85234032021-10-22 Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 Hu, Ya-Fang Jia, Li-Ping Yu, Fang-Yuan Liu, Li-Ying Song, Qin-Wei Dong, Hui-Jin Deng, Jie Qian, Yuan Zhao, Lin-Qing Deng, Li Huang, Hui Zhu, Ru-Nan World J Pediatr Original Article BACKGROUND: Coxsackievirus A16 (CVA16) is one of the major etiological agents of hand, foot and mouth disease (HFMD). This study aimed to investigate the molecular epidemiology and evolutionary characteristics of CVA16. METHODS: Throat swabs were collected from children with HFMD and suspected HFMD during 2010–2019. Enteroviruses (EVs) were detected and typed by real-time reverse transcription-polymerase chain reaction (RT-PCR) and RT-PCR. The genotype, evolutionary rate, the most recent common ancestor, population dynamics and selection pressure of CVA16 were analyzed based on viral protein gene (VP1) by bioinformatics software. RESULTS: A total of 4709 throat swabs were screened. EVs were detected in 3180 samples and 814 were CVA16 positive. More than 81% of CVA16-positive children were under 5 years old. The prevalence of CVA16 showed obvious periodic fluctuations with a high level during 2010–2012 followed by an apparent decline during 2013–2017. However, the activities of CVA16 increased gradually during 2018–2019. All the Beijing CVA16 strains belonged to sub-genotype B1, and B1b was the dominant strain. One B1c strain was detected in Beijing for the first time in 2016. The estimated mean evolutionary rate of VP1 gene was 4.49 × 10(–3) substitution/site/year. Methionine gradually fixed at site-23 of VP1 since 2012. Two sites were detected under episodic positive selection, one of which (site-223) located in neutralizing linear epitope PEP71. CONCLUSIONS: The dominant strains of CVA16 belonged to clade B1b and evolved in a fast evolutionary rate during 2010–2019 in Beijing. To provide more favorable data for HFMD prevention and control, it is necessary to keep attention on molecular epidemiological and evolutionary characteristics of CVA16. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12519-021-00451-y. Springer Singapore 2021-08-28 2021 /pmc/articles/PMC8523403/ /pubmed/34453285 http://dx.doi.org/10.1007/s12519-021-00451-y 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/) . |
spellingShingle | Original Article Hu, Ya-Fang Jia, Li-Ping Yu, Fang-Yuan Liu, Li-Ying Song, Qin-Wei Dong, Hui-Jin Deng, Jie Qian, Yuan Zhao, Lin-Qing Deng, Li Huang, Hui Zhu, Ru-Nan Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title | Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title_full | Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title_fullStr | Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title_full_unstemmed | Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title_short | Molecular epidemiology of coxsackievirus A16 circulating in children in Beijing, China from 2010 to 2019 |
title_sort | molecular epidemiology of coxsackievirus a16 circulating in children in beijing, china from 2010 to 2019 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523403/ https://www.ncbi.nlm.nih.gov/pubmed/34453285 http://dx.doi.org/10.1007/s12519-021-00451-y |
work_keys_str_mv | AT huyafang molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT jialiping molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT yufangyuan molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT liuliying molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT songqinwei molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT donghuijin molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT dengjie molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT qianyuan molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT zhaolinqing molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT dengli molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT huanghui molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 AT zhurunan molecularepidemiologyofcoxsackievirusa16circulatinginchildreninbeijingchinafrom2010to2019 |