中国农业科学 ›› 2010, Vol. 43 ›› Issue (20): 4303-4309 .doi: 10.3864/j.issn.0578-1752.2010.20.023

• 兽医 • 上一篇    下一篇

牛呼吸道合胞体病毒重组N蛋白间接ELISA方法的建立及应用

王红,余丽芸,侯喜林,朴范泽,翟延庆

  

  1. (黑龙江八一农垦大学动物科技学院)
  • 收稿日期:2009-05-04 修回日期:2010-04-08 出版日期:2010-10-15 发布日期:2010-10-15
  • 通讯作者: 侯喜林

Development of an Indirect ELISA Diagnostic Method for Detecting Bovine Respiratory Syncytial Virus Using Recombinant Nucleocapsid Protein and Its Preliminary Application

WANG Hong, YU Li-yun, HOU Xi-lin, PIAO Fan-ze, ZHAI Yan-qing
  

  1. (黑龙江八一农垦大学动物科技学院)
  • Received:2009-05-04 Revised:2010-04-08 Online:2010-10-15 Published:2010-10-15
  • Contact: HOU Xi-lin

摘要:

【目的】以纯化的牛呼吸道合胞体病毒(BRSV)HJ株重组N蛋白作为包被抗原,对各项条件进行优化,确定判定标准,建立检测BRSV抗体的间接ELISA方法。【方法】将已构建的重组菌BL21(DE3)进行诱导表达,获得重组N蛋白。利用电洗脱法对表达产物进行纯化,并用Western blot对表达产物进行鉴定。以纯化后的重组N蛋白作为诊断抗原,对ELISA反应条件进行优化,初步建立检测BRSV抗体的间接ELISA诊断方法。【结果】成功表达并纯化了BRSV HJ株重组N蛋白,Western blot检测结果证明表达产物具有良好的反应原性。以重组N蛋白作为诊断抗原,建立了间接ELISA诊断方法。交叉试验结果表明重组N蛋白与牛无浆体病(Anaplasmosis)、牛传染性鼻气管炎(IBRV)和牛副流感(BPIV)阳性血清均不发生交叉反应。与中和试验(SNT)相比较,该方法的特异性、敏感性和符合率分别为85.0%、90.9%和87.7%。采用本试验建立的间接ELISA方法对黑龙江省的牡丹江、佳木斯、鹤岗和大庆4个地区牛场的600份牛血清进行了检测,结果表明,黑龙江省部分地区BRSV的抗体阳性率为27.33%。【结论】本研究建立的间接ELISA方法具有较好的特异性、敏感性和重复性,利用该方法初步证实黑龙江省部分地区存在牛呼吸道合胞体病。这一研究为牛呼吸道合胞体病诊断试剂盒的研制奠定了基础,并为该病的诊断与流行病学调查提供有效的技术手段。

关键词: 牛呼吸道合胞体病毒, 重组N蛋白, 间接ELISA, 初步应用

Abstract:

【Objective】 The ELISA plate was coated with the purified bovine respiratory syncytial virus (BRSV) HJ strain recombinant nucleocapsid (N) antigen and the optimal reaction conditions of indirect ELISA were determined by experiments. The indirect ELISA method for detecting BRSV antibody was established by determining the cut off value. 【Method】 The recombinant E.coli strain BL21 containing the recombinant plasmid pET-30a-N was induced by IPTG. The recombinant N protein was expressed at high level, then it was purified by electroelution method. The recombinant N protein was identified by western blot. Taking the purified recombinant N protein as diagnostic antigen, the indirect ELISA method for detecting BRSV antibody was established. 【Result】 The recombinant N protein was successfully expressed and purified, it was proved that the recombinant protein has good reactogenicity by western blot. Taking the purified recombinant N protein as diagnostic antigen, the indirect ELISA method for detecting BRSV antibody was established. The results showed that there was no cross reaction between the recombinant N protein and the positive serum of Anaplasmosis, IBRV, BPIV. Compared with the serum neutralization testing, the results indicated that the specificity, sensitivity and coincidence of the developed indirect ELISA was 85.0%, 90.9% and 87.7%, respectively. A total of 600 sera of cattle, which obtained from Mudanjiang, Jamusi, Hegang, Daqing in Heilongjiang province, were tested by the developed indirect ELISA method and the positive rate was 27.33%. 【Conclusion】 The developed indirect ELISA has good specificity, sensitivity and reproducibility, it has been proved that BRSV is existed in some areas in Heilongjing province. It is very important that the development of indirect ELISA and its preliminary application of BRSV in cattle for the preparation of ELISA kit, diagnosis and epidemiological investigation of bovine respiratory syncytial disease.

Key words: bovine respiratory syncytial virus, recombinant nucleocapsid protein, indirect ELISA, preliminary application