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1 March 2003 Molecular Cloning and Sequencing of the Merozoite Surface Antigen 2 Gene from Plasmodium falciparum Strain FCC-1/HN and Expression of the Gene in Mycobacteria
CHUNFU ZHENG, PEIMEI XIE, YATANG CHEN
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Abstract

Strain bacillus Calmette-Guerin (BCG) of Mycobacterium bovis has been used as a live bacterial vaccine to immunize more than 3 billion people against tuberculosis. In an attempt to use this vaccine strain as a vehicle for protective antigens, the gene encoding merozoite surface antigen 2 (MSA2) was amplified from strain FCC-1/HN Plasmodium 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/MSA2 was introduced into mycobacteria by electroporation, and the recombinant mycobacteria harboring pBCG/MSA2 could be induced by heating to express MSA2; the molecular mass of recombinant MSA2 was about 31 kDa. This first report of expression of the full-length P. falciparum MSA2 gene in BCG provides evidence for use of the HSP70 promoter in expressing a foreign gene in BCG and in development of BCG as a multivalent vectoral vaccine for malaria.

CHUNFU ZHENG, PEIMEI XIE, and YATANG CHEN "Molecular Cloning and Sequencing of the Merozoite Surface Antigen 2 Gene from Plasmodium falciparum Strain FCC-1/HN and Expression of the Gene in Mycobacteria," The Journal of Eukaryotic Microbiology 50(2), 140-143, (1 March 2003). https://doi.org/10.1111/j.1550-7408.2003.tb00249.x
Received: 20 September 2002; Accepted: 27 January 2003; Published: 1 March 2003
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KEYWORDS
Electroporation
heat shock protein 70
malaria
Mycobacterium bovis
shuttle plasmid
strain bacillus Calmette-Guerin
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