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日本血吸虫新基因Sj-MA的克隆、表达及保护性免疫
引用本文:陈欲晓,易新元,曾宪芳,袁仕善,张顺科,MCRYENOLDS Larry.日本血吸虫新基因Sj-MA的克隆、表达及保护性免疫[J].生物化学与生物物理学报,2003,35(11):981-985.
作者姓名:陈欲晓  易新元  曾宪芳  袁仕善  张顺科  MCRYENOLDS Larry
作者单位:中南大学湘雅医学院免疫学教研室,中南大学湘雅医学院寄生虫学教研室,中南大学湘雅医学院寄生虫学教研室,中南大学湘雅医学院寄生虫学教研室,中南大学湘雅医学院寄生虫学教研室,Molecular Parasitology Group,New England Biolabs,Inc.,Beverly,MA01915 长沙410078,长沙410078,长沙410078,长沙410078,长沙410078
基金项目:世界卫生组织 /热带病研究与训练规划署 (WHO/TDR)资助项目 (No .980 2 68)~~
摘    要:为发现新基因 ,寻找日本血吸虫病新疫苗候选分子 ,采用Sj雄虫免疫血清筛选Sj成虫cDNA文库。经测序发现新基因Sj MA含有一个完整的阅读框 ,推测其由 2 4 9个氨基酸组成 ,编码分子量为 2 8.8kD的可溶性蛋白质 ,并带有多个能被磷酸化激活的位点 ,提示其可能为一重要的信息传递分子。将Sj MA的cDNA亚克隆至原核表达载体pGEX 5X ,获得Sj MA原核表达的重组体rSj MA/GST ,并在E .coli中高效表达为谷胱甘肽S 转移酶 (GST)融合蛋白 ,分子量为 5 4 .8kD ,Western印迹显示融合蛋白质能被抗雄虫和抗GST血清识别。融合蛋白质免疫小鼠可诱导 34.2 9%的减虫率 ,与对照组有显著性差异 (P <0 .0 0 1 )。表明新基因Sj MA表达的蛋白质能诱导小鼠的抗日本血吸虫的保护性免疫 ,提示其作为日本血吸虫疫苗候选分子的潜在价值

关 键 词:免疫筛选  日本血吸虫  雄虫  表达

Molecular Cloning, Expression and Vaccination of a Novel Gene Sj-MA of Schistosoma japonicum
CHEN Yu Xiao,YI Xin Yuan ,ZENG Xian Fang ,YUAN Shi Shan ,ZHANG Shun Ke ,MCREYNOLDS Larry.Molecular Cloning, Expression and Vaccination of a Novel Gene Sj-MA of Schistosoma japonicum[J].Acta Biochimica et Biophysica Sinica,2003,35(11):981-985.
Authors:CHEN Yu Xiao  YI Xin Yuan  ZENG Xian Fang  YUAN Shi Shan  ZHANG Shun Ke  MCREYNOLDS Larry
Institution:CHEN Yu Xiao,YI Xin Yuan 1*,ZENG Xian Fang 1,YUAN Shi Shan 1,ZHANG Shun Ke 1,MCREYNOLDS Larry 2
Abstract:In order to obtain new gene and to develop the new vaccine candidate of immunoprotection against Schistosoma japonicum (Sj), Sj adult worm cDNA library was screened with anti sera to soluble male adult worm antigen and resulted in the discovery of a novel gene designated as Sj MA. Sequence analysis showed that Sj MA as a complete cDNA contains one open reading frame. It was deduced to contain 249 amino acid residues and encode a 28.8 kD soluble protein with plenty of phosphorylation sites, supposing its action in signal transduction. Furthermore, Sj MA cDNA was cloned into a prokaryotic expression vector pGEX 5X to construct the recombinant plasmid which was transformed and highly expressed in E. coli as a 54.8 kD glutathione S transferase (GST) fusion protein. The fusion protein rSj MA/GST could be recognized with both anti male adult worm sera and anti GST sera in Western blotting. Mice vaccinated with the fusion protein revealed significant worm reduction rate of 34.29% (P<0.001), compared with the control groups. Taken together, the novel gene Sj MA can be expressed in E.coli as a fusion protein that can elicit immunity against Schistosoma japonicum, suggesting its potential as a new vaccine candidate.
Keywords:immunoscreening  Schistosoma japonicum  male adult worm  expression
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