摘要
目的 :构建表达幽门螺杆菌 (H pylori)hpaA的重组减毒鼠伤寒沙门氏疫苗菌。方法 :用基因工程的方法将hpaA基因克隆入原核表达质粒pTrc99A ,并进行了基因测序。重组质粒经鉴定后再导入减毒鼠伤寒沙门氏菌SL32 6 1,提取重组疫苗菌质粒 ,PCR和酶切鉴定 ,筛选阳性克隆。用SDS PAGE电泳和Westernblot进行HpaA表达和鉴定。结果 :经PCR和酶切证实 ,构建了含hpaA的重组原核表达质粒pTrc99A hpaA ,并将后者成功转化了减毒鼠伤寒沙门氏菌。HpaA能在疫苗菌中以二聚体形式表达 ,HpaA量约占全菌体蛋白量的 17% ,Westernblot证实其有免疫原性。结论 :构建了表达H pylorihpaA的重组减毒鼠伤寒沙门氏疫苗菌 ,为探索制备H
Objective:To construct a recombinant live attenuated Salmonella typhimurium vaccine strain expressing Helicobacter pylori hpaA gene.Methods:By genetic engineering methods,hpaA gene was cloned into a procaryotic expression plasmid pTrc99A,and the identified recombinant plasmid was then used to transform an attenuated Salmonella typhimurium vaccine strain SL3261,and the positive clones were screened by PCR and restriction enzyme digestion. HpaA expression was analyzed by SDS PAGE and Western blot.Results:Confirmed by PCR and restriction enzyme digestion ,a recombinant procaryotic expression plasmid pTrc99A hpaA was constructed,and then introduced into an attenuated Salmonella typhimurium vaccine strain SL3261 successfully. HpaA was expressed in the recombinant strains in the form of a dimer,and also its immunogenicity was confirmed by Western blot. Conclusion:A recombinant live attenuated Salmonella typhimurium vaccine strain expressing Helicobacter pylori hpaA gene was constructed and identified,and this work will help to develop an oral recombinant live vaccine against Helicobacter pylori.
出处
《中国免疫学杂志》
CAS
CSCD
北大核心
2001年第3期148-151,共4页
Chinese Journal of Immunology
基金
卫生部临床学科重点项目! (No .970 40 2 2 6 )
广东省科技计划重点攻关项目! (No .99No.480 2G)
广东省自然科学基金课题!(No 990 0