Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/870999
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dc.contributor.authorSEIBERT, C. H.pt_BR
dc.contributor.authorBORSA, M.pt_BR
dc.contributor.authorROSA, R. D.pt_BR
dc.contributor.authorCARGNIN-FERREIRA, E.pt_BR
dc.contributor.authorPEREIRA, A. M. L.pt_BR
dc.contributor.authorGRISARD, E. C.pt_BR
dc.contributor.authorZANETTI, C. R.pt_BR
dc.contributor.authorPINTO, A. R.pt_BR
dc.contributor.otherCAROLINE H. SEIBERT, UNIVERSIDADE FEDERAL DE SANTA CATARINA; MARIANA BORSA, UNIVERSIDADE FEDERAL DE SANTA CATARINA; RAFAEL D. ROSA, UNIVERSIDADE FEDERAL DE SANTA CATARINA; EDUARDO CARGNIN-FERREIRA, UNIVERSIDADE FEDERAL DE SANTA CATARINA; ALITIENE MOURA LEMOS PEREIRA, CPAMN; EDMUNDO C. GRISARD, UNIVERSIDADE FEDERAL DE SANTA CATARINA; CARLOS R. ZANETTI, UNIVERSIDADE FEDERAL DE SANTA CATARINA; AGUINALDO R. PINTO, UNIVERSIDADE FEDERAL DE SANTA CATARINA.pt_BR
dc.date.accessioned2011-04-09T19:01:04Z-
dc.date.available2011-04-09T19:01:04Z-
dc.date.created2010pt_BR
dc.date.issued2010-12-28pt_BR
dc.identifier.other24739pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/870999pt_BR
dc.descriptionInfectious myonecrosis virus (IMNV) has been causing a progressive disease in farm-reared shrimps in Brazil and Indonesia. Immunodiagnosticmethods for IMNVdetection, although reliable, are not employed currently becausemonoclonal antibodies (MAbs) against this virus are not available. In this study, a fragment of the IMNVmajor capsid protein gene, comprising amino acids 300?527 (IMNV300?527),was cloned and expressed in Escherichia coli. The nucleotide sequence of the recombinant IMNV300?527 fragment displayed a high degree of identity to the major capsid protein of IMNV isolates from Brazil (99%) and Indonesia (98%). Ten MAbs were generated against the expressed fragment, and eight of these, mostly IgG2a or IgG2b,were able to bind to IMNVin tissue extracts fromshrimps infected naturally in immunodotblot assays. Six of these MAbs recognized a ?100 kDa protein in a Western-blot, which is the predicted mass of IMNV major capsid protein, and also bound to viral inclusions present in muscle ?broses and in coagulativemyonecrosis, as demonstrated by immunohistochemistry. Among all thoseMAbs created, four did not cross-react with non-infected shrimp tissues; this observation supports their applicability as a sensitive and speci?c immunodiagnosis of IMNV infection in shrimps.pt_BR
dc.description.uribitstream/item/24511/1/JOURNAL.pdfpt_BR
dc.languageenpt_BR
dc.publisherJournal of Virological Methods, Amsterdam-Holanda, v. 169, n. 1, p. 169-175, 2010.pt_BR
dc.relation.ispartofEmbrapa Meio-Norte - Artigo em periódico indexado (ALICE)pt_BR
dc.rightsopenAccesspt_BR
dc.subjectVírus da mionecrose infecciosapt_BR
dc.subjectProteína recombinante.pt_BR
dc.titleDetection of major capsid protein of infectious myonecrosis virus in shrimps using monoclonal antibodies.pt_BR
dc.typeArtigo em periódico indexado (ALICE)pt_BR
dc.date.updated2011-04-10T11:11:11Zpt_BR
dc.description.version2010pt_BR
dc.subject.thesagroAnticorpo Monoclonalpt_BR
dc.subject.thesagroCamarão.pt_BR
dc.ainfo.id870999pt_BR
dc.ainfo.lastupdate2010-12-28pt_BR
dc.ainfo.depositanteCarga automáticapt_BR
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