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作 者:彭小兵[1] 彭国瑞[1] 李旭妮[1] 董令赢 冯丽芳 蒋玉文[1] PENG Xiao-bing;PENG Guo-rui;LI Xu-ni;DONG Ling-ying;FENG Li-fang;JIANG Yu-wen(China Institute of Veterinary Drug Control,Beijing 100081,China;Beijing Zhonghai BiotechCo.,Ltd,Beijing 1000819 China)
机构地区:[1]中国兽医药品监察所,北京100081 [2]北京中海生物科技有限公司,北京100081
出 处:《中国兽医学报》2019年第8期1500-1505,共6页Chinese Journal of Veterinary Science
基 金:国家重点研发计划基金资助项目(2017YFD0500905)
摘 要:为了确定产气荚膜梭菌ε毒素(ETX)和α毒素(CPA)无毒突变体作为亚单位疫苗同时预防D型和A型产气荚膜梭菌病的免疫效果,试验用点突变结合OEPR法构建重组质粒pET32a-mETX-mCPA。将阳性重组质粒转入E.coli BL21(DE3)中,以预先添加乳糖的自诱导培养基表达目的蛋白。经SDS-PAGE分析,其表达的蛋白相对分子质量约为92 000,与预期值一致。Western blot检测结果表明,重组蛋白可被A型产气荚膜梭菌阳性血清所识别。致死性试验结果表明,重组蛋白不致死小鼠。以铝胶为佐剂将重组蛋白免疫家兔,二免血清0.1 mL可分别中和3个小鼠MLD的A型毒素和100个小鼠MLD的D型毒素。本研究用OEPR法成功构建了无毒突变体pET32a-mETX-mCPA质粒,获得的重组蛋白在家兔上显示出良好的免疫效果,为研发A、D型产气荚膜梭菌二价亚单位疫苗奠定理论基础。In order to determine the immune effect of the recombinant protein mETX-mCPA as a subunit vaccine for preventing diseases caused by Clostridium perfringens type D and A,the recombinant expression plasmid pET32 a-mETX-mCPA was constructed by OEPR(overlap extension PCR and recombination) and site-directed mutagenesis.The positive recombinant plasmid was transformed into E.coli BL21(DE3),and the target protein was expressed in the auto-inducing medium including lactose.The expression product was identified by SDS-PAGE and found to be 92 000 as expected and confirmed by Western blot with Clostriudm perfringens type A antisera.Recombinant protein could not make mice die.Upon immunization of rabbit twice using the recombinant protein with aluminium hydroxide gel,the second rabbit immune sera neutralization titers against Clostridium perfringens type A toxin and type D toxin were 3 and 100 respectively.The non-toxic mutant pET32 a-mETX-mCPA was successfully constructed by OEPR,the obtained recombinant protein showed a good immune effect,providing basic data for subsequent development of subunit vaccine.
关 键 词:ETX CPA 产气荚膜梭菌 OEPR法 免疫效果 家兔
分 类 号:S852.61[农业科学—基础兽医学] R535[农业科学—兽医学]
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