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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/1272
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dc.contributor.authorBronzoni, RVM-
dc.contributor.authorFatima, M.-
dc.contributor.authorMontassier, S.-
dc.contributor.authorPereira, G. T.-
dc.contributor.authorGama, NMSQ-
dc.contributor.authorSakai, V-
dc.contributor.authorMontassier, H. J.-
dc.date.accessioned2014-05-20T13:13:30Z-
dc.date.available2014-05-20T13:13:30Z-
dc.date.issued2005-09-01-
dc.identifierhttp://dx.doi.org/10.1089/vim.2005.18.569-
dc.identifier.citationViral Immunology. New Rochelle: Mary Ann Liebert Inc., v. 18, n. 3, p. 569-578, 2005.-
dc.identifier.issn0882-8245-
dc.identifier.urihttp://hdl.handle.net/11449/1272-
dc.description.abstractConcanavalin A-Sandwich ELISA (Con A-S-ELISA) was developed for the detection of infectious bronchitis virus (IBV) or chicken specific anti-viral antibodies. The antigen detection limit for the Con A-S-ELISA was 10(5,1) EID50/mL. Three homologous and four heterologous IBV strains were similarly detected. This assay was highly effective in detecting the virus after infected tissue homogenates were passed once in embryonated chicken eggs, showing a good agreement with virus isolation technique. The Con A-S-ELISA was also used to measure anti-IBV chicken antibodies and showed a high coefficient of correlation (r = 0.85) and an agreement of k = 0.80 with the commercially available Indirect-ELISA. The relative sensitivity and specificity between these two tests were, respectively, 92.86% and 95.65% with an accuracy of 93.39%. Thus, the Con A-S-ELISA proved to be able to detect alternatively homologous and heterologous IBV strains or specific chicken anti-IBV antibodies, using the Con A as capture reagent of this assay.en
dc.format.extent569-578-
dc.language.isoeng-
dc.publisherMary Ann Liebert, Inc.-
dc.sourceWeb of Science-
dc.titleDetection of infectious bronchitis virus and specific anti-viral antibodies using a concanavalin A-Sandwich-ELISAen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionInst Biol-
dc.description.affiliationUniv Estadual Paulista, Fac Ciências Agr & Vet, Dept Vet Pathol, Lab Imunol & Virol, BR-14884900 Jaboticabal, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Fac Ciências Agr & Vet, Dept Ciências Exatas, BR-14884900 Jaboticabal, SP, Brazil-
dc.description.affiliationInst Biol, Bastos, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências Agr & Vet, Dept Vet Pathol, Lab Imunol & Virol, BR-14884900 Jaboticabal, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Fac Ciências Agr & Vet, Dept Ciências Exatas, BR-14884900 Jaboticabal, SP, Brazil-
dc.identifier.doi10.1089/vim.2005.18.569-
dc.identifier.wosWOS:000232733600019-
dc.rights.accessRightsAcesso restrito-
dc.identifier.fileWOS000232733600019.pdf-
dc.relation.ispartofViral Immunology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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