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Construction of an Expression Plasmid (Vector) Encoding Brucella Melitensis Outer Membrane Protein, a Candidate for DNA Vaccine

机译:编码布鲁氏菌外膜蛋白(DNA疫苗候选)的表达质粒(载体)的构建

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Background: DNA vaccination with plasmid encoding bacterial, viral, and parasitic immunogens has been shown to be an attractive method to induce efficient immune responses. Bacteria of the genus Brucella are facultative intracellular pathogens for which new and efficient vaccines are needed. Methods: To evaluate the use of a DNA immunization strategy for protection against brucellosis, a plasmid containing the DNA encoding the Brucella melitensis (B. melitensis) 31 kDa outer membrane protein, as a potent immunogenic target, was constructed. Results: The constructed plasmid, pcDNA3.1+omp31, was injected intramuscularly into mice and the expression of omp31 RNA was assessed by RT-PCR. The integrity of the pcDNA3.1+omp31 construct was confirmed with restriction analysis and sequencing. Omp31 mRNA expression was verified by RT-PCR. Conclusion: Our results indicate that the pcDNA3.1+omp31 eukaryotic expression vector expresses omp31 mRNA and could be useful as a vaccine candidate.
机译:背景:用编码细菌,病毒和寄生虫免疫原的质粒进行的DNA疫苗接种已被证明是诱导有效免疫应答的一种有吸引力的方法。布鲁氏菌属细菌是兼性的细胞内病原体,需要新的有效疫苗。方法:为了评估DNA免疫策略在预防布鲁氏菌病中的用途,构建了一个质粒,该质粒含有编码布鲁氏菌(B. melitensis)31 kDa外膜蛋白的DNA,作为有效的免疫原性靶标。结果:将构建的质粒pcDNA3.1 + omp31肌肉注射入小鼠体内,RT-PCR检测omp31 RNA的表达。通过限制性酶切分析和测序证实了pcDNA3.1 + omp31构建体的完整性。通过RT-PCR验证Omp31 mRNA的表达。结论:我们的结果表明,pcDNA3.1 + omp31真核表达载体可表达omp31 mRNA,可作为候选疫苗。

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