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Expression of ORF2 partial gene of hepatitis E virus in tomatoes and immunoactivity of expression products

机译:戊型肝炎病毒戊型肝炎病毒ORF2部分基因在番茄中的表达及表达产物的免疫活性

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摘要

AIM: To transfer hepatitis E virus (HEV) ORF2 partial gene to tomato plants, to investigate its expression in transformants and the immunoactivity of expression products, and to explore the feasibility of developing a new type of plant-derived HEV oral vaccine.METHODS: Plant binary expression vector p1301E2, carrying a fragment of HEV open reading frame-2 (named HEV-E2), was constructed by linking the fragment to a constitutive CaMV35s promoter and nos terminator, then directly introduced into Agrobacterium tumefaciens EHA105. With leaf-disc method, tomato plants medicated by EHA105 were transformed and hygromycin-resistant plantlets were obtained in selective medium containing hygromycin. The presence and integration of foreign DNA in transgenic tomato genome were confirmed by Gus gene expression, PCR amplification and Southern dot blotting. The immunoactivity of recombinant protein extracted from transformed plants was examined by enzyme-linked immunosorbant assay (ELISA) using a monoclonal antibody specifically against HEV. ELISA was also used to estimate the recombinant protein content in leaves and fruits of the transformants.RESULTS: Seven positive lines of HEV-E2-transgenic tomato plants confirmed by PCR and Southern blotting were obtained and the immunoactivity of recombinant protein could be detected in extracts of transformants. The expression levels of recombinant protein were 61.22 ng/g fresh weight in fruits and 6.37-47.9 ng/g fresh weight in leaves of the transformants.CONCLUSION: HEV-E2 gene was correctly expressed in transgenic tomatoes and the recombinant antigen derived from them has normal immunoactivity. Transgenic tomatoes may hold a good promise for producing a new type of low-cost oral vaccine for hepatitis E virus.
机译:目的:将戊型肝炎病毒(ORV2)的部分基因转移到番茄植物中,研究其在转化体中的表达以及表达产物的免疫活性,并探讨开发新型植物源性HEV口服疫苗的可行性。通过将片段连接到组成型CaMV35s启动子和nos终止子上,构建携带HEV开放阅读框2片段(称为HEV-E2)的植物二元表达载体p1301E2,然后将其直接引入根癌农杆菌EHA105中。采用叶圆盘法,将含有EHA105的番茄植株转化,在含有潮霉素的选择性培养基中获得了对潮霉素具有抗性的苗。通过Gus基因表达,PCR扩增和Southern点杂交证实了外源DNA在转基因番茄基因组中的存在和整合。使用特异性针对HEV的单克隆抗体,通过酶联免疫吸附法(ELISA)检查了从转化植物中提取的重组蛋白的免疫活性。结果:通过PCR和Southern blotting鉴定获得7株HEV-E2转基因番茄植株的阳性蛋白,并在提取物中检测到重组蛋白的免疫活性。转化子。结果表明,HEV-E2基因在转基因番茄中正确表达,其衍生的重组抗原具有良好的表达能力。重组蛋白在果实中的表达量为61.22 ng / g鲜重,在叶片中为6.37-47.9 ng / g鲜重。正常的免疫活性。转基因番茄有望为生产新型的戊型肝炎病毒低成本口服疫苗提供良好的前景。

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