Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay

Detalhes bibliográficos
Autor(a) principal: de Sousa, RLM
Data de Publicação: 2000
Outros Autores: Montassier, H. J., Pinto, A. A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1128/CDLI.7.6.940-944.2000
http://hdl.handle.net/11449/39511
Resumo: A liquid phase blocking ELISA (LPB-ELISA) was adapted for the detection and quantification of antibodies to Newcastle disease virus. Sera from vaccinated and unvaccinated commercial flocks of ostriches (Struthio camelus) and rheas (Rhea americana) were tested. The purified and nonpurified virus used as the antigen and the capture and detector antibodies were prepared and standardized for this purpose. The hemagglutination-inhibition (HI) test was regarded as the reference method, the cutoff point for the LPB-ELISA was determined by a two-graph receiver operating characteristic analysis. The LPB-ELISA titers regressed significantly (P < 0.0001) on the HI titers with a high correlation coefficient (r = 0.875). The two tests showed good agreement (<kappa> = 0.82; P < 0.0001), relative sensitivity (90.91%) and specificity (91.18%), and accuracy (91.02%), suggesting that they are interchangeable.
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spelling Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assayA liquid phase blocking ELISA (LPB-ELISA) was adapted for the detection and quantification of antibodies to Newcastle disease virus. Sera from vaccinated and unvaccinated commercial flocks of ostriches (Struthio camelus) and rheas (Rhea americana) were tested. The purified and nonpurified virus used as the antigen and the capture and detector antibodies were prepared and standardized for this purpose. The hemagglutination-inhibition (HI) test was regarded as the reference method, the cutoff point for the LPB-ELISA was determined by a two-graph receiver operating characteristic analysis. The LPB-ELISA titers regressed significantly (P < 0.0001) on the HI titers with a high correlation coefficient (r = 0.875). The two tests showed good agreement (<kappa> = 0.82; P < 0.0001), relative sensitivity (90.91%) and specificity (91.18%), and accuracy (91.02%), suggesting that they are interchangeable.Univ Estadual Paulista, Fac Ciências Agrarias & Vet, Dept Vet Pathol, Lab Virol & Immunol, BR-14870000 São Paulo, BrazilUniv São Paulo, Inst Ciências Biomed, Grad Program Microbiol, BR-05508 São Paulo, BrazilFdn Amparo Pesquisa Estado, São Paulo, BrazilUniv Estadual Paulista, Fac Ciências Agrarias & Vet, Dept Vet Pathol, Lab Virol & Immunol, BR-14870000 São Paulo, BrazilAmer Soc MicrobiologyUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Fdn Amparo Pesquisa Estadode Sousa, RLMMontassier, H. J.Pinto, A. A.2014-05-20T15:30:04Z2014-05-20T15:30:04Z2000-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article940-944application/pdfhttp://dx.doi.org/10.1128/CDLI.7.6.940-944.2000Clinical and Diagnostic Laboratory Immunology. Washington: Amer Soc Microbiology, v. 7, n. 6, p. 940-944, 2000.1071-412Xhttp://hdl.handle.net/11449/3951110.1128/CDLI.7.6.940-944.2000WOS:000167743800016WOS000167743800016.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical and Diagnostic Laboratory Immunologyinfo:eu-repo/semantics/openAccess2024-06-07T13:02:47Zoai:repositorio.unesp.br:11449/39511Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:41:43.049368Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
title Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
spellingShingle Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
de Sousa, RLM
title_short Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
title_full Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
title_fullStr Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
title_full_unstemmed Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
title_sort Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
author de Sousa, RLM
author_facet de Sousa, RLM
Montassier, H. J.
Pinto, A. A.
author_role author
author2 Montassier, H. J.
Pinto, A. A.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Fdn Amparo Pesquisa Estado
dc.contributor.author.fl_str_mv de Sousa, RLM
Montassier, H. J.
Pinto, A. A.
description A liquid phase blocking ELISA (LPB-ELISA) was adapted for the detection and quantification of antibodies to Newcastle disease virus. Sera from vaccinated and unvaccinated commercial flocks of ostriches (Struthio camelus) and rheas (Rhea americana) were tested. The purified and nonpurified virus used as the antigen and the capture and detector antibodies were prepared and standardized for this purpose. The hemagglutination-inhibition (HI) test was regarded as the reference method, the cutoff point for the LPB-ELISA was determined by a two-graph receiver operating characteristic analysis. The LPB-ELISA titers regressed significantly (P < 0.0001) on the HI titers with a high correlation coefficient (r = 0.875). The two tests showed good agreement (<kappa> = 0.82; P < 0.0001), relative sensitivity (90.91%) and specificity (91.18%), and accuracy (91.02%), suggesting that they are interchangeable.
publishDate 2000
dc.date.none.fl_str_mv 2000-11-01
2014-05-20T15:30:04Z
2014-05-20T15:30:04Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1128/CDLI.7.6.940-944.2000
Clinical and Diagnostic Laboratory Immunology. Washington: Amer Soc Microbiology, v. 7, n. 6, p. 940-944, 2000.
1071-412X
http://hdl.handle.net/11449/39511
10.1128/CDLI.7.6.940-944.2000
WOS:000167743800016
WOS000167743800016.pdf
url http://dx.doi.org/10.1128/CDLI.7.6.940-944.2000
http://hdl.handle.net/11449/39511
identifier_str_mv Clinical and Diagnostic Laboratory Immunology. Washington: Amer Soc Microbiology, v. 7, n. 6, p. 940-944, 2000.
1071-412X
10.1128/CDLI.7.6.940-944.2000
WOS:000167743800016
WOS000167743800016.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical and Diagnostic Laboratory Immunology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 940-944
application/pdf
dc.publisher.none.fl_str_mv Amer Soc Microbiology
publisher.none.fl_str_mv Amer Soc Microbiology
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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