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dc.contributor.authorArana, Ainara
dc.contributor.authorCilla Eguiluz, Carlos Gustavo
dc.contributor.authorMontes, Milagrosa
dc.contributor.authorGomariz, María
dc.contributor.authorPérez Trallero, Emilio
dc.date.accessioned2016-01-04T13:12:06Z
dc.date.available2016-01-04T13:12:06Z
dc.date.issued2014-06-03
dc.identifier.citationPLOS ONE 9(6) : (2014) // Article ID e98875es
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/16582
dc.description.abstractBackground: Noroviruses (NoVs) are genetically diverse, with genogroup II-and within it-genotype 4 (GII.4) being the most prevalent cause of acute gastroenteritis worldwide. The aim of this study was to characterize genogroup II NoV causing acute gastroenteritis in the Basque Country (northern Spain) from 2009-2012. Methods: The presence of NoV RNA was investigated by reverse transcriptase-polymerase chain reaction (RT-PCR) in stool specimens from children younger than 15 years old with community-acquired acute gastroenteritis, and from hospitalized adults or elderly residents of nursing homes with acute gastroenteritis. For genotyping, the open reading frames ORF1 (encoding the polymerase) and ORF2 (encoding the major capsid protein) were partially amplified and sequenced. Recombinant strains were confirmed by PCR of the ORF1/ORF2 junction region. Results: NoV was detected in 16.0% (453/2826) of acute gastroenteritis episodes in children younger than 2 years, 9.9% (139/1407) in children from 2 to 14 years, and 35.8% (122/341) in adults. Of 317 NoVs characterized, 313 were genogroup II and four were genogroup I. The GII.4 variants Den Haag-2006b and New Orleans-2009 predominated in 2009 and 2010-2011, respectively. In 2012, the New Orleans-2009 variant was partially replaced by the Sydney-2012 variant (GII.Pe/GII.4) and New Orleans-2009/Sydney-2012 recombinant strains. The predominant capsid genotype in all age groups was GII.4, which was the only genotype detected in outbreaks. The second most frequent genotype was GII.3 (including the recently described recombination GII.P16/GII.3), which was detected almost exclusively in children. Conclusion: Nine different genotypes of NoV genogroup II were detected; among these, intergenotype recombinant strains represented an important part, highlighting the role of recombination in the evolution of NoVs. Detection of new NoV strains, not only GII.4 strains, shortly after their first detection in other parts of the world shows that many NoV strains can spread rapidly.es
dc.description.sponsorshipThis work was partly funded by a grant from the Basque Country Government to the University Research Groups (grant IT656-13). Ainara Arana is supported by a grant for the training of predoctoral researchers, Basque Government, San Sebastian, Spain; grant PRE-2013-2-319. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es
dc.language.isoenges
dc.publisherPublic Library Sciencees
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectmolecular epidemiologyes
dc.subjectacute gastroenteritises
dc.subjectsporadic gastroenteritises
dc.subjectchildrenes
dc.subjectoutbreakses
dc.subjectevolutiones
dc.subjectstrainses
dc.subjectsurveillancees
dc.subjectprevalencees
dc.subjectinfectiones
dc.titleGenotypes, Recombinant Forms, and Variants of Norovirus GII.4 in Gipuzkoa (Basque Country, Spain), 2009-2012es
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder2014 Arana et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.relation.publisherversionhttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098875#abstract0es
dc.identifier.doi10.1371/journal.pone.0098875
dc.departamentoesMedicina preventiva y salud públicaes_ES
dc.departamentoeuPrebentzio medikuntza eta osasun publikoaes_ES
dc.subject.categoriaAGRICULTURAL AND BIOLOGICAL SCIENCES
dc.subject.categoriaMEDICINE
dc.subject.categoriaBIOCHEMISTRY AND MOLECULAR BIOLOGY


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