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Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020

Human enterovirus causes various clinical manifestations in the form of rashes, febrile illness, flu-like illness, uveitis, hand–foot–mouth disease (HFMD), herpangina, meningitis, and encephalitis. Enterovirus A71 and coxsackievirus are significant causes of epidemic HFMD worldwide, especially in ch...

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Autores principales: Sittikul, Pichamon, Batty, Elizabeth M., Yodsawat, Prasert, Nuanpirom, Jiratchaya, Kosoltanapiwat, Nathamon, Sangket, Unitsa, Chatchen, Supawat, Day, Nicholas P. J., Thaipadungpanit, Janjira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301176/
https://www.ncbi.nlm.nih.gov/pubmed/37376696
http://dx.doi.org/10.3390/v15061397
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author Sittikul, Pichamon
Batty, Elizabeth M.
Yodsawat, Prasert
Nuanpirom, Jiratchaya
Kosoltanapiwat, Nathamon
Sangket, Unitsa
Chatchen, Supawat
Day, Nicholas P. J.
Thaipadungpanit, Janjira
author_facet Sittikul, Pichamon
Batty, Elizabeth M.
Yodsawat, Prasert
Nuanpirom, Jiratchaya
Kosoltanapiwat, Nathamon
Sangket, Unitsa
Chatchen, Supawat
Day, Nicholas P. J.
Thaipadungpanit, Janjira
author_sort Sittikul, Pichamon
collection PubMed
description Human enterovirus causes various clinical manifestations in the form of rashes, febrile illness, flu-like illness, uveitis, hand–foot–mouth disease (HFMD), herpangina, meningitis, and encephalitis. Enterovirus A71 and coxsackievirus are significant causes of epidemic HFMD worldwide, especially in children aged from birth to five years old. The enterovirus genotype variants causing HFMD epidemics have been reported increasingly worldwide in the last decade. We aim to use simple and robust molecular tools to investigate human enteroviruses circulating among kindergarten students at genotype and subgenotype levels. With the partial 5′-UTR sequencing analysis as a low-resolution preliminary grouping tool, ten enterovirus A71 (EV-A71) and coxsackievirus clusters were identified among 18 symptomatic cases and 14 asymptomatic cases in five kindergartens in Bangkok, Thailand, between July 2019 and January 2020. Two occurrences of a single clone causing an infection cluster were identified (EV-A71 C1-like subgenotype and coxsackievirus A6). Random amplification-based sequencing using MinION (Oxford Nanopore Technology) helped identify viral transmission between two closely related clones. Diverse genotypes co-circulating among children in kindergartens are reservoirs for new genotype variants emerging, which might be more virulent or better at immune escape. Surveillance of highly contagious enterovirus in communities is essential for disease notifications and controls.
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spelling pubmed-103011762023-06-29 Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020 Sittikul, Pichamon Batty, Elizabeth M. Yodsawat, Prasert Nuanpirom, Jiratchaya Kosoltanapiwat, Nathamon Sangket, Unitsa Chatchen, Supawat Day, Nicholas P. J. Thaipadungpanit, Janjira Viruses Article Human enterovirus causes various clinical manifestations in the form of rashes, febrile illness, flu-like illness, uveitis, hand–foot–mouth disease (HFMD), herpangina, meningitis, and encephalitis. Enterovirus A71 and coxsackievirus are significant causes of epidemic HFMD worldwide, especially in children aged from birth to five years old. The enterovirus genotype variants causing HFMD epidemics have been reported increasingly worldwide in the last decade. We aim to use simple and robust molecular tools to investigate human enteroviruses circulating among kindergarten students at genotype and subgenotype levels. With the partial 5′-UTR sequencing analysis as a low-resolution preliminary grouping tool, ten enterovirus A71 (EV-A71) and coxsackievirus clusters were identified among 18 symptomatic cases and 14 asymptomatic cases in five kindergartens in Bangkok, Thailand, between July 2019 and January 2020. Two occurrences of a single clone causing an infection cluster were identified (EV-A71 C1-like subgenotype and coxsackievirus A6). Random amplification-based sequencing using MinION (Oxford Nanopore Technology) helped identify viral transmission between two closely related clones. Diverse genotypes co-circulating among children in kindergartens are reservoirs for new genotype variants emerging, which might be more virulent or better at immune escape. Surveillance of highly contagious enterovirus in communities is essential for disease notifications and controls. MDPI 2023-06-20 /pmc/articles/PMC10301176/ /pubmed/37376696 http://dx.doi.org/10.3390/v15061397 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sittikul, Pichamon
Batty, Elizabeth M.
Yodsawat, Prasert
Nuanpirom, Jiratchaya
Kosoltanapiwat, Nathamon
Sangket, Unitsa
Chatchen, Supawat
Day, Nicholas P. J.
Thaipadungpanit, Janjira
Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title_full Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title_fullStr Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title_full_unstemmed Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title_short Diversity of Human Enterovirus Co-Circulations in Five Kindergartens in Bangkok between July 2019 and January 2020
title_sort diversity of human enterovirus co-circulations in five kindergartens in bangkok between july 2019 and january 2020
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301176/
https://www.ncbi.nlm.nih.gov/pubmed/37376696
http://dx.doi.org/10.3390/v15061397
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