Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand

Enterovirus A71 (EV-A71) can cause hand, foot, and mouth disease (HFMD) in children and may be associated with severe neurological complications. There have been numerous reports of increased incidence of EV-A71 subgenogroup C1 (EV-A71 C1) infections associated with neurological diseases since the f...

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Main Authors: Jiratchaya Puenpa, Kamol Suwannakarn, Jira Chansaenroj, Chompoonut Auphimai, Nasamon Wanlapakorn, Sompong Vongpunsawad, Yong Poovorawan
Other Authors: Siriraj Hospital
Format: Article
Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/77250
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spelling th-mahidol.772502022-08-04T15:49:01Z Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand Jiratchaya Puenpa Kamol Suwannakarn Jira Chansaenroj Chompoonut Auphimai Nasamon Wanlapakorn Sompong Vongpunsawad Yong Poovorawan Siriraj Hospital Chulalongkorn University Immunology and Microbiology Enterovirus A71 (EV-A71) can cause hand, foot, and mouth disease (HFMD) in children and may be associated with severe neurological complications. There have been numerous reports of increased incidence of EV-A71 subgenogroup C1 (EV-A71 C1) infections associated with neurological diseases since the first occurrence in Germany in 2015. Here, we describe 11 full-length genome sequences of 2019 EV-A71 C1 strains isolated from HFMD patients in Thailand from 2019 to early 2020. The genetic evolution of 2019 EV-A71 C1 was traced in the outbreaks, and the emergence of multiple lineages was detected. Our results demonstrated that 2019 EV-A71 C1 from Thailand emerged through recombination between its nonstructural protein gene and those of other EV-A genotypes. Bayesian-based phylogenetic analysis showed that the 2019 EV-A71 C1 Thai strains share a common ancestor with variants in Europe (Denmark and France). The substitution rate for the 2019 EV-A71 C1 genome was estimated to be 4.38 × 10−3 substitutions/(site∙year−1) (95% highest posterior density interval: 3.84–4.94 × 10−3 substitutions/[site∙year−1]), approximating that observed between previous EV-A71 C1 outbreaks. These data are essential for understanding the evolution of EV-A C1 during the ongoing HFMD outbreak and may be relevant to disease outcomes in children worldwide. 2022-08-04T08:49:01Z 2022-08-04T08:49:01Z 2021-08-01 Article Archives of Virology. Vol.166, No.8 (2021), 2209-2216 10.1007/s00705-021-05130-x 14328798 03048608 2-s2.0-85107140826 https://repository.li.mahidol.ac.th/handle/123456789/77250 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85107140826&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Immunology and Microbiology
spellingShingle Immunology and Microbiology
Jiratchaya Puenpa
Kamol Suwannakarn
Jira Chansaenroj
Chompoonut Auphimai
Nasamon Wanlapakorn
Sompong Vongpunsawad
Yong Poovorawan
Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
description Enterovirus A71 (EV-A71) can cause hand, foot, and mouth disease (HFMD) in children and may be associated with severe neurological complications. There have been numerous reports of increased incidence of EV-A71 subgenogroup C1 (EV-A71 C1) infections associated with neurological diseases since the first occurrence in Germany in 2015. Here, we describe 11 full-length genome sequences of 2019 EV-A71 C1 strains isolated from HFMD patients in Thailand from 2019 to early 2020. The genetic evolution of 2019 EV-A71 C1 was traced in the outbreaks, and the emergence of multiple lineages was detected. Our results demonstrated that 2019 EV-A71 C1 from Thailand emerged through recombination between its nonstructural protein gene and those of other EV-A genotypes. Bayesian-based phylogenetic analysis showed that the 2019 EV-A71 C1 Thai strains share a common ancestor with variants in Europe (Denmark and France). The substitution rate for the 2019 EV-A71 C1 genome was estimated to be 4.38 × 10−3 substitutions/(site∙year−1) (95% highest posterior density interval: 3.84–4.94 × 10−3 substitutions/[site∙year−1]), approximating that observed between previous EV-A71 C1 outbreaks. These data are essential for understanding the evolution of EV-A C1 during the ongoing HFMD outbreak and may be relevant to disease outcomes in children worldwide.
author2 Siriraj Hospital
author_facet Siriraj Hospital
Jiratchaya Puenpa
Kamol Suwannakarn
Jira Chansaenroj
Chompoonut Auphimai
Nasamon Wanlapakorn
Sompong Vongpunsawad
Yong Poovorawan
format Article
author Jiratchaya Puenpa
Kamol Suwannakarn
Jira Chansaenroj
Chompoonut Auphimai
Nasamon Wanlapakorn
Sompong Vongpunsawad
Yong Poovorawan
author_sort Jiratchaya Puenpa
title Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
title_short Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
title_full Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
title_fullStr Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
title_full_unstemmed Genetic diversity and evolution of enterovirus A71 subgenogroup C1 from children with hand, foot, and mouth disease in Thailand
title_sort genetic diversity and evolution of enterovirus a71 subgenogroup c1 from children with hand, foot, and mouth disease in thailand
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/77250
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