Cao Shengliang, Cai Xinna, Tan Min, Sun Fachao, Wang Yuchao, Shang Yingli, Liu Sidang, Xiao Yihong
Department of Fundamental Veterinary Medicine, College of Animal Science and Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an, 271018, Shandong, China.
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, Shandong, China.
Arch Virol. 2018 Feb;163(2):411-418. doi: 10.1007/s00705-017-3625-5. Epub 2017 Nov 2.
Porcine reproductive and respiratory syndrome virus (PRRSV) causes great economic losses to the swine industry worldwide. Typically, an N protein-coated indirect enzyme-linked immunosorbent assay (N-coated iELISA) is used to detect PRRSV antibodies. Non-structural protein (NSP) 4 is essential to the PRRSV life cycle and contains B-cell epitopes. Yet, no specific antibody against NSP4 has been detected in clinical samples. In this study, we developed an NSP4-coated iELISA and compared its effectiveness with the N-coated iELISA. The NSP4-coated iELISA was developed with a cut-off value of 0.406 at an optical density of 450 nm by testing a panel of 70 PRRSV positive and 80 PRRSV negative pig serum samples, which generated a specificity and sensitivity of 100%. Agreement between the NSP4-coated and N-coated iELISAs was 92.2%. Interestingly, 50 serum samples, mostly from pigs vaccinated with the HP-PRRSV live strain, tested positive for PRRSV antibodies with the NSP4-coated iELISA, but were negative with the N-coated iELISA. These results were further confirmed by western blot analysis and another iELISA based on the N-terminus of NSP2 (NSP2-1-coated iELISA). The agreement between the results of western blot analysis with the NSP4-coated and NSP2-1-coated iELISA analyses were 92% and 96.1%, respectively, showing that the developed NSP4-coated iELISA is a useful tool to discriminate a false negative from a true negative response to the HP-PRRSV vaccine.
猪繁殖与呼吸综合征病毒(PRRSV)给全球养猪业造成了巨大的经济损失。通常,采用N蛋白包被的间接酶联免疫吸附测定法(N包被iELISA)来检测PRRSV抗体。非结构蛋白(NSP)4对PRRSV的生命周期至关重要,且含有B细胞表位。然而,在临床样本中尚未检测到针对NSP4的特异性抗体。在本研究中,我们开发了一种NSP4包被的iELISA,并将其有效性与N包被的iELISA进行比较。通过检测70份PRRSV阳性和80份PRRSV阴性猪血清样本,开发出了NSP4包被的iELISA,其在450nm光密度下的临界值为0.406,特异性和敏感性均为100%。NSP4包被的iELISA与N包被的iELISA之间的一致性为92.2%。有趣的是,50份血清样本(大多来自接种高致病性PRRSV活毒株疫苗的猪),用NSP4包被的iELISA检测PRRSV抗体呈阳性,但用N包被的iELISA检测呈阴性。蛋白质印迹分析和另一种基于NSP2 N端的iELISA(NSP2-1包被的iELISA)进一步证实了这些结果。蛋白质印迹分析结果与NSP4包被的iELISA分析结果之间的一致性为92%,与NSP2-1包被的iELISA分析结果之间的一致性为96.1%,表明所开发的NSP4包被的iELISA是区分对高致病性PRRSV疫苗假阴性和真阴性反应的有用工具。