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布鲁氏菌pcDNA3.1-omp17.3基因疫苗的研制
引用本文:邓小红,曾政,王希良.布鲁氏菌pcDNA3.1-omp17.3基因疫苗的研制[J].中国兽医科技,2007,37(6):505-509.
作者姓名:邓小红  曾政  王希良
作者单位:[1]重庆工商大学药物化学与化学生物学研究中心,重庆400067 [2]重庆市动物疫病预防控制中心,重庆401147 [3]军事医学科学院微生物流行病研究所,北京100071
基金项目:国家自然科学基金项目(30170853)
摘    要:采用PCR方法扩增了布鲁氏菌17.3ku外膜蛋白编码基因,并将该基因克隆至真核表达载体pcDNA3.1(+)中,成功构建了真核表达质粒pcDNA3.1-ompl7.3。pcDNA3.1-omp17.3转染coS-7细胞后,通过Western—blotting检测到了17.3ku蛋白的瞬时表达。将pcDNA3.1-ompl7.3免疫小鼠,三免后经ELISA、流式细胞仪以及ELISPOT技术检测到pcDNA3.1-omp17.3在小鼠体内诱导产生了以Th1型为主的细胞免疫应答。结果表明,构建的基因疫苗可作为潜在的布鲁氏菌新型疫苗,有进一步研究的意义。

关 键 词:布鲁氏菌  17.3  ku蛋白  基因疫苗  免疫应答
文章编号:1673-4696(2007)06-0505-05
收稿时间:2007-01-15
修稿时间:2007-05-17

Development of DNA vaccine pcDNA3.1-omp17.3 against Brucella
DENG Xiao-hong , ZENG Zheng , WANG Xi-liang.Development of DNA vaccine pcDNA3.1-omp17.3 against Brucella[J].Chinese Journal of Veterinary Science and Technology,2007,37(6):505-509.
Authors:DENG Xiao-hong  ZENG Zheng  WANG Xi-liang
Abstract:The ompl7.3 gene of Brucella abortus was amplified by PCR and then the amplicon was cloned into the eukaryotic expression plasmid pcDNA3.1 to construct a recombinant plasmid pcDNA3. 1- omplT. 3. Then the recombinant plasmid pcDNA3. 1-omplT. 3 was transfected into COS7 cells, and the expressed OMP 17. 3 was detected by Western-blotting. The recombinant plasmid was injected into BALB/c mice intramuscularly. The immunized mice were induced to produce a typical T helper 1 dominated immune response, as determined by ELISA, Flow Cytometer and ELISPOT method. The results Showed that pcDNA3.1-omp17. 3 was a potential candidate vaccine for the controlling of brucellosis.
Keywords:Brucella  17  3 ku protein  gene vaccine  immune response
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