中国农业科学 ›› 2012, Vol. 45 ›› Issue (11): 2288-2294.doi: 10.3864/j.issn.0578-1752.2012.11.019

• 兽医 • 上一篇    下一篇

禽戊型肝炎病毒中国分离株ORF3蛋白的真核表达与抗原性分析

 胡守彬, 赵钦, 赵菲菲, 肖一红, 周恩民   

  1. 1.山东农业大学动物科技学院预防兽医系免疫生物学实验室,山东泰安 271018
    2.西北农林科技大学兽医免疫学研究所/西北农林科技大学动物医学院,陕西杨凌 712100
  • 收稿日期:2011-09-20 出版日期:2012-06-01 发布日期:2012-03-23
  • 通讯作者: 通信作者肖一红,E-mail:y000173@sdau.edu.cn;通信作者周恩民,E-mail:zhouem@nwsuaf.edu.cn
  • 作者简介:胡守彬,E-mail:hushoubin1234@126.com。通信作者肖一红,E-mail:y000173@sdau.edu.cn
  • 基金资助:

    山东省“泰山学者”建设工程项目(040-72010)

Eukaryotic Expression and Antigencity Analysis of Avian Hepatitis E Virus ORF3 Protein from China Isolate

 HU  Shou-Bin, ZHAO  Qin, ZHAO  Fei-Fei, XIAO  Yi-Hong, ZHOU  恩Min   

  1. 1.山东农业大学动物科技学院预防兽医系免疫生物学实验室,山东泰安 271018
    2.西北农林科技大学兽医免疫学研究所/西北农林科技大学动物医学院,陕西杨凌 712100
  • Received:2011-09-20 Online:2012-06-01 Published:2012-03-23

摘要: 【目的】为获得禽戊型肝炎病毒(hepatitis E virus, HEV)中国分离株(CaHEV)ORF3基因重组蛋白,并对其抗原性进行分析。【方法】提取CaHEV总RNA,通过RT-PCR获得ORF3基因,构建重组质粒pFastBac-HTB-ORF3,转座DH10Bac感受态细胞,提取重组杆粒Bacmid-ORF3,转染sf9细胞,用SDS-PAGE、IFA和Western blot对重组蛋白表达进行鉴定。优化表达条件,将纯化的ORF3蛋白免疫小鼠制备多克隆抗体,用制备的多抗分别与截短表达的3段CaHEV ORF3蛋白进行Western blot和ELISA检测,分析ORF3蛋白的抗原表位区。【结果】SDS-PAGE、Western blot和IFA 结果表明CaHEV ORF3蛋白被成功表达且存在细胞内,昆虫细胞在接毒后4天表达量最高。将ORF3重组蛋白免疫小鼠,利用间接ELISA方法,对制备的多抗倍比稀释检测,效价达到104,Western blot 和ELISA分析表明ORF3蛋白C端74—88氨基酸处具有较强的抗原性。【结论】本试验用Bac-to-bac系统成功构建含有CaHEV ORF3基因的重组杆状病毒,并在昆虫细胞中得到表达,其主要抗原表位位于C端74—88氨基酸,为进一步研究禽HEV ORF3的蛋白结构和功能奠定了基础。

关键词: 禽戊型肝炎病毒中国分离株, ORF3蛋白, 真核表达, 抗原性

Abstract: 【Objective】The objective of the study is to obtain recombinant protein of avian hepatitis E virus (HEV) ORF3 of China isolate (CaHEV) and analyze its antigencity. 【Method】Total RNA was extracted from CaHEV and ORF3 gene was amplified by RT-PCR and cloned into pFastBac-HT. The recombinant plasmid was transformed into DH10Bac and transfected into sf9 insect cells to express the recombinant ORF3 protein. The recombinant ORF3 protein was identified by SDS-PAGE, Western bolt and IFA methods. The purified ORF3 protein was used to immunize Balb/c mice to produce polyclonal antibodies and then to analyze the epitopes in ORF3 using 3 truncated ORF3 proteins 【Result】The results showed that ORF3 protein was expressed with the highest expression level at 4 days post inoculation. The titer of anti-ORF3 polyclonal antibodies was 104 determined with the ELISA method. The dominant epitopes of ORF3 were located between amino acids 74 and 88 in C-terminal region.【Conclusion】 Recombinant ORF3 protein from avian HEV China isolate was expressed successfully and the dominant epitopes were located between amino acids 74 and 88 in C-terminal region. These results paved a way for future study of the structure and function of ORF3 protein.

Key words: China avian hepatitis E virus, ORF3, eukaryotic expression, antigenicity