Longitudinal study on enterovirus A71 and coxsackievirus A16 genotype/subgenotype replacements in hand, foot and mouth disease patients in Thailand, 2000–2017

•This longitudinal study explored the enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) subgenotypic replacements.•Emerging EV-A71 subgenotypes and the duration of circulation was revealed over time.•EV-A71 and CV-A16 are the dominant viruses associated with hand, foot and mouth disease in Th...

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Published inInternational journal of infectious diseases Vol. 80; pp. 84 - 91
Main Authors Noisumdaeng, Pirom, Korkusol, Achareeya, Prasertsopon, Jarunee, Sangsiriwut, Kantima, Chokephaibulkit, Kulkanya, Mungaomklang, Anek, Thitithanyanont, Arunee, Buathong, Rome, Guntapong, Ratigorn, Puthavathana, Pilaipan
Format Journal Article
LanguageEnglish
Published Canada Elsevier Ltd 01.03.2019
Elsevier
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Abstract •This longitudinal study explored the enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) subgenotypic replacements.•Emerging EV-A71 subgenotypes and the duration of circulation was revealed over time.•EV-A71 and CV-A16 are the dominant viruses associated with hand, foot and mouth disease in Thailand. Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000–2017. The complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis. The 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades. This study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development.
AbstractList Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000-2017.BACKGROUNDEnterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000-2017.The complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis.METHODSThe complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis.The 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades.RESULTSThe 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades.This study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development.CONCLUSIONSThis study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development.
•This longitudinal study explored the enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) subgenotypic replacements.•Emerging EV-A71 subgenotypes and the duration of circulation was revealed over time.•EV-A71 and CV-A16 are the dominant viruses associated with hand, foot and mouth disease in Thailand. Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000–2017. The complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis. The 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades. This study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development.
Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000-2017. The complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis. The 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades. This study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development.
Background: Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the Asia-Pacific region. Several strains have emerged, circulated, and faded out over time in recent decades. This study investigated the EV-A71 and CV-A16 circulating strains and replacement of genotypes/subgenotypes in Thailand during the years 2000–2017. Methods: The complete VP1 regions of 92 enteroviruses obtained from 90 HFMD patients, one asymptomatic adult contact case, and one encephalitic case were sequenced and investigated for serotypes, genotypes, and subgenotypes using a phylogenetic analysis. Results: The 92 enterovirus isolates were identified as 67 (72.8%) EV-A71 strains comprising subgenotypes B4, B5, C1, C2, C4a, C4b and C5, and 25 (27.2%) CV-A16 strains comprising subgenotypes B1a and B1b. Genotypic/subgenotypic replacements were evidenced during the study period. EV-A71 B5 and C4a have been the major circulating strains in Thailand for more than a decade, and CV-A16 B1a has been circulating for almost two decades. Conclusions: This study provides chronological data on the molecular epidemiology of EV-A71 and CV-A16 subgenotypes in Thailand. Subgenotypic replacement frequently occurred with EV-A71, but not CV-A16. Monitoring for viral genetic and subgenotypic changes is important for molecular diagnosis, vaccine selection, and vaccine development. Keywords: Hand, foot and mouth disease, Enterovirus A71, Coxsackievirus A16, VP1 sequence, Molecular epidemiology, Genotypic/subgenotypic replacement
Author Mungaomklang, Anek
Prasertsopon, Jarunee
Sangsiriwut, Kantima
Noisumdaeng, Pirom
Chokephaibulkit, Kulkanya
Korkusol, Achareeya
Buathong, Rome
Thitithanyanont, Arunee
Guntapong, Ratigorn
Puthavathana, Pilaipan
Author_xml – sequence: 1
  givenname: Pirom
  surname: Noisumdaeng
  fullname: Noisumdaeng, Pirom
  organization: Faculty of Public Health, Thammasat University (Rangsit Center), Khlong Luang, Pathum Thani 12121, Thailand
– sequence: 2
  givenname: Achareeya
  surname: Korkusol
  fullname: Korkusol, Achareeya
  organization: Department of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok-noi, Bangkok 10700, Thailand
– sequence: 3
  givenname: Jarunee
  surname: Prasertsopon
  fullname: Prasertsopon, Jarunee
  organization: Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakhon Pathom 73170, Thailand
– sequence: 4
  givenname: Kantima
  surname: Sangsiriwut
  fullname: Sangsiriwut, Kantima
  organization: Department of Preventive and Social Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok-noi, Bangkok 10700, Thailand
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  givenname: Kulkanya
  surname: Chokephaibulkit
  fullname: Chokephaibulkit, Kulkanya
  organization: Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok-noi, Bangkok 10700, Thailand
– sequence: 6
  givenname: Anek
  surname: Mungaomklang
  fullname: Mungaomklang, Anek
  organization: Debaratana Nakhon Ratchasima Hospital, Ministry of Public Health, Nakhon Ratchasima 30280, Thailand
– sequence: 7
  givenname: Arunee
  surname: Thitithanyanont
  fullname: Thitithanyanont, Arunee
  organization: Department of Microbiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand
– sequence: 8
  givenname: Rome
  surname: Buathong
  fullname: Buathong, Rome
  organization: Bureau of Epidemiology, Department of Disease Control, Ministry of Public Health, Nonthaburi 11000, Thailand
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  givenname: Ratigorn
  surname: Guntapong
  fullname: Guntapong, Ratigorn
  organization: National Institute of Health, Department of Medical Sciences, Ministry of Public Health, Nonthaburi 11000, Thailand
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  givenname: Pilaipan
  surname: Puthavathana
  fullname: Puthavathana, Pilaipan
  email: pilaipan.put@mahidol.edu
  organization: Department of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok-noi, Bangkok 10700, Thailand
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30639624$$D View this record in MEDLINE/PubMed
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Keywords VP1 sequence
Molecular epidemiology
Hand, foot and mouth disease
Enterovirus A71
Genotypic/subgenotypic replacement
Coxsackievirus A16
Language English
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Snippet •This longitudinal study explored the enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) subgenotypic replacements.•Emerging EV-A71 subgenotypes and the...
Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide, particularly in the...
Background: Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the major causative agents of hand, foot and mouth disease (HFMD) worldwide,...
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StartPage 84
SubjectTerms Coxsackievirus A16
Enterovirus A71
Genotypic/subgenotypic replacement
Hand, foot and mouth disease
Molecular epidemiology
VP1 sequence
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Title Longitudinal study on enterovirus A71 and coxsackievirus A16 genotype/subgenotype replacements in hand, foot and mouth disease patients in Thailand, 2000–2017
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1201971219300141
https://dx.doi.org/10.1016/j.ijid.2018.12.020
https://www.ncbi.nlm.nih.gov/pubmed/30639624
https://www.proquest.com/docview/2179335037
https://doaj.org/article/3133b11f5a0740a5bdc3225c6efcd96b
Volume 80
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