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口蹄疫病毒表位与乙肝核心蛋白融合体在转基因烟草中的免疫原性。

Immunogenicity of the epitope of the foot-and-mouth disease virus fused with a hepatitis B core protein as expressed in transgenic tobacco.

作者信息

Huang Yahong, Liang Wanqi, Wang Yujiong, Zhou Zhiai, Pan Aihu, Yang Xinghong, Huang Cheng, Chen Jianxiu, Zhang Dabing

机构信息

School of Life Science and Technology, Shanghai Jiao Tong University, Shanghai, PR China.

出版信息

Viral Immunol. 2005;18(4):668-77. doi: 10.1089/vim.2005.18.668.

Abstract

A novel plant-based vaccine protecting against foot-and-mouth disease (FMD) was developed by inserting the VP21 epitope into the internal region of the hepatitis B virus core antigen gene (HBcAg). The specific sequence of the VP21 epitope is located within the VP1 capsid protein of the FMD virus (FMDV). It spans 21 amino acids located between positions 140 and 160 of the G-H loop. The fusion gene, HBCVP, was inserted into the plant binary vector pBI121 and then transformed into tobacco (Nicotiana tabacum) plants via Agrobacterium tumefaciens strain LBA 4404. The presence of HBCVP in the tobacco genome was confirmed by polymerase chain reaction (PCR); its transcription was verified by reverse transcription-PCR; and the recombinant protein expression was confirmed by Western blot analysis. The results of immunologic microscopic observation demonstrated that recombinant fusion protein HBCVP can form a virus-like particle (VLP) structure in transgenic tobacco leaves. Mice, immunized intraperitoneally with a soluble crude extract of transgenic tobacco leaves, were found to produce specific antibody responses to both HBcAg and FMDV VP1. A virus challenge demonstrated that the immunized mice were highly protected against virulent FMD. This work describes a new way to develop an FMD vaccine from plants that will aid the development of new vaccines using HBcAg fused to the conserved epitopes of other pathogenic antigens.

摘要

通过将VP21表位插入乙型肝炎病毒核心抗原基因(HBcAg)的内部区域,开发出了一种新型的预防口蹄疫(FMD)的植物源疫苗。VP21表位的特定序列位于口蹄疫病毒(FMDV)的VP1衣壳蛋白内。它跨越G-H环第140至160位之间的21个氨基酸。融合基因HBCVP被插入植物双元载体pBI121,然后通过根癌农杆菌菌株LBA 4404转化到烟草(Nicotiana tabacum)植株中。通过聚合酶链反应(PCR)确认了烟草基因组中HBCVP的存在;通过逆转录PCR验证了其转录;通过蛋白质免疫印迹分析确认了重组蛋白的表达。免疫显微镜观察结果表明,重组融合蛋白HBCVP可在转基因烟草叶片中形成病毒样颗粒(VLP)结构。用转基因烟草叶片的可溶性粗提物腹腔注射免疫的小鼠,被发现对HBcAg和FMDV VP1均产生特异性抗体反应。病毒攻击试验表明,免疫小鼠对强毒性口蹄疫具有高度的抵抗力。这项工作描述了一种从植物中开发口蹄疫疫苗的新方法,这将有助于开发使用与其他致病抗原保守表位融合的HBcAg的新型疫苗。

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