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dc.contributor.authorRodriguez, Ariel
dc.contributor.authorFalcón, Ana María
dc.contributor.authorCuevas, María Teresa
dc.contributor.authorPozo, Francisco
dc.contributor.authorGuerra García, María Susana 
dc.contributor.authorGarcía-Barreno, Blanca
dc.contributor.authorMartínez-Orellana, Pamela
dc.contributor.authorPérez-Breña, Pilar
dc.contributor.authorMontoya, María
dc.contributor.authorMelero, José Antonio
dc.contributor.authorPizarro, Manuel
dc.contributor.authorOrtín, Juan
dc.contributor.authorCasas, Inmaculada
dc.contributor.authorNieto, Amelia
dc.contributor.otherUAM. Departamento de Medicina Preventiva y Salud Pública y Microbiologíaes_ES
dc.date.accessioned2015-06-18T09:46:09Z
dc.date.available2015-06-18T09:46:09Z
dc.date.issued2013-01-17
dc.identifier.citationPlos One 8.1 (2013): e53515en_US
dc.identifier.issn1932-6203 (online)en_US
dc.identifier.urihttp://hdl.handle.net/10486/666900
dc.description.abstractPandemic 2009 H1N1 (pH1N1) influenza viruses caused mild symptoms in most infected patients. However, a greater rate of severe disease was observed in healthy young adults and children without co-morbid conditions. Here we tested whether influenza strains displaying differential virulence could be present among circulating pH1N1 viruses. The biological properties and the genotype of viruses isolated from a patient showing mild disease (M) or from a fatal case (F), both without known co-morbid conditions were compared in vitro and in vivo. The F virus presented faster growth kinetics and stronger induction of cytokines than M virus in human alveolar lung epithelial cells. In the murine model in vivo, the F virus showed a stronger morbidity and mortality than M virus. Remarkably, a higher proportion of mice presenting infectious virus in the hearts, was found in F virus-infected animals. Altogether, the data indicate that strains of pH1N1 virus with enhanced pathogenicity circulated during the 2009 pandemic. In addition, examination of chemokine receptor 5 (CCR5) genotype, recently reported as involved in severe influenza virus disease, revealed that the F virus-infected patient was homozygous for the deleted form of CCR5 receptor (CCR5Δ32)en_US
dc.description.sponsorshipThis work was supported by Instituto de Salud Carlos III (Programa especial de investigación sobre la gripe pándemica GR09/0023, GR09/0040, GR09/ 0039) and Ciber de Enfermedades Respiratoriasen_US
dc.format.extent12 pag.es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherPublic Library of Scienceen_US
dc.relation.ispartofPlos Oneen_US
dc.rights© 2013 Rodriguez et al.es_ES
dc.subject.otherAmino Acidsen_US
dc.subject.otherCellsen_US
dc.subject.otherImmunohistochemistryen_US
dc.subject.otherInfluenzaen_US
dc.subject.otherPandemicsen_US
dc.subject.otherInbred BALB Cen_US
dc.titleCharacterization In vitro and In vivo of a pandemic H1N1 influenza virus from a fatal caseen_US
dc.typearticleen
dc.subject.ecienciaMedicinaes_ES
dc.identifier.doi10.1371/journal.pone.0053515es_ES
dc.identifier.publicationfirstpagee53515es_ES
dc.identifier.publicationissue1es_ES
dc.identifier.publicationlastpagee53515es_ES
dc.identifier.publicationvolume8es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccessen
dc.facultadUAMFacultad de Medicina


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