Chu Jia-Qi, Hu Xu-Min, Kim Myung-Cheol, Park Chang-Sik, Jun Moo-Hyung
College of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.
J Microbiol. 2009 Oct;47(5):582-8. doi: 10.1007/s12275-009-0033-x. Epub 2009 Oct 24.
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.
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。