Li Jiaxuan, Zang Mingxin, Xie Shuangyu, Jiang Yanping, Cui Wen, Xu Yigang, Liu Min, Qiao Xinyuan, Wang Li, Zhou Han, Li Yijing, Tang Lijie
College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, Heilongjiang, China.
Sheng Wu Gong Cheng Xue Bao. 2017 Aug 25;33(8):1284-1291. doi: 10.13345/j.cjb.170121.
To develop a clinical diagnosis technique for bluetongue virus infection, we established serotype-specific methods to detect serotype 4 of bluetongue virus (BTV-4). Two monoclonal antibodies (mAbs) against VP2 protein of BTV-4, named 4A-1G7 and 4B-1B6, were used as competitive antibodies in the competitive enzyme-linked immunosorbent assays (C-ELISA). We detected 50 negative serum samples from sheep, goats and cattle by C-ELISA. The cut-off values of 4A-1G7 and 4B-1B6 mAbs were 49% and 40%, respectively. The results of the sensitivity, specificity and repeatability by detecting standard positive serum, were consistent with the general standard of Office International Des Epizooties. Furthermore, serum samples of BTV-4, BTV-18 and BTV-20 infection could be screened out through the combined C-ELISAs by 4A-1G7 and 4B-1B6 mAbs. Thus, this technique may diagnose BTV-4, BTV-18 and BTV-20 infections.
为开发一种蓝舌病毒感染的临床诊断技术,我们建立了检测蓝舌病毒4型(BTV-4)的血清型特异性方法。两种针对BTV-4 VP2蛋白的单克隆抗体(mAb),命名为4A-1G7和4B-1B6,在竞争酶联免疫吸附试验(C-ELISA)中用作竞争抗体。我们通过C-ELISA检测了来自绵羊、山羊和牛的50份阴性血清样本。4A-1G7和4B-1B6单克隆抗体的临界值分别为49%和40%。通过检测标准阳性血清得出的敏感性、特异性和重复性结果符合国际兽疫局的一般标准。此外,通过4A-1G7和4B-1B6单克隆抗体联合C-ELISA可筛选出BTV-4、BTV-18和BTV-20感染的血清样本。因此,该技术可诊断BTV-4、BTV-18和BTV-20感染。