期刊文献+

亚洲Ⅰ型口蹄疫病毒双拷贝VP1基因的串联表达及其免疫原性 被引量:6

Tandem Expression and Immunogenicity of Two Copies VP1 Gene of FMDV Serotype Asia 1
下载PDF
导出
摘要 口蹄疫病毒(FMDV)VP1基因含有T细胞和B细胞表位,是口蹄疫病毒的主要免疫原性基因。作者将亚洲Ⅰ型FMDV VP1基因首尾串联构建双拷贝的VP1基因(2VP1),实现双拷贝VP1基因的原核表达,表达的重组蛋白(GST2VP1)经Sephadex-G200分子筛层析纯化后,Western blot证实其有反应原性,动物试验表明重组蛋白在加强免疫后能够产生和灭活疫苗相当的ELISA抗体和中和抗体;本试验结果为亚洲Ⅰ型FMDV免疫原性研究及GST2VP1蛋白的进一步应用奠定了基础。 VP1 gene of foot-and-mouth disease virus (FMDV) is the major immunogenic gene as it contains T cell and B cell epitopes. In this study, we constructed a recombinant expressing plasmid(KG2VP1) including two VP1 genes(2VP1) of Asia 1 FMDV, and the 2VP1 gene was expressed in E. coli BL21. The fusional protein (GST2VP1) which was purified by Sephadex-G200 sieve chromatography demonstrated the reactionogenicity by Western blot. And the mice test indicated that the GST2VP1 can induce similar levels of ELISA and neutralization antibody like inactivated vaccine. We provide foundation for researching the immunogenicity of FMDV serotype Asia 1 and further application of GST2VP1 in future.
出处 《畜牧兽医学报》 CAS CSCD 北大核心 2009年第3期383-387,共5页 ACTA VETERINARIA ET ZOOTECHNICA SINICA
基金 国家科技支撑计划(2006BAD06A18) 农业科技成果转化资金(03EFN217100315)
关键词 亚洲Ⅰ型口蹄疫病毒 2VP1 串联表达 免疫原性 Asia 1 FMDV 2VP1 gene tandem expression immunogenicity
  • 相关文献

参考文献14

  • 1DOMINGO E, ESCARMIS C, BARONOWSKI E, et al. Evolution of foot-and-mouth disease virus[J].Virus Research, 2003,91(1) :47-63.
  • 2KNOWLES N J, SAMUEL A R. Molecular epidemiology of foot-and-mouth disease virus[J]. Virus Research 2003, 91(1): 65-80.
  • 3中国内地部分地区发生亚洲1型口蹄疫疫情[J].畜牧兽医学报,2005,36(6):589-589. 被引量:2
  • 4中华人民共和国农业部.兽医公告[EB/OL].http://www.agri.gov.cn/ztzl/sygb/
  • 5SURYANARAYANA V V S, VISWANATHAN S, RATISH G, et al. E. coli expressed proteins as diagnostic reagents for typing of Foot-and-mouth disease virus[J]. Archives of Virology, 1999, 144 : 1701-1712.
  • 6KLEID D G, YANSURA D, SMALL B, et al. Cloned viral protein vaccine for foot-and-mouth disease: responses in cattle and swine[J].Science, 1981,214 : 1125-1129.
  • 7FOX G, PARRY N, BARNETT P V, et al. The cell attachment site on foot-and-mouth disease virus includes the amino acid sequence RGD(arginine-glycineaspartic acid)[J]. Journal of General Virology, 1989,70:625-637.
  • 8WANGJ L, LIU M Q, HAN J,et al. A peptide of foot-and-mouth disease virus serotype Asia 1 generating a neutralizing antibody response, and an immunostimulatory peptide[J]. Veterinary Microbiology, 2007,125: 224-231.
  • 9萨姆布鲁克J 弗里奇EF 曼尼阿蒂斯T 金冬雁 黎孟枫 译.分子克隆实验指南[M]:第2版[M].北京:科学出版社,1998.19-21.
  • 10MARQUARDT O, RAHMAN M M, FREIBERG B. Genetic and antigenic variance of foot-and-mouth disease virus type Asial[J]. Archives of Virology, 2000,145(1):149-157.

共引文献16

同被引文献74

  • 1中国内地部分地区发生亚洲1型口蹄疫疫情[J].畜牧兽医学报,2005,36(6):589-589. 被引量:2
  • 2独军政,常惠芸,丛国正,林彤,邵军军,魏小娟,刘在新,谢庆阁.Asia1型口蹄疫病毒VP1基因的克隆、原核表达及纯化[J].畜牧兽医学报,2005,36(6):631-634. 被引量:4
  • 3张秀艳,何国庆.蛋白质突变体基因库构建方法的研究进展[J].中国生物工程杂志,2006,26(10):52-58. 被引量:5
  • 4金春梅,许应天,张守发,鲁承,于龙政.牛瑟氏泰勒虫P33表面蛋白基因的克隆与序列分析[J].中国预防兽医学报,2007,29(2):112-114. 被引量:8
  • 5HAJJAR K A, KRISHNAN S. Annexin Ⅱ : a mediator of the plasmin/plasminogen activator system[J]. Trends Cardiovasc Med, 1999, 9 : 128-138.
  • 6HAYES M J, SHAO D, BAILLY M, et al. Regulation of actin dynamics bv annexin 2[J]. EMBO J,2006, 25:1816-1826.
  • 7GERKE V, CREUTZ C E, MOSS S E. Annexins: linking Ca^2+ signalling to membrane dynamics[J]. Nature Rev Mol Cell Biol, 2005, 6:449-461.
  • 8HAYES M J, RESCHER U, GERKE V, et al. Annexin-actin interactions[J]. Traffic, 2004, 5 (8): 571-576.
  • 9RAYNAL P, POLLARD H B. Annexins: the problem of assessing the biological role for a gene family of multifunctional calcium- and phosphohpid-binding proteins[J]. Biochim Biophys Acia Rev Biomembr, 1994, 1197:63-93.
  • 10SARIS C J, TACK B F, KRISTENSEN T, et al. The cDNA sequence for the protein-tyrosine kinase substrate p36 (calpactin Ⅰ heavy chain) reveals a multidomain protein with internal repeats [ J ]. Cell, 1986, 46:201-212.

引证文献6

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部