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基于重组核衣壳蛋白的酶联免疫吸附测定法检测猪繁殖与呼吸综合征病毒抗体的方法建立及验证

Development and validation of a recombinant nucleocapsid protein-based ELISA for detection of the antibody to porcine reproductive and respiratory syndrome virus.

作者信息

Chu Jia-Qi, Hu Xu-Min, Kim Myung-Cheol, Park Chang-Sik, Jun Moo-Hyung

机构信息

College of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.

出版信息

J Microbiol. 2009 Oct;47(5):582-8. doi: 10.1007/s12275-009-0033-x. Epub 2009 Oct 24.

Abstract

Three indirect enzyme-linked immunosorbent assays (iELISA) based on the North American like (NA-like), European like (EU-like) and co-expressed NA- and EU-like recombinant nucleocapsid proteins (N-protein) of porcine reproductive and respiratory syndrome virus (PRRSV) were validated for the detection of the antibodies in porcine sera. A total of 422 serum samples from unvaccinated pigs were tested. The cut-off value was optimized by a two-graph receiver operating characteristics analysis at a 95% confidence level. This assay was validated with Western blot analysis and IDEXX HerdChek ELISA. Cross-reactivity results showed that iELISA was PRRSV-specific. Repeatability tests revealed that the coefficients of variation of positive sera within and between runs were less than 10%. The results indicate that iELISA is simpler to produce and perform, time-saving and suitable for large scale surveys of PRRSV infection at low cost, and is potentially useful to evaluate the efficiency of various vaccines against PRRSV.

摘要

基于北美型(NA-like)、欧洲型(EU-like)以及共表达的猪繁殖与呼吸综合征病毒(PRRSV)北美型和欧洲型重组核衣壳蛋白(N蛋白)的三种间接酶联免疫吸附测定(iELISA)方法,经验证可用于检测猪血清中的抗体。共检测了422份未接种疫苗猪的血清样本。通过双图接收者操作特征分析在95%置信水平下优化了临界值。该测定方法经蛋白质免疫印迹分析和IDEXX HerdChek ELISA验证。交叉反应结果表明iELISA具有PRRSV特异性。重复性试验显示,批内和批间阳性血清的变异系数均小于10%。结果表明,iELISA制备和操作更简便、省时,适合低成本大规模检测PRRSV感染,并且在评估各种抗PRRSV疫苗的效力方面可能具有潜在用途。

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