Biemelt Sophia, Sonnewald Uwe, Galmbacher Petra, Willmitzer Lothar, Müller Martin
Institut für Pflanzengenetik und Kulturpflanzenforschung, 06466 Gatersleben, Germany.
J Virol. 2003 Sep;77(17):9211-20. doi: 10.1128/jvi.77.17.9211-9220.2003.
Cervical cancer is linked to infection with human papillomaviruses (HPV) and is the third most common cancer among women worldwide. There is a strong demand for the development of an HPV preventive vaccine. Transgenic plants expressing the HPV major capsid protein L1 could be a system to produce virus-like particles for prophylactic vaccination or could even be used as edible vaccines to induce an L1-specific prophylactic immune response. Here, we describe the generation of transgenic tobacco and potato plants carrying the HPV type 16 major structural gene L1 under the control of the cauliflower mosaic virus 35S promoter. All attempts to express either the original, unmodified L1 gene or an L1 gene with a codon usage optimized for expression in plants failed. Surprisingly, small amounts of the protein were detected using an L1 gene optimized for expression in human cells. However, Northern blot analysis revealed that most of the L1 transcripts were degraded. Introduction of the translational enhancer Omega derived from the tobacco mosaic virus strongly increased transcript stability and resulted in accumulation of L1 protein to approximately 0.5 to 0.2% of total soluble protein in transgenic tobacco and potato plants, respectively. The plant-derived L1 protein displayed conformation-specific epitopes and assembled into virus-like particles. Furthermore, we did not find any indications of protein modification of the L1 protein produced in plants. Plant-derived L1 was as immunogenic as L1 expressed in baculovirus-infected insect cells. Feeding of tubers from transgenic potatoes to mice induced an anti-L1 antibody response in 3 out of 24 mice, although this response was only transient in two of the mice. Our data, however, indicate that an anti-L1 response was primed in about half of the 24 animals.
宫颈癌与人乳头瘤病毒(HPV)感染有关,是全球女性中第三大常见癌症。对开发HPV预防性疫苗有强烈需求。表达HPV主要衣壳蛋白L1的转基因植物可能是一种生产用于预防性疫苗接种的病毒样颗粒的系统,甚至可作为可食用疫苗用于诱导L1特异性预防性免疫反应。在此,我们描述了在花椰菜花叶病毒35S启动子控制下携带HPV 16型主要结构基因L1的转基因烟草和马铃薯植株的产生。表达原始的、未修饰的L1基因或经密码子优化以在植物中表达的L1基因的所有尝试均失败。令人惊讶的是,使用在人类细胞中优化表达的L1基因检测到了少量蛋白质。然而,Northern印迹分析表明大多数L1转录本被降解。引入源自烟草花叶病毒的翻译增强子Omega极大地提高了转录本稳定性,并导致转基因烟草和马铃薯植株中L1蛋白分别积累至总可溶性蛋白的约0.5%至0.2%。植物来源的L1蛋白显示出构象特异性表位并组装成病毒样颗粒。此外,我们未发现植物中产生的L1蛋白有任何蛋白质修饰的迹象。植物来源的L1与在杆状病毒感染的昆虫细胞中表达的L1一样具有免疫原性。将转基因马铃薯块茎喂给小鼠,24只小鼠中有3只诱导出抗L1抗体反应,不过其中两只小鼠中的这种反应只是短暂的。然而,我们的数据表明,在24只动物中约有一半启动了抗L1反应。