Comparative evaluation of recombinant BP26 protein for serological diagnosis of Brucella melitensis infection in goats

被引:14
作者
Gupta, V. K. [1 ]
Kumari, Ranjeeta [1 ]
Vohra, Jyoti [1 ]
Singh, S. V. [1 ]
Vihan, V. S. [1 ]
机构
[1] Cent Inst Res Goats, Microbiol Lab, Div Anim Hlth, Mathura 281122, Uttar Pradesh, India
关键词
Brucella melitensis; Recombinant BP26; ELISA; SAT; CFT; PCR goats; LINKED-IMMUNOSORBENT-ASSAY; POLYMERASE-CHAIN-REACTION; SINGLE-STEP PCR; BOVINE BRUCELLOSIS; MONOCLONAL-ANTIBODIES; CYTOSOLUBLE PROTEINS; IMMUNODIFFUSION TEST; CAPRINE-BRUCELLOSIS; COMPETITIVE ELISA; VACCINATED SHEEP;
D O I
10.1016/j.smallrumres.2010.05.009
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
An enzyme-linked immunosorbent assay (ELISA) was developed for the serological diagnosis of caprine brucellosis with purified recombinant BP26 (outer membrane protein 28) of Brucella melitensis 16M produced in Escherichia coli. Brucella protein named CP28, BP26, or Omp28 has been identified as an immunodominant antigen in infected cattle, sheep, goats, and humans. The recombinant BP26(rBP6) ELISA performed with serum samples (n = 1738) taken from organized farms and field goats from Northern India and tested in two different batches of 778 and 960 animals for brucellosis. Positive results were compared with the traditional serum agglutination test (SAT), complement fixation test (CFT) and dot-ELISA. The diagnostic sensitivity of rBP26 ELISA, SAT, CFT and dot-ELISA was 87.5%, 56.25%, 62.5% and 75% respectively. The specificity of the rBP26 ELISA, SAT, CFT and clot-ELISA was 90%, 75%, 80%, and 85% respectively. The results of rBP26 ELISA positive animals were further compared and evaluated by tissue PCR using B. melitensis BP26 gene as target. This resulted in 100% positive correlation between rBP26 ELISA and BP26 PCR. Thus, these results confirmed the importance of BP26 as a suitable antigen and rBP26 ELISA, if well standardized, proved to be a good screening test for the serological diagnosis of caprine brucellosis. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 125
页数:7
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