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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68894
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dc.contributor.authorGarcia, João Luis-
dc.contributor.authorNavarro, Italmar Teodorico-
dc.contributor.authorVidotto, Odilon-
dc.contributor.authorGennari, Solange Maria-
dc.contributor.authorMachado, Rosângela Zacarias-
dc.contributor.authorPereira, Ademir Benedito da Luz-
dc.contributor.authorSinhorini, Idercio Luiz-
dc.date.accessioned2014-05-27T11:21:52Z-
dc.date.accessioned2016-10-25T18:22:12Z-
dc.date.available2014-05-27T11:21:52Z-
dc.date.available2016-10-25T18:22:12Z-
dc.date.issued2006-06-01-
dc.identifierhttp://dx.doi.org/10.1016/j.exppara.2005.12.011-
dc.identifier.citationExperimental Parasitology, v. 113, n. 2, p. 100-105, 2006.-
dc.identifier.issn0014-4894-
dc.identifier.issn1090-2449-
dc.identifier.urihttp://hdl.handle.net/11449/68894-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68894-
dc.description.abstractIndirect ELISA and IFAT have been reported to be more sensitive and specific than agglutination tests. However, MAT is cheaper, easier than the others and does not need special equipment. The purpose of this study was to compare an enzyme linked immunosorbent assay using crude rhoptries of Toxoplasma gondii as coating wells (r-ELISA) with indirect fluorescence antibody test (IFAT) and modified agglutination test (MAT) to detect anti-T. gondii antibodies in sera of experimentally infected pigs. Ten mixed breed pigs between 6.5 and 7.5 weeks old were used. All pigs were negative for the presence of T. gondii antibodies by IFAT (titre < 16), r-ELISA (OD < 0.295) and MAT (titre < 16). Animals received 7 × 107 viable tachyzoites of the RH strain by intramuscular (IM) route at day 0. Serum samples were collected at days -6, 0, 7, 14, 21, 28, 35, 42, 50, and 57. IFAT detected anti-T. gondii antibodies earlier than r-ELISA and MAT. The average of antibody levels was higher at day 35 in IFAT (Log10 = 2.9) and in MAT (Log10 = 3.5), and at day 42 in r-ELISA (OD = 0.797). The antibody levels remained high through the 57th day after inoculation in MAT, and there was a decrease tendency in r-ELISA and IFAT. IFAT was used as gold standard and r-ELISA demonstrated a higher prevalence (73.3%), sensitivity (94.3%), negative predictive value (83.3%), and accuracy (95.6%) than MAT. Kappa agreements among tests were calculated, and the best results were shown by r-ELISA × IFAT (κ = 0.88, p < 0.001). Cross-reaction with Sarcocystis miescheriana was investigated in r-ELISA and OD mean was 0.163 ± 0.035 (n = 65). Additionally, none of the animals inoculated with Sarcocystis reacted positively in r-ELISA. Our results indicate that r-ELISA could be a good method for serological detection of T. gondii infection in pigs. © 2005 Elsevier Inc. All rights reserved.en
dc.format.extent100-105-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectApicomplexa-
dc.subjectELISA-
dc.subjectenzyme linked immunosorbent assay-
dc.subjectIFAT-
dc.subjectindirect fluorescence antibody test-
dc.subjectMAT-
dc.subjectmodified agglutination test-
dc.subjectPig-
dc.subjectRhoptry antigens-
dc.subjectToxoplasma gondii-
dc.subjectToxoplasmosis-
dc.subjectantibody-
dc.subjectdiagnostic agent-
dc.subjectimmunoglobulin G-
dc.subjectmembrane protein-
dc.subjectprotozoon antibody-
dc.subjectROP 1 protein, Toxoplasma gondii-
dc.subjectagglutination test-
dc.subjectanimal cell-
dc.subjectanimal experiment-
dc.subjectanimal tissue-
dc.subjectantibody blood level-
dc.subjectantibody detection-
dc.subjectantibody titer-
dc.subjectblood sampling-
dc.subjectcalculation-
dc.subjectcontrolled study-
dc.subjectcross reaction-
dc.subjectdiagnostic accuracy-
dc.subjectdiagnostic value-
dc.subjectfluorescent antibody technique-
dc.subjectinoculation-
dc.subjectintermethod comparison-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectSarcocystis-
dc.subjectserodiagnosis-
dc.subjectswine-
dc.subjectanimal-
dc.subjectanimal parasitosis-
dc.subjectbiosynthesis-
dc.subjectblood-
dc.subjectcomparative study-
dc.subjectfemale-
dc.subjectimmunology-
dc.subjectisolation and purification-
dc.subjectmale-
dc.subjectmethodology-
dc.subjectprediction and forecasting-
dc.subjectprevalence-
dc.subjectrandomization-
dc.subjectsensitivity and specificity-
dc.subjecttime-
dc.subjectToxoplasma-
dc.subjectAnimalia-
dc.subjectSarcocystis miescheriana-
dc.subjectSus scrofa-
dc.subjectAgglutination Tests-
dc.subjectAnimals-
dc.subjectAntibodies, Protozoan-
dc.subjectEnzyme-Linked Immunosorbent Assay-
dc.subjectFemale-
dc.subjectFluorescent Antibody Technique, Indirect-
dc.subjectImmunoglobulin G-
dc.subjectMale-
dc.subjectMembrane Proteins-
dc.subjectPredictive Value of Tests-
dc.subjectPrevalence-
dc.subjectRandom Allocation-
dc.subjectSensitivity and Specificity-
dc.subjectSwine-
dc.subjectTime Factors-
dc.subjectToxoplasmosis, Animal-
dc.titleToxoplasma gondii: Comparison of a rhoptry-ELISA with IFAT and MAT for antibody detection in sera of experimentally infected pigsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationMicrobiology and Immunology Laboratory Departamento de Biologia Universidade Estadual, R. Simeao Camargo Varela Sa, 03, Bairro Cascavel, Guarapuava, PR-
dc.description.affiliationProtozoology Laboratory Departamento de Medicina Veterinária Preventiva Universidade Estadual de Londrina-UEL, Postal Box 6001, 86050-970 Londrina, PR-
dc.description.affiliationParasitology Laboratory Departamento de Medicina Veterinária e Saúde Animal Universidade de São Paulo-USP, Av. Prof. Orlando Marques Paiva, 87, 05508-000 São Paulo, SP-
dc.description.affiliationImmunoparasitology Laboratory Departamento de Patologia Veterinária Universidade Estadual de São Paulo-UNESP, Via Acesso P Donato Castellane Km 5, 14884-9000 Jaboticabal, SP-
dc.description.affiliationElectronic Microscopy Laboratory Departamento de Patologia FMVZ-USP, Av. Prof. Orlando Marques Paiva, 87, 05508-000 São Paulo, SP-
dc.description.affiliationUnespImmunoparasitology Laboratory Departamento de Patologia Veterinária Universidade Estadual de São Paulo-UNESP, Via Acesso P Donato Castellane Km 5, 14884-9000 Jaboticabal, SP-
dc.identifier.doi10.1016/j.exppara.2005.12.011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofExperimental Parasitology-
dc.identifier.scopus2-s2.0-33745151992-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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