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dc.contributor.authorKanittapon Supadejen_US
dc.contributor.authorPattara Khamrinen_US
dc.contributor.authorKattareeya Kumthipen_US
dc.contributor.authorRungnapa Malasaoen_US
dc.contributor.authorNatthawan Chaimongkolen_US
dc.contributor.authorMayuko Saitoen_US
dc.contributor.authorHitoshi Oshitanien_US
dc.contributor.authorHiroshi Ushijimaen_US
dc.contributor.authorNiwat Maneekarnen_US
dc.date.accessioned2018-11-29T07:45:24Z-
dc.date.available2018-11-29T07:45:24Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn10969071en_US
dc.identifier.issn01466615en_US
dc.identifier.other2-s2.0-85055154361en_US
dc.identifier.other10.1002/jmv.25261en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055154361&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62747-
dc.description.abstract© 2018 Wiley Periodicals, Inc. Norovirus (NoV) and sapovirus (SaV) are recognized as the causative agents of acute gastroenteritis, and NoV is one of the leading pathogens reported worldwide. This study reports on the distribution of NoV and SaV genotypes in children hospitalized with acute gastroenteritis in Chiang Mai, Thailand, from January 2015 to February 2017. From a total of 843 stool samples, 170 (20.2%) and 16 (1.9%) were identified as having NoV and SaV infections, respectively. Two samples (0.2%) were positive for both NoV and SaV. Of these, NoV GII.4 (57.2%) was the dominant genotype, followed by GII.2, GII.3, GII.17, GII.6, GII.7, GII.13, GII.14, GII.15, GII.21, GI.6, and GI.5. Among the NoV GII.4 variants, Sydney 2012 was the dominant variant during the period 2015-2016, while the other variants detected in this study were Asia 2003 and New Orleans 2009. Interestingly, an increase of NoV GII.2 was observed in 2016 and 2017. Characterization of partial RNA-dependent RNA polymerase and VP1 nucleotide sequences of GII.2 strains revealed that more than half of the GII.2 strains circulating in 2016 and 2017 were recombinant strains of GII.P16/GII.2. For SaV, the majority of strains belonged to GI.1 (55.6%) and GI.2 (33.3%), while GII.5 accounted for 11.1%. In conclusion, this study demonstrates the diversity of NoV and SaV, and the emergence of NoV GII.P16/GII.2 recombinant strains in 2016 and 2017 in Chiang Mai, Thailand.en_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleDistribution of norovirus and sapovirus genotypes with emergence of NoV GII.P16/GII.2 recombinant strains in Chiang Mai, Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Medical Virologyen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsTohoku University School of Medicineen_US
article.stream.affiliationsNihon University School of Medicineen_US
article.stream.affiliationsUniversity of Tokyoen_US
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