Literature DB >> 9880108

Diagnosis of bovine brucellosis using a homogeneous fluorescence polarization assay.

K Nielsen1, D Gall, M Lin, C Massangill, L Samartino, B Perez, M Coats, S Hennager, A Dajer, P Nicoletti, F Thomas.   

Abstract

To evaluate the fluorescence polarization assay (FPA) for the serological diagnosis of bovine brucellosis, 118 sera from cattle which were culture positive for Brucella abortus, 1751 sera from cattle from premises containing cattle infected with B. abortus, 1222 sera from cattle vaccinated with B. abortus strain 19 and 1199 sera from cattle with no evidence of brucellosis were tested in Argentina, Chile, Mexico and in the American states of Iowa, Missouri and Texas. Initial determination of serological positivity and negativity was based upon reactivity in currently used serological tests, consisting of a rapid screening test, the rose-bengal or the buffered plate antigen tests, followed by a second serological test, the complement fixation test. Sensitivity of the FPA (sera from culture positive animals) ranged from 87.5% to 100%. Serological positivity of cattle from infected premises ranged from 65.5% to 99.0% while the % negative cattle in herds without evidence of brucellosis was between 94.9 and 100%. Of B. abortus strain 19 vaccinated cattle which were positive in at least one in-use serological tests, 88.2% were negative in the FPA. In contrast, previous Canadian studies, sensitivity values were 99.0% and 100% and the specificity in both cases was 100%. This discrepancy was probably due to the use of less well characterized sera in the current study.

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Year:  1998        PMID: 9880108     DOI: 10.1016/s0165-2427(98)00195-0

Source DB:  PubMed          Journal:  Vet Immunol Immunopathol        ISSN: 0165-2427            Impact factor:   2.046


  6 in total

1.  Deletions of structural glycoprotein E2 of classical swine fever virus strain alfort/187 resolve a linear epitope of monoclonal antibody WH303 and the minimal N-terminal domain essential for binding immunoglobulin G antibodies of a pig hyperimmune serum.

Authors:  M Lin; F Lin; M Mallory; A Clavijo
Journal:  J Virol       Date:  2000-12       Impact factor: 5.103

2.  Effectiveness of Rose Bengal test and fluorescence polarization assay in the diagnosis of Brucella spp. infections in free range cattle reared in endemic areas in Zambia.

Authors:  J B Muma; A Lund; K Nielsen; G Matope; M Munyeme; K Mwacalimba; E Skjerve
Journal:  Trop Anim Health Prod       Date:  2008-10-28       Impact factor: 1.559

3.  Evaluation of primary binding assays for presumptive serodiagnosis of swine brucellosis in Argentina.

Authors:  P S Paulo; A M Vigliocco; R F Ramondino; D Marticorena; E Bissi; G Briones; C Gorchs; D Gall; K Nielsen
Journal:  Clin Diagn Lab Immunol       Date:  2000-09

4.  Evaluation of Brucella abortus phosphoglucomutase (pgm) mutant as a new live rough-phenotype vaccine.

Authors:  Juan Esteban Ugalde; Diego José Comerci; M Susana Leguizamón; Rodolfo Augusto Ugalde
Journal:  Infect Immun       Date:  2003-11       Impact factor: 3.441

5.  Evaluation and comparison of fluorescence polarization assay with three of the currently used serological tests in diagnosis of human brucellosis.

Authors:  A Konstantinidis; A Minas; S Pournaras; A Kansouzidou; P Papastergiou; A Maniatis; N Stathakis; C Hadjichristodoulou
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2007-10       Impact factor: 3.267

6.  Development of an improved competitive ELISA based on a monoclonal antibody against lipopolysaccharide for the detection of bovine brucellosis.

Authors:  Xiaolei Wang; Yan Wang; Limei Ma; Ran Zhang; Yanyan De; Xiaowen Yang; Chuanqing Wang; Qingmin Wu
Journal:  BMC Vet Res       Date:  2015-05-21       Impact factor: 2.741

  6 in total

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