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dc.contributor.authorRungnapa Malasaoen_US
dc.contributor.authorPattara Khamrinen_US
dc.contributor.authorKattareeya Kumthipen_US
dc.contributor.authorHiroshi Ushijimaen_US
dc.contributor.authorNiwat Maneekarnen_US
dc.date.accessioned2019-08-05T04:38:06Z-
dc.date.available2019-08-05T04:38:06Z-
dc.date.issued2019-07-01en_US
dc.identifier.issn03048608en_US
dc.identifier.other2-s2.0-85067052401en_US
dc.identifier.other10.1007/s00705-019-04249-2en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067052401&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/65644-
dc.description.abstract© 2019, Springer-Verlag GmbH Austria, part of Springer Nature. Little is known about human parechovirus (HPeV) infection in Thailand. The genotype distribution of HPeV strains in children admitted to hospitals with acute gastroenteritis was investigated using polymerase chain reaction (PCR) and nucleotide sequencing of the VP1 region as the detection and genotype identification methods, respectively. Of a total of 2,002 stool samples, 49 (2.4%) were positive for HPeV. Of these, HPeV-1 was the most predominant genotype (40.8%), followed by HPeV-3 (16.3%) and HPeV-14 (16.3%), while HPeV-5, -6, -2, -4, and -8 strains were less frequently detected, at 10.2%, 8.2%, 2%, 2%, and 2%, respectively. HPeV infections were detected throughout the year with the biannual peaks of infection in the rainy (Jun-Jul-Aug) and winter (Nov-Dec-Jan) months in Thailand. Based on VP1 amino acid sequence alignment, the arginyl-glycyl-aspartic acid (RGD) motif was found in HPeV-1, -2, -4, and -6 strains. Additionally, an amino acid insertion at the N-terminus of VP1 was observed in HPeV-4 and HPeV-5 strains. Phylogenetic analysis revealed that small clades of HPeV-1 and HPeV-3 strains emerged in 2016 and 2015, respectively, and dominated in the year of their emergence. The HPeV strains detected in Thailand in this study were most closely related to reference strains from Asia and Europe. The evolutionary rate of HPeV strains was 2.87 × 10−4 (95% highest posterior density (HPD) 0.10-6.14 × 10−4) substitutions/site/year. These findings provide information about the genetic diversity and evolutionary dynamics of HPeV genotypes circulating in pediatric patients with acute gastroenteritis in Thailand.en_US
dc.subjectImmunology and Microbiologyen_US
dc.titleMolecular epidemiology and genetic diversity of human parechoviruses in children hospitalized with acute diarrhea in Thailand during 2011-2016en_US
dc.typeJournalen_US
article.title.sourcetitleArchives of Virologyen_US
article.volume164en_US
article.stream.affiliationsNihon University School of Medicineen_US
article.stream.affiliationsChiang Mai Universityen_US
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