Detection and quantification of antibodies to Newcastle disease virus in ostrich and rhea sera using a liquid phase blocking enzyme-linked immunosorbent assay
Autor(a) principal: | |
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Data de Publicação: | 2000 |
Outros Autores: | , |
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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Repositório Institucional da UNESP |
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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 |
|
_version_ |
1808129234641616896 |