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作 者:付思美[1,2] 白耀霞[1] 曲勍[1,2] 徐杰[1] 王玉飞[1] 钟志军[1] 于爽[1] 王同坤[1] 杨毅[1] 陈燕芬[1,2] 汪舟佳[1] 杜昕颖[1] 黄留玉[1] 甄清[2] 陈泽良[1]
机构地区:[1]军事医学科学院疾病预防控制所,北京100071 [2]吉林大学公共卫生学院人畜共患病教育部重点实验室,吉林长春130021
出 处:《微生物学通报》2010年第8期1188-1193,共6页Microbiology China
基 金:国家863计划项目(No.2007AA02Z412);国家传染病重大专项项目(No.2008ZX10004-015;2009ZX10004-103)
摘 要:为分析vjbR在布鲁氏菌毒力中的作用,构建了vjbR的突变株和互补株,并分析了它们在巨噬细胞和小鼠体内的存活能力。利用同源重组的方法,用卡那抗性基因替换了16M的vjbR(BMEII1116)基因,得到了vjbR的缺失突变株16M△vjbR。将vjbR基因的ORF克隆到pMD18-T载体中,然后将其转入到突变株16M△vjbR中得到互补株16M△vjbR-C。用16M、16M△vjbR和16M△vjbR-C侵染巨噬细胞和感染小鼠,比较分析它们在巨噬细胞内的生存能力及小鼠毒力。研究结果表明vjbR突变株在巨噬细胞和小鼠体内的毒力减弱,存活能力下降,说明vjbR基因是布鲁氏菌16M的毒力相关基因,对于布鲁氏菌建立慢性感染是必要的。To evaluate the virulence roles of vjbR,the mutant and complementary strains of vjbR were constructed,and their survival capabilities in macrophage and mice were assayed.By using homologous recombination,the vjbR(BMEII1116) was replaced by kanamycin gene,resulting the deletion mutant 16M△vjbR.The ORF was PCR amplified and cloned into pMD-18T,which was transformed into mutant strain to generate the complementary strain 16M△vjbR-C.The three strains,16M,16M△vjbR and 16M△vjbR-C,were used to infect macrophage and mice,and their survival capability were assayed andcompared.The vjbR mutant strain16M△vjbR showed reduced survival in macrophage and mice,indicating that vjbR is a virulence gene of Brucella,and is essential for establishment of choronic infection.
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