Northeastern Science Inspection Station, China Ministry of Agriculture Key Laboratory of Animal Pathogen Biology, Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northeast Agricultural University, Harbin, China.
Heilongjiang Province Center for Disease Control and Prevention, Department of Radiological Protection, Harbin, China.
Viral Immunol. 2019 Nov;32(9):393-401. doi: 10.1089/vim.2019.0071. Epub 2019 Oct 9.
Bovine rotavirus (BRV) is one of main pathogens responsible for diarrhea, fever, and vomiting. In this study, we developed a colloidal gold immunochromatographic test strip for detecting BRV according to the principle of double-antibody sandwich. The monoclonal antibodies (mAbs) and polyclonal antibodies (pAbs) were prepared and purified. On the strip, the purified mAbs labeled with the colloidal gold were used as the detector, and the goat anti-mouse antibodies and purified pAbs were coated on the nitrocellulose membranes as the control line and the test line, respectively. We optimized different reaction conditions, including the amount of mAbs, the pH of colloidal gold solution, coating solution, blocking solution, sample pad treatment solution, antibody concentration in control line, and antibody concentration in detection line. In specificity assay, the strip had high specificity in detecting BRV. No cross-reaction was observed in detecting other viruses. The detection sensitivity of the strip was found to be 1 × 10 TCID/0.1 mL. Two hundred twenty clinical samples were detected with the strip compared to reverse transcription-polymerase chain reaction. No false-negative or false-positive results were found, and the results obtained by the two methods were similar. In conclusion, we developed a novel immunochromatographic strip to rapidly detect BRV. The strip developed exhibited high sensitivity and specificity for BRV detection. It could be a rapid, convenient, and effective method for the rapid diagnosis of BRV infection in the fields.
牛轮状病毒(BRV)是引起腹泻、发热和呕吐的主要病原体之一。本研究根据双抗体夹心原理,制备并纯化单克隆抗体(mAbs)和多克隆抗体(pAbs),研制了检测 BRV 的胶体金免疫层析试纸条。在试带上,标记胶体金的纯化 mAbs 用作检测线,羊抗鼠抗体和纯化的 pAbs 分别包被在硝酸纤维素膜上作为控制线和检测线。我们优化了不同的反应条件,包括 mAbs 的用量、胶体金溶液的 pH 值、包被液、封闭液、样品垫处理液、控制线中的抗体浓度和检测线中的抗体浓度。在特异性试验中,该试纸条对 BRV 的检测具有很高的特异性,对其他病毒无交叉反应。该试纸条的检测灵敏度为 1×10TCID/0.1mL。用该试纸条检测了 220 份临床样本,并与逆转录-聚合酶链反应(RT-PCR)进行了比较。未发现假阴性或假阳性结果,两种方法的结果相似。综上所述,我们成功研制了一种快速检测 BRV 的胶体金免疫层析试纸条。该试纸条对 BRV 的检测具有较高的灵敏度和特异性,可作为 BRV 感染快速诊断的一种快速、简便、有效的方法。