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Serological crossreactivity between Brucella abortus and Yersinia enterocolitica 0:9 III. Specificity of the in vitro antigen-specific gamma interferon test for bovine brucellosis diagnosis in experimentally Yersinia enterocolitica 0:9-infected cattle
Institution:1. Department of Endocrinology, 424 General Military Hospital, Thessaloniki, Greece;2. Laboratory for the Research of Musculoskeletal System “Th. Garofalidis,” Medical School, National and Kapodistrian University of Athens, KAT Hospital, Greece;3. Department of Computed Tomography, Asklepeion Voulas Hospital, Athens, Greece;4. First Laboratory of Pharmacology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece;5. Department of Endocrinology and Diabetes and Department of Medical Research, 251 Hellenic Airforce and VA Hospital, Athens, Greece;1. Faculty of Medicine, Tokat Gaziosmanpasa University, Department of Medical Biology, Tokat, Turkey;2. Department of Infectious Diseases and Clinical Microbiology, Saglik Bilimleri University, Dr. Abdurrahman Yurtaslan Ankara Oncology Training & Research Hospital, Ankara, Turkey;3. Faculty of Medicine, Tokat Gaziosmanpasa University, Department of Infectious Diseases and Clinical Microbiology, Tokat, Turkey;4. Faculty of Medicine, Tokat Gaziosmanpasa University, Department of Emergency Medicine, Tokat, Turkey
Abstract:The course of immunological reaction in 10 Yersinia enterocolitica 0:9 experimentally-infected heifers was followed using the conventional brucellosis tests complement fixation test (CFT), serum agglutination test (SAT) and brucella card test (BCT), and a recently developed Brucella antigen-specific gamma interferon (IFN-γ) test. Initially, the animals were exposed orally to 1010 colony-forming units (CFU) of Y. enterocolitica 0:9. Four weeks later, they were inoculated intravenously with 108 CFU of Y. enterocolitica 0:9 cells. After oral inoculation, the response in the conventional brucellosis tests was minimal. Only after intravenous inoculation were CFT and SAT titres and BCT reactions comparable to natural, false positive brucellosis reactors. After oral exposure the Brucellergen-stimulated release of IFN-γ peaked at values above the cut-off stimulation index of 2.5 in 80% of the heifers. After intravenous inoculation, stimulation indices above 2.5 were present in only 10% of the animals. Two B. abortus infected control cattle showed stimulation indices of 3.1 and 3.4, and a negative control animal exhibited a stimulation index of 1.0. These findings show, in contrast to a previous study, that the Brucellergen-specific IFN-γ assay cannot be used as a specific and discriminatory test for B. abortus infections.
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