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dc.contributor.authorScheffer, Camila Menguept_BR
dc.contributor.authorPetzhold, Sylio Alfredopt_BR
dc.contributor.authorVarela, Ana Paula Muterlept_BR
dc.contributor.authorPaim, Willian Pintopt_BR
dc.contributor.authorDuarte, Phelipe Magalhãespt_BR
dc.contributor.authorLoiko, Márcia Reginapt_BR
dc.contributor.authorCerva, Cristinept_BR
dc.contributor.authorSchmidt, Candicept_BR
dc.contributor.authorWendlant, Adriélipt_BR
dc.contributor.authorCibulski, Samuel Paulopt_BR
dc.contributor.authorLima, Diane Alves dept_BR
dc.contributor.authorTochetto, Carolinept_BR
dc.contributor.authorSantos, Anne Caroline Ramos dospt_BR
dc.contributor.authorHerpich, Juliana Inêspt_BR
dc.contributor.authorTeixeira, Thais Fumacopt_BR
dc.contributor.authorSantos, Helton Fernandes dospt_BR
dc.contributor.authorCampos, Fabrício Souzapt_BR
dc.contributor.authorFranco, Ana Claudiapt_BR
dc.contributor.authorRoehe, Paulo Michelpt_BR
dc.date.accessioned2023-03-07T03:25:48Zpt_BR
dc.date.issued2023pt_BR
dc.identifier.issn2306-7381pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/255377pt_BR
dc.description.abstractBovine alphaherpesvirus 1 (subtypes 1.1, 1.2a, and 1.2b), type 5 (subtypes 5a, 5b, and 5c), and bubaline herpesvirus 1 (BuHV-1) induce highly, though not fully cross-reactive serological responses. Most types and subtypes of these viruses circulate particularly in countries of the southern hemisphere, notably Brazil and Argentina. Therefore, the detection of infected animals is important in defining prevention and control strategies, particularly when flocks are destined for international trade. Identification of infected herds is most often achieved by assays that detect antibodies, such as enzyme immunoassays (ELISAs). However, to date, no ELISA has been evaluated in its capacity to detect antibodies to these alphaherpesviruses. Here, an ELISA was developed to detect antibodies to all currently recognized BoAHV-1, BoAHV-5, and BuAHV-1 types/subtypes, and its sensitivity and specificity were determined. Six hundred bovine sera were screened in serum neutralization tests (SN) against the seven viruses. ELISAs prepared with each of the viruses were compared to SN. Subsequently, a combined assay with multiple antigens LISA was prepared by mixing five viral antigens, chosen for their highest sensitivity in the preparative assays. In comparison to SN, the mAgELISA sensitivity was 96.5% with 96.1% specificity (κ = 0.93; PPV = 95.0%; NPV = 97.3%). The findings reveal that the mAgELISA developed here is highly suitable for the detection of antibodies, comparable in sensitivity and specificity to that of SN when performed with all known types and subtypes of bovine and bubaline alphaherpesviruses.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofVeterinary Sciences. Basel. Vol. 10, no. 2 (Feb. 2023), 110, 11 p.pt_BR
dc.rightsOpen Accessen
dc.subjectSerological testen
dc.subjectTécnica de imunoensaio enzimático de multiplicaçãopt_BR
dc.subjectAalphaherpesvirusesen
dc.subjectHerpesvirus bovino 1pt_BR
dc.subjectSorologiapt_BR
dc.subjectSerologyen
dc.subjectNeutralizationen
dc.subjectBovinospt_BR
dc.subjectELISAen
dc.titleAn ELISA to detect antibodies to bovine alphaherpesviruses 1 and 5 and bubaline alphaherpesvirus 1 in cattle serapt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001162473pt_BR
dc.type.originEstrangeiropt_BR


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