Evaluation of Recombinant 28 kDa Outer Membrane Protein of Brucella abortus for the Clinical Diagnosis of Bovine Brucellosis in Korea

被引:32
|
作者
Lim, Jeong Ju [1 ]
Kim, Dong Hyeok [1 ]
Lee, Jin Ju [1 ]
Kim, Dae Geun [1 ]
Min, Wongi [1 ]
Lee, Hu Jang [1 ]
Rhee, Man Hee [2 ]
Chang, Hong Hee [3 ]
Kim, Suk [1 ,3 ]
机构
[1] Gyeongsang Natl Univ, Coll Vet Med, Jinju 660701, South Korea
[2] Kyungpook Natl Univ, Coll Vet Med, Taegu 702701, South Korea
[3] Gyeongsang Natl Univ, Inst Agr & Life Sci, Jinju 660701, South Korea
来源
JOURNAL OF VETERINARY MEDICAL SCIENCE | 2012年 / 74卷 / 06期
基金
新加坡国家研究基金会;
关键词
Brucella abortus; recombinant Omp28; serodiagnosis; LINKED-IMMUNOSORBENT-ASSAY; INTRACELLULAR GROWTH; MELITENSIS; ANTIGENS; RESPONSES; CLONING; CELLS; SHEEP; LIPOPOLYSACCHARIDE; EXPRESSION;
D O I
10.1292/jvms.11-0512
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Brucella spp. are Gram-negative, facultative, intracellular coccobacilli that are pathogenic to a variety of mammals, including ruminants and humans. The conventional serological test for diagnosing brucellosis in cattle in Korea is the standard tube agglutination test. However, agglutination tests sometimes give false-positive results due to cross-reactions with other pathogens. The outer membrane proteins of Brucella species have been extensively studied for their immunogenicity and serodiagnostic applications. However, an application of B. abortus OMPs for serodiagnosis has not been successfully established. In this study, cloning and expression of B. abortus Omp28, a group 3 antigen, were accomplished by PCR amplification cloning into a pMAL expression system, and purification of a recombinant Omp28 (rOmp28). The immunogenicity of rOmp28 was confirmed by Western blot analysis with Brucella-positive bovine serum. To determine whether rOmp2 has a potential benefit for use in the serodiagnosis of bovine brucellosis, rOmp28-based ELISA and latex bead agglutination test were performed. B. abortus positive (n=122) or negative (n=88) from TAT were positive (118/122, 96.7%) or negative (84/88, 95.4%) in ELISA and were positive (94/122, 77%) or negative (71/88, 81.7%) in that the latex bead agglutination test, respectively. The sensitivity, specificity and accuracy were 96.7, 95.4, 96.2% in ELISA and 77, 80.6, 78.5% in latex bead agglutination test, respectively. These findings suggest that the rOmp28 of B. abortus might be a good candidate for developing serological diagnostic tools for bovine brucellosis.
引用
收藏
页码:687 / 691
页数:5
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