Singh Ankit, Srivastava Subhi, Chouksey Ankita, Panwar Bhupendra Singh, Verma Praveen C, Roy Sribash, Singh Pradhyumna K, Saxena Gauri, Tuli Rakesh
Plant Molecular Biology & Genetic Engineering, National Botanical Research Institute, Council of Scientific and Industrial Research, Rana Pratap Marg, Lucknow, 226001, UP, India.
Mol Biotechnol. 2015 Apr;57(4):359-70. doi: 10.1007/s12033-014-9829-y.
Transgenic hairy roots of Solanum lycopersicum were engineered to express a recombinant protein containing a fusion of rabies glycoprotein and ricin toxin B chain (rgp-rtxB) antigen under the control of constitutive CaMV35S promoter. Asialofetuin-mediated direct ELISA of transgenic hairy root extracts was performed using polyclonal anti-rabies antibodies (Ab1) and epitope-specific peptidal anti-RGP (Ab2) antibodies which confirmed the expression of functionally viable RGP-RTB fusion protein. Direct ELISA based on asialofetuin-binding activity was used to screen crude protein extracts from five transgenic hairy root lines. Expressions of RGP-RTB fusion protein in different tomato hairy root lines varied between 1.4 and 8 µg in per gram of tissue. Immunoblotting assay of RGP-RTB fusion protein from these lines showed a protein band on monomeric size of ~84 kDa after denaturation. Tomato hairy root line H03 showed highest level of RGP-RTB protein expression (1.14 %) and was used further in bench-top bioreactor for the optimization of scale-up process to produce large quantity of recombinant protein. Partially purified RGP-RTB fusion protein was able to induce the immune response in BALB/c mice after intra-mucosal immunization. In the present investigation, we have not only successfully scaled up the hairy root culture but also established the utility of this system to produce vaccine antigen which subsequently will reduce the total production cost for implementing rabies vaccination programs in developing nations. This study in a way aims to provide consolidated base for low-cost preparation of improved oral vaccine against rabies.
对番茄的转基因毛状根进行工程改造,使其在组成型CaMV35S启动子的控制下表达一种重组蛋白,该重组蛋白包含狂犬病糖蛋白和蓖麻毒素B链(rgp-rtxB)抗原的融合体。使用多克隆抗狂犬病抗体(Ab1)和表位特异性肽抗RGP(Ab2)抗体对转基因毛状根提取物进行去唾液酸胎球蛋白介导的直接ELISA,证实了功能上可行的RGP-RTB融合蛋白的表达。基于去唾液酸胎球蛋白结合活性的直接ELISA用于筛选来自五个转基因毛状根系的粗蛋白提取物。不同番茄毛状根系中RGP-RTB融合蛋白的表达量在每克组织1.4至8微克之间。对这些品系的RGP-RTB融合蛋白进行免疫印迹分析,结果显示变性后单体大小约为84 kDa处有一条蛋白带。番茄毛状根系H03显示出最高水平的RGP-RTB蛋白表达(1.14%),并进一步用于台式生物反应器中,以优化放大过程,从而大量生产重组蛋白。部分纯化的RGP-RTB融合蛋白在黏膜内免疫后能够诱导BALB/c小鼠产生免疫反应。在本研究中,我们不仅成功扩大了毛状根培养规模,还确立了该系统生产疫苗抗原的实用性,这随后将降低发展中国家实施狂犬病疫苗接种计划的总生产成本。本研究旨在为低成本制备改良狂犬病口服疫苗提供坚实基础。