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Development of a recombinant TaSP-based Dot-ELISA for detection of Theileria annulata infection in cattle

机译:基于重组TASP的DOT-ELISA检测牛中的TheLeria Annulata感染

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The study was conducted to develop and validate Dot-ELISA for the diagnosis of Theileria annulata infection in cattle using recombinant Theileria annulata surface protein (r-TaSP). The r-TaSP based indirect plate-ELISA was used as a reference test to compare the efficacy of the Dot-ELISA. The Dot-ELISA was optimized with 500 ng of antigen per dot, 1:150 dilution of serum and 1:1000 dilution of secondary antibody for positive and negative reaction. A total of 17 confirmed positive, 25 negative and 129 field sera samples were used to calculate the diagnostic accuracy of Dot-ELISA in comparison with indirect plate-ELISA. The diagnostic sensitivity and specificity of the Dot-ELISA was 95.8 per cent (95% CI, 93.1-97.2) and 80 per cent (95% CI, 48.1-96.2), respectively. The positive predictive value (PPV) of Dot-ELISA was 98.2 percent (95% CI, 95.5-99.7) and negative predictive value (NPV) was 61.6 percent (95% CI, 37-74). The positive and negative likelihood ratios were 4.79 (95% CI, 1.8-25.69) and 0.053 (95% CI 0.03-1.4), respectively. The Dot-ELISA showed moderate agreement (k value, 0.67, 95% CI, 0.36- 0.82) with indirect plate-ELISA. The developed Dot-ELISA is less expensive and convenient for the diagnosis of T. annulata infection in cattle under field conditions.
机译:该研究进行了开发和验证DOT-ELISA,用于使用重组Theileria Annulata蛋白(R-Task)诊断牛中吞咽植物感染的诊断。基于RASP的间接板-ELISA用作参考测试,以比较DOT-ELISA的功效。 DOT-ELISA用每点500 ng抗原进行优化,1:150稀释血清和1:1000稀释的二抗,用于正面和负反应。总共17个确认的阳性,25个阴性和129个血清样品用于计算DOT-ELISA的诊断准确性与间接板-ELISA相比。 DOT-ELISA的诊断敏感性和特异性分别为95.8%(95%CI,93.1-97.2)和80%(95%CI,48.1-96.2)。 DOT-ELISA的阳性预测值(PPV)为98.2%(95%CI,95.5-99.7)和阴性预测值(NPV)为61.6%(95%CI,37-74)。阳性和负似然比分别为4.79(95%CI,1.8-25.69)和0.053(95%CI 0.03-1.4)。 DOT-ELISA显示间接板 - ELISA的中等协议(K值,0.67,95%CI,0.36- 0.82)。开发的DOT-ELISA昂贵且方便地诊断牛在牛下的现场条件下的吞咽感染。

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