Fatemeh Ghaffarifar, Fatemeh Tabatabaie, Zohreh Sharifi, Abdolhosein Dalimiasl, Mohammad Zahir Hassan, Mehdi Mahdavi
Department of Parasitology, Faculty of Medical Sciences, Tarbiat Modares University, PO Box 14115-111, Tehran, Iran.
Malays J Med Sci. 2012 Jan;19(1):15-9.
TSA (thiol-specific antioxidant antigen) is the immune-dominant antigen of Leishmania major and is considered to be the most promising candidate molecule for a recombinant or DNA vaccine against leishmaniasis. The aim of the present work was to express a plasmid containing the TSA gene in eukaryotic cells.
Genomic DNA was extracted, and the TSA gene was amplified by polymerase chain reaction (PCR). The PCR product was cloned into the pTZ57R/T vector, followed by subcloning into the eukaryotic expression vector pcDNA3 (EcoRI and HindIII sites). The recombinant plasmid was characterised by restriction digest and PCR. Eukaryotic Chinese hamster ovary cells were transfected with the plasmid containing the TSA gene. Expression of the L. major TSA gene was confirmed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis and Western blotting.
The plasmid containing the TSA gene was successfully expressed, as demonstrated by a band of 22.1 kDa on Western blots.
The plasmid containing the TSA gene can be expressed in a eukaryotic cell line. Thus, the recombinant plasmid may potentially be used as a DNA vaccine in animal models.
硫醇特异性抗氧化剂抗原(TSA)是硕大利什曼原虫的免疫显性抗原,被认为是抗利什曼病重组疫苗或DNA疫苗最有前景的候选分子。本研究的目的是在真核细胞中表达含TSA基因的质粒。
提取基因组DNA,通过聚合酶链反应(PCR)扩增TSA基因。将PCR产物克隆到pTZ57R/T载体中,随后亚克隆到真核表达载体pcDNA3(EcoRI和HindIII位点)。通过限制性酶切和PCR对重组质粒进行鉴定。用含TSA基因的质粒转染真核中国仓鼠卵巢细胞。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质印迹法确认硕大利什曼原虫TSA基因的表达。
蛋白质印迹显示出现一条22.1 kDa的条带,证明含TSA基因的质粒成功表达。
含TSA基因的质粒可在真核细胞系中表达。因此,该重组质粒有可能在动物模型中用作DNA疫苗。