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dc.contributor.authorBarral, Thiago Doria
dc.contributor.authorInfantes-Lorenzo, José A.
dc.contributor.authorMoreno, Inmaculada
dc.contributor.authorde Garnica García, M. Gracia
dc.contributor.authorPérez de Val, Bernat
dc.contributor.authorGortázar, Christian
dc.contributor.authorMeyer, Roberto
dc.contributor.authorPortela, Ricardo D.
dc.contributor.authorDomínguez, Lucas
dc.contributor.authorDomínguez, Mercedes
dc.contributor.authorBalseiro, Ana
dc.contributor.otherProducció Animalca
dc.date.accessioned2023-02-08T18:08:27Z
dc.date.available2023-10-07T22:45:20Z
dc.date.issued2022-10-07
dc.identifier.citationBarral, Thiago Doria, José A. Infantes-Lorenzo, Inmaculada Moreno, M. Gracia de Garnica García, Bernat Pérez de Val, Christian Gortázar, and Roberto Meyer et al. 2022. "P22 Protein Complex In The Serodiagnosis Of Animal Tuberculosis: Antigenic Stability And Cross-Reactivity With Corynebacterium Pseudotuberculosis Infection". Comparative Immunology, Microbiology And Infectious Diseases 90-91: 101891. doi:10.1016/j.cimid.2022.101891.ca
dc.identifier.issn0147-9571ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/2048
dc.description.abstractThe P22 ELISA was recently developed for the serodiagnosis of animal tuberculosis. Herein, the stability of the P22 antigen in different presentations and storage conditions, and the cross-reactivity with Corynebacterium pseudotuberculosis infection in small ruminants were evaluated. For the stability assay, serum samples from cows, sheep, goats, alpacas, badgers, and wild boar were used in the P22 ELISA. The cross-reactivity analysis used sera from sheep and goats with caseous lymphadenitis (CLA). Differences in the immune recognition of P22 were found when the antigen was stored at 40 °C, but without altering the negative or positive status of each sample. P22 ELISA presented 5.71 % cross-reactivity when CLA-positive sheep were evaluated, but no cross-reaction was observed among CLA-positive goat serum samples. This study showed that the P22 protein complex is stable under different formulations and temperatures, and that the assay presents a low cross-reactivity with CLA.ca
dc.format.extent26ca
dc.language.isoengca
dc.publisherElsevierca
dc.relation.ispartofComparative Immunology, Microbiology and Infectious Diseasesca
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleP22 protein complex in the serodiagnosis of animal tuberculosis: Antigenic stability and cross-reactivity with Corynebacterium pseudotuberculosis infectionca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/acceptedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.relation.projectIDMICIU-FEDER/Programa Estatal de I+D+I orientada a los retos de la sociedad/RTI2018-096010-B-C21/ES/El tejón (Meles meles) y la tuberculosis animal en España: interacción tejón-bovino en hospot areas y medidas de control de la enfermedad en la interfase/ca
dc.subject.udc619ca
dc.identifier.doihttps://doi.org/10.1016/j.cimid.2022.101891ca
dc.contributor.groupSanitat Animalca


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