基于bacmid的香蕉束顶病毒外壳蛋白基因在昆虫细胞中的表达重组杆状病毒的生成

W. Elmenofy, I. Ismail, H. N. El-Din
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摘要

香蕉束顶病是由香蕉束顶病毒(BBTV)引起的最具破坏性的病毒性疾病之一。使用病毒颗粒作为抗原,通过普通血清学技术生产多克隆和单克隆抗体,在病毒颗粒的纯度和浓度以及由此产生的抗体方面存在一些缺点。在多角蛋白启动子(Polyhedrin promoter, Polh)的控制下,利用杆状病毒表达载体系统(BEVS)表达了BBTV的外壳蛋白基因(CP)。由此,生成了由CP基因和改良的绿色荧光蛋白(GFP)基因组成的卡带。重组病毒(vAc-CPpolh-GFPp10)经PCR分析证实。倒置荧光显微镜下,利用GFP蛋白荧光成功检测了重组病毒在Sf9昆虫细胞中的传播。将生成的重组病毒在Sf9细胞中扩增,用感染细胞的裂解液Dot blot检测CP的表达。抗BBTV多克隆抗体与表达于Sf9细胞和BBTV侵染植株的重组CP有血清学反应。该结果提示利用BBTV表达的CP进一步开发抗血清的可能性,该抗血清可用于检测被侵染植物的BBTV。
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GENERATION OF BACMID-BASED RECOMBINANT BACULOVIRUS FOR BANANA BUNCHY TOP VIRUS COAT PRO-TEIN GENE EXPRESSION IN INSECT CELLS
Bunchy top disease is one of the most destructive viral diseases caused by the Banana Bunchy Top Virus (BBTV). Using of virus particles as an antigen for polyclonal and monoclonal antibodies production by common serological techniques has several disadvantages concerning the purity and concentration of the viral particles and by extension the produced antibodies. In this study, the coat protein gene (CP) of BBTV was expressed using baculovirus expression vector system (BEVS) under the control of the Polyhedrin promoter (Polh). Accordingly, the generated cassette consisting of the CP gene and the improved Green Florescent Protein (GFP) gene. The generated recombinant virus (vAc-CPpolh-GFPp10) was proved using PCR analysis. Spreading of the recombinant virus in Sf9 insect cells was successfully detected using GFP protein florescence under inverted fluorescent microscopy. The generated recombinant virus was amplified in Sf9 cells and the expression of CP was tested using the infected cell lysate by Dot blot analysis. The anti-BBTV polyclonal antibodies serologically reacted with the recombinant CP which was expressed in Sf9 cells as well as to the BBTV infected plants. This result suggested the possibility of using the expressed CP of BBTV for further development of antisera that can be implemented for BBTV detection in infected plants.
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