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[日本脑炎病毒包膜蛋白结构域III的免疫原性和抗原性]

[Immunogenicity and antigenicity of Japanese encephalitis virus envelope protein domain III].

作者信息

Huang Ying, Liu Shan, Yang Peng, Du Yun, Sun Zhiwei, Yu Weiyuan

机构信息

Laboratory for Protein Engineering, Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2009 Oct;25(10):1532-7.

Abstract

To express the domain III gene of Japanese encephalitis virus (JEV) and to learn the possibility of developing the Dil protein as a subunit vaccine, we amplified the JEV DIII gene by PCR and constructed the expression plasmid pET-JE DIII by inserting JEV DIII gene into the prokaryotic expression vector pET-32a(+). The domain III protein of the attenuated strain SA14-14-2 was expressed as a thioredoxin (Trx) fusion protein, which was unique in forming a large fraction of the soluble recombinant protein. We immunized the rabbits and mice with the purified protein, tested the antigenicity and immunogenicity of JEV DIII protein by ELISA, Western blotting, plaque reduction test and observed the protective efficacy on challenged weanling mice with JEV. Rabbits immunized with the purified JEV DIII protein generated 1: 7 x 10(5) anti-JEV specific antibody titers. BALB/c mice immunized with the purified JEV E DIII protein generated 1: 8.2 x 10(4) anti-JEV specific antibody titers. And the neutralized antibody titer can reach 1:256, the survival rate of the immunized weanling mice was approximately 75%. Overall, this study highlighted that recombinant JEV E DIII protein delivered in mice and rabbits can generate high antibody titers against JEV, and protect some mice challenged with JEV. These studies can provide useful information for further developing the domain III recombinant protein as subunit vaccine against JEV.

摘要

为表达日本脑炎病毒(JEV)的结构域III基因,并了解开发DIII蛋白作为亚单位疫苗的可能性,我们通过PCR扩增了JEV DIII基因,并将JEV DIII基因插入原核表达载体pET-32a(+)中构建了表达质粒pET-JE DIII。减毒株SA14-14-2的结构域III蛋白表达为硫氧还蛋白(Trx)融合蛋白,其独特之处在于能形成很大一部分可溶性重组蛋白。我们用纯化后的蛋白免疫兔和小鼠,通过ELISA、Western印迹、蚀斑减少试验检测JEV DIII蛋白的抗原性和免疫原性,并观察其对JEV攻击的断奶小鼠的保护效果。用纯化的JEV DIII蛋白免疫的兔产生了1:7×10(5)的抗JEV特异性抗体效价。用纯化的JEV E DIII蛋白免疫的BALB/c小鼠产生了1:8.2×10(4)的抗JEV特异性抗体效价。且中和抗体效价可达1:256,免疫的断奶小鼠存活率约为75%。总体而言,本研究强调在小鼠和兔中递送的重组JEV E DIII蛋白可产生针对JEV的高抗体效价,并保护部分受JEV攻击的小鼠。这些研究可为进一步开发结构域III重组蛋白作为抗JEV的亚单位疫苗提供有用信息。

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