Wu H, Singh N K, Locy R D, Scissum-Gunn K, Giambrone J J
Department of Poultry Science, Auburn University, AL 36849, USA.
Biotechnol Lett. 2004 May;26(10):787-92. doi: 10.1023/b:bile.0000025878.30350.d5.
VP2 protein is the major host-protective immunogen of infectious bursal disease virus (IBDV) of chickens. Transgenic lines of Arabidopsis thaliana expressing recombinant VP2 were developed. The VP2 gene of an IBDV antigenic variant E strain was isolated, amplified by RT-PCR and introduced into a plant expression vector, pE1857, having a strong promoter for plant expression. A resulting construct with a Bar gene cassette for bialaphos selection in plant (rpE-VP2) was introduced into Agrobacterium tumefaciens by electroporation. Agrobacterium containing the rpE-VP2 construct was used to transform Ar. thaliana and transgenic plants were selected using bialaphos. The presence of VP2 transgene in plants was confirmed by PCR and Southern blot analysis and its expression was confirmed by RT-PCR. Western blot analysis and antigen-capture ELISA assay using monoclonal anti-VP2 were used to determine the expression of VP2 protein in transgenic plants. The level of VP2 protein in the leaf extracts of selected transgenic plants varied from 0.5% to 4.8% of the total soluble protein. Recombinant VP2 protein produced in plants induced antibody response against IBDV in orally-fed chickens.
VP2蛋白是鸡传染性法氏囊病病毒(IBDV)主要的宿主保护性免疫原。构建了表达重组VP2的拟南芥转基因株系。分离出IBDV抗原变异E株的VP2基因,通过逆转录聚合酶链反应(RT-PCR)进行扩增,并将其导入具有用于植物表达的强启动子的植物表达载体pE1857中。通过电穿孔法将带有用于植物中双丙氨膦选择的Bar基因盒的构建体(rpE-VP2)导入根癌农杆菌。含有rpE-VP2构建体的农杆菌用于转化拟南芥,并使用双丙氨膦筛选转基因植物。通过PCR和Southern印迹分析证实植物中VP2转基因的存在,并通过RT-PCR证实其表达。使用抗VP2单克隆抗体的蛋白质印迹分析和抗原捕获ELISA测定法来确定转基因植物中VP2蛋白的表达。所选转基因植物叶片提取物中VP2蛋白的水平占总可溶性蛋白的0.5%至4.8%。植物中产生的重组VP2蛋白在口服给药的鸡中诱导了针对IBDV的抗体反应。