Zheng C, Xie P, Chen Y
Institute of Infectious and Parasitic Diseases, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, People's Republic of China.
J Clin Microbiol. 2001 Aug;39(8):2911-5. doi: 10.1128/JCM.39.8.2911-2915.2001.
Mycobacterium bovis bacillus Calmette-Guérin (BCG) has been used as a live bacterial vaccine to immunize more than 2 billion people against tuberculosis. In an attempt to use this vaccine strain as a vehicle for protective antigens, the Plasmodium falciparum gene from strain FCC-1/HN encoding circumsporozoite protein (CSP) was amplified from the P. falciparum genome, sequenced, and expressed in M. bovis BCG under the control of an expression cassette carrying the promoter of heat shock protein 70 (HSP70) from Mycobacterium tuberculosis. The recombinant shuttle plasmid pBCG/CSP was introduced into mycobacteria by electroporation, and the recombinant mycobacteria harboring pBCG/CSP could be induced by heating to express CSP; the molecular mass of recombinant CSP was about 42 kDa. This report of expression of the almost-full-length P. falciparum CSP gene in BCG provides scientific evidence for the application of the HSP70 promoter in expressing a foreign gene in BCG and in development of BCG as a multivalent vectoral vaccine for malaria.
牛分枝杆菌卡介苗(BCG)已作为一种活细菌疫苗用于免疫超过20亿人以预防结核病。为了将这种疫苗菌株用作保护性抗原的载体,从恶性疟原虫基因组中扩增、测序了编码环子孢子蛋白(CSP)的FCC-1/HN株恶性疟原虫基因,并在携带结核分枝杆菌热休克蛋白70(HSP70)启动子的表达盒控制下在牛分枝杆菌卡介苗中表达。通过电穿孔将重组穿梭质粒pBCG/CSP导入分枝杆菌,携带pBCG/CSP的重组分枝杆菌可通过加热诱导表达CSP;重组CSP的分子量约为42 kDa。该关于在卡介苗中表达几乎全长恶性疟原虫CSP基因的报告为HSP70启动子在卡介苗中表达外源基因以及将卡介苗开发为疟疾多价载体疫苗的应用提供了科学依据。