中国寄生虫学与寄生虫病杂志 ›› 2001, Vol. 19 ›› Issue (5): 7-286.

• 论著 • 上一篇    下一篇

弓形虫P30基因重组质粒的构建及其免疫效果

龚娅;陈晓光;冯明钊
  

  1. 第一军医大学寄生虫学教研室;第一军医大学寄生虫学教研室;香港中文大学生物系 广州510515;中国人民解放军第157中心医院检验科广州510510;广州510515;
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2001-10-30 发布日期:2001-10-30

The Construction of Recombinant Plasmids of Toxoplasma gondii P30 and the Immunoprotective Activity of the P30 Constructs

GONG Ya 1*;CHEN Xiao guang 1;FENG Ming zhao 2   

  1. 1 Department of Parasitology;The First Military Medical University;Guangzhou 510515; 2 Department of Biology;The Chinese University of Hong Kong;
  • Received:1900-01-01 Revised:1900-01-01 Online:2001-10-30 Published:2001-10-30

摘要:   目的 通过构建含弓形虫P30不同表达形式 (膜型、分泌型及细胞内型 )的重组质粒 ,并将其用于免疫小鼠 ,测定抗体水平 ,以期初步筛选出一种对弓形虫感染具有良好保护作用的核酸疫苗。 方法 利用PCR技术和亚克隆技术分别构建弓形虫表膜型P30基因重组质粒 (含完整的P30编码序列 ,包括信号肽及疏水尾 )pcDNA3 P30Mb ,分泌型P30基因重组质粒 (含完整的P30编码序列 ,不包括疏水尾 )pcDNA3 P30Se以及细胞内型P30基因重组质粒 (含完整的P30编码序列 ,但不包括信号肽 )pcDNA3 P30In。将以上 3种重组质粒分别与脂质体混合后免疫小鼠 ,ELISA及免疫印迹测定小鼠血清中特异的IgG抗体。 结果 成功构建了弓形虫P30基因 3种表达形式的重组质粒 ,经双酶切鉴定及DNA序列测定 ,3种重组质粒中的插入片段确为P30的编码基因 ,且读码框架正确 ;抗体测定显示 :3个免疫组均能诱导小鼠产生特异的IgG抗体 ,但各组之间IgG出现的时间及强度有一定的差异。 结论 用编码弓形虫P30抗原的重组质粒进行核酸免疫 ,能诱导免疫小鼠产生特异性的IgG抗体 ;膜型及分泌型免疫小鼠的特异IgG抗体出现的时间早于细胞内型免疫鼠 ,但 4wk后 3组间差异无显著性。

关键词: 弓形虫, P30, 核酸免疫

Abstract:  Objective To identify the potential DNA vaccine candidate which can induce the protective immune response to Toxoplasma gondii by inoculating mice with plasmid DNAs encoding three different forms of P30 antigen (membranous secretory,and intracellular). Methods Three forms of recombinant plasmid: pcDNA3 P30Mb(contain the whole P30 gene sequence,including the gene encoding signal peptide and hydrophobic tail),pcDNA3 P30Se(contain the whole P30 gene sequence, without the gene encoding hydrophobic tail) and pcDNA3 P30In(contain the whole P30 gene sequence,without the gene encoding signal peptide) were constructed by PCR and subcloning technique. The mice were immunized with different forms of recombinant plasmids and IgG antibodies in the mice were detected by ELISA and Western blotting. Results Three forms of expression recombinant plasmid of Toxoplasma gondii P30 gene were successfully constructed. The P30 inserts were identified by restrictive enzyme digestion and sequencing. ELISA and Western blotting analysis demonstrated that specific IgG antibody could be induced in three immunized groups, but there was some difference in appearence time and intensity of IgG.Conclusion Genetically immunization of mice with the recombinant plasmids could elicit specific IgG antibodies. In respect to IgG response, the immune efficiency of the three forms of recombinant plasmids was different at the beginning (2 wk),but 4 wk later approximately same.

Key words: Toxoplasma gondii, P30, DNA vaccine