畜牧兽医学报 ›› 2012, Vol. 43 ›› Issue (3): 446-452.doi:

• 预防兽医 • 上一篇    下一篇

表达牛源犬新孢子虫NcSRS2基因重组腺病毒的构建及免疫原性分析

贾立军,于龙政,张守发*   

  1. 延边大学农学院动物医学系,延吉 133002
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2012-03-28 发布日期:2012-03-28
  • 通讯作者: 张守发

Construction of a Recombinant Adenovirus Expressing NcSRS2 Protein of Bovine Neospora Caninum and Immunogenicity Analysis of the Protein

JIA Lijun, YU Longzheng, ZHANG Shoufa*   

  1. Department of Veterinary Medicine, Agriculture College of Yanbian University, Yanji 133002, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2012-03-28 Published:2012-03-28
  • Contact: ZHANG Shoufa

摘要: 为构建牛源犬新孢子虫NcSRS2基因重组腺病毒,并分析其免疫原性, PCR扩增牛源犬新孢子虫NcSRS2基因,构建克隆质粒pMD18TNcSRS2、重组腺病毒穿梭质粒pCR259NcSRS2及表达质粒TransposeAdNcSRS2,脂质体介导转染QBIHEK293细胞,包装重组腺病毒Ad5NcSRS2,PCR检测重组腺病毒NcSRS2基因,IFAT和Western blotting检测NcSRS2基因在QBIHEK293细胞中的表达,测定病毒滴度后,收集病毒液免疫BALB/c小鼠,间接ELISA检测小鼠血清IgG抗体水平。结果显示,扩增的牛源犬新孢子虫NcSRS2基因大小为1 227 bp,与GenBank中发表的NcSRS2(AF061249)核苷酸序列相似性为99%;重组腺病毒Ad5NcSRS2在293细胞中包装成功,表达蛋白的相对分子质量为43 ku,具有较好的反应原性;测得重组腺病毒Ad5NcSRS2滴度为109TCID50·mL-1,间接ELISA检测二免后3周BALB/c小鼠血清中IgG抗体效价达1∶2 048。本研究成功构建了具有良好免疫原性的重组腺病毒Ad5NcSRS2,为牛源犬新孢子虫NcSRS2基因重组腺病毒载体疫苗的研制奠定了基础。

Abstract: In order to construct a recombinant adenovirus expressing NcSRS2 protein of bovine Neospora Caninum, NcSRS2 gene of bovine Neospora Caninum was amplified by PCR, pMD18TNcSRS2, pCR259NcSRS2 and TransposeAdNcSRS2 were constructed in this research. Coated with liposome, TransposeAdNcSRS2 was transfected into QBIHEK293 cells to package recombinant adenovirus Ad5NcSRS2. Recombinant adenovirus NcSRS2 gene was detected by PCR. The expression of NcSRS2 gene in QBIHEK293 cells was detected by IFAT and Western blotting. After the virus titer was determined, the virus fluid was collected to inoculate BALB/c mice and IgG antibody levels in the sera were measured by indirect ELISA. The size of NcSRS2 gene was 1 227 bp. The nucleotide sequence of the gene shared 99% homology with that in GenBank (AF061249). Recombinant adenovirus Ad5NcSRS2 was successfully packaged in 293 cells. The protein expressed by Ad5NcSRS2 was 43 kD and had good reactogenicity. The titer of recombinant adenovirus Ad5NcSRS2 was 109TCID50·mL-1. Three weeks post the second immunization, IgG antibody titers in the sera of BALB/c mice were up to 1:2 048, measured by indirect ELISA. A recombinant adenovirus Ad5NcSRS2 which have good immunogenicity was successfully constructed. This settles a solid foundation for the development of recombinant adenovirus vaccine against Neospora Caninum based on NcSRS2 gene.