期刊文献+

鼠疫菌免疫胶体金快速检测方法的建立 被引量:8

Development of an immunochromayography assay method for the detection of Yersinia pestis
原文传递
导出
摘要 目的利用免疫胶体金技术建立一种简便、快速并适用于基层人员使用的鼠疫菌抗原检测方法。方法将抗鼠疫菌F1抗原的抗体致敏硝酸纤维素膜,用于捕获鼠疫抗原,然后用免疫胶体金颗粒进行标记。结果应用鼠疫菌免疫胶体金快速检测法最低可检出不同鼠疫菌(EV和Evp株)1.56×105CFU/ml,检测鼠疫菌F1抗原最低可检出1ng/ml,与鼠疫反向间接血凝法的检测结果一致;并且不与假结核小肠结肠炎等耶尔森菌以及其他相关细菌发生交叉反应。结论鼠疫菌免疫胶体金快速检测法具有较好的特异性、敏感性和简便快速的特点。 Objective To develop a method of imrnunochromatography assay(ICA) with sensitive, specific,rapid, simple and suitable for the detection of Yersinia pestis antigen at the local laboratories. Methods Colloidal gold labeled with the anti-Fl antibody of Yersinia pestis, was connnected with the anti-F1 antibody of Yersinia pestis to pyroxylin membrane and assembled them to the dipstick of ICA. Results Results showed that the rates of sensitivity for F1 antigen and Yersinia pestis were 1 ng/ml and 1.56 × 10^5 CFU/ml respectively. However, Yersinia pseudotuberculosis et al could not be detected by dipstick MICA. Conclusion The method of ICA appeared to be consistent to those of r-IHA with better specificity and sensitivity but was simple and rapid for the detection of Yersinia pestis and F1 antigen.
出处 《中华流行病学杂志》 CAS CSCD 北大核心 2006年第3期253-255,共3页 Chinese Journal of Epidemiology
关键词 鼠疫菌 鼠疫菌F1抗原 胶体金 免疫层析 Yersinia pestis F1 antigen Colloidal gold Immunochromatography assay
  • 相关文献

参考文献4

  • 1Splettstoesser WD,Rahalison L,Grunow R,et al.Evaluation of a standardized Fl capsular antigen capture ELISA test kit for the rapid diagnosis of plague FEMS.Immunol Med Microbiol,2004,41:149-155.
  • 2Thullier P,Guglielmo V,Rajerison M,et al.Short report:Serodiagnosis of plague in humans and rats using a rapid test.Am J Trop Med Hyg,2003,69:450-451.
  • 3Rahalison L,Vololonirina E,Ratsitorahina M,et al.Diagnosis of bubonic plague by PCR in Madagascar under field conditions.J Clin Microbiol,2000,38:260-263.
  • 4Chanteau S,Rahalison L,Ratsitorahina M,et al.Early diagnosis of bubonic plague using F1 antigen capture ELISA assay and rapid immunogold dipstick.Int J Med Microbiol,2000,290:279-283.

同被引文献81

引证文献8

二级引证文献32

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