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Molecular Cloning and Sequencing of the Circumsporozoite Protein Gene from Plasmodium falciparum Strain FCC-1/HN and Expression of the Gene in Mycobacteria

机译:恶性疟原虫FCC-1 / HN菌株环子孢子蛋白基因的分子克隆与序列分析及在分枝杆菌中的表达

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摘要

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.
机译:牛分枝杆菌Calmette-Guérin(BCG)已被用作一种活细菌疫苗,可以使超过20亿的人免疫结核病。为了将该疫苗株用作保护性抗原的载体,从恶性疟原虫基因组扩增了编码环孢子蛋白(CSP)的FCC-1 / HN株的恶性疟原虫基因,测序并在牛分枝杆菌BCG中表达在携带来自结核分枝杆菌的热休克蛋白70(HSP70)启动子的表达盒的控制下。通过电穿孔将重组穿梭质粒pBCG / CSP导入分枝杆菌,可以通过加热诱导携带pBCG / CSP的重组分枝杆菌表达CSP。重组CSP的分子量约为42 kDa。这份关于全长恶性疟原虫CSP基因在BCG中表达的报告为HSP70启动子在BCG中表达外源基因以及在BCG作为疟疾多价载体疫苗的开发中的应用提供了科学依据。

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