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Resumen
The novel Equine Parvovirus-Hepatitis (EqPV-H) was first identified in the serum and liver of a horse that died of equine serum hepatitis, also known as Theiler's disease. Several reports in recent years strongly suggest that EqPV-H is the etiologic agent of Theiler's disease. Brazil is the only South American country where infection with this virus has been reported. This study investigated the presence of EqPV-H DNA in horse serum pools (n=51), [ver mas...]
dc.contributor.authorOlguin Perglione, Cecilia
dc.contributor.authorPolitzki, Romina Paula
dc.contributor.authorAlvarez, Irene
dc.contributor.authorRuiz, Vanesa
dc.coverage.spatialArgentina .......... (nation) (World, South America)es_AR
dc.coverage.spatial7006477es_AR
dc.date.accessioned2024-07-29T10:38:21Z
dc.date.available2024-07-29T10:38:21Z
dc.date.issued2024-07
dc.identifier.issn1090-0233
dc.identifier.otherhttps://doi.org/10.1016/j.tvjl.2024.106204
dc.identifier.urihttp://hdl.handle.net/20.500.12123/18692
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S1090023324001436
dc.description.abstractThe novel Equine Parvovirus-Hepatitis (EqPV-H) was first identified in the serum and liver of a horse that died of equine serum hepatitis, also known as Theiler's disease. Several reports in recent years strongly suggest that EqPV-H is the etiologic agent of Theiler's disease. Brazil is the only South American country where infection with this virus has been reported. This study investigated the presence of EqPV-H DNA in horse serum pools (n=51), commercial horse serum batches (n=5) and individual serum samples from donor horses (n=175) from Argentina. All serum samples were analyzed by quantitative polymerase chain reaction (qPCR) and samples with positive or indeterminate results were further analyzed by NS1 nested-PCR for phylogenetic studies. None of the serum pools was positive by qPCR but 9/51 pools were indeterminate (one or both test sample’s Ct values were higher than the limit of detection). The NS1 nested-PCR detected the EqPV-H DNA in 8 of these indeterminate samples (15.7 % of serum pools). Three of the commercial horse serum batches (60 %) contained EqPV-H DNA, detected either by qPCR and/or nested-PCR. From the 175 individual horse serum samples, three (1.71 %) were positive for EqPV-H by both techniques. The genetic analysis of the 12 partial NS1 sequences obtained showed that the local isolates were similar to EqPV-H sequences from Germany and China. This study provides the first evidence of the presence of EqPV-H in horses and in horse sera commercially available in Argentina and emphasizes the importance of controlling the biosecurity of commercial equine sera as well as any other blood-derived biological products of equine origin.eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherElsevieres_AR
dc.relationinfo:eu-repo/semantics/reference/hdl/20.500.12123/18696
dc.relationinfo:eu-repograntAgreement/INTA/2023-PD-L06-I114, Desarrollo y aplicación de métodos diagnósticos y epidemiológicos para la producción pecuaria sustentable y agroalimentaria en humanos con foco en Una Salud
dc.rightsinfo:eu-repo/semantics/restrictedAccesseng
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/eng
dc.sourceVeterinary journal 306 : 106204. (22 July 2024)es_AR
dc.subjectHorseseng
dc.subjectCaballoes_AR
dc.subjectAnimal Diseaseseng
dc.subjectEnfermedades de los Animaleses_AR
dc.subjectParvoviridaees_AR
dc.subjectHepatitises_AR
dc.subjectFilogeniaes_AR
dc.subjectPhylogenyeng
dc.subjectArgentinaes_AR
dc.subject.otherEquine Parvovirus-Hepatitiseng
dc.subject.otherParvovirus Equino Hepatitises_AR
dc.subject.otherSerum Poolseng
dc.titleFirst report of Equine Parvovirus-Hepatitis (EqPV-H) in Argentinaes_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articleeng
dc.typeinfo:eu-repo/semantics/publishedVersioneng
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)eng
dc.description.origenInstituto de Virologíaes_AR
dc.description.filFil: Olguin Perglione, Cecilia. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Olguin Perglione, Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Politzki, Romina Paula. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Politzki, Romina Paula. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Alvarez, Irene. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Alvarez, Irene. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Ruiz, Vanesa. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.description.filFil: Ruiz, Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Virología e Innovaciones Tecnológicas. Laboratorio de Virus Adventicios (IVIT); Argentinaes_AR
dc.subtypecientifico


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