Department of Bioengineering, Guangdong Province Engineering Research Center for Antibody Drug and Immunoassay, Jinan University, Guangzhou, 510632, People's Republic of China.
State Key Laboratory of Food Safety Technology for Meat Products, Xiamen Yinxiang Group Co. Ltd, Xiamen, 361100, People's Republic of China.
Anal Bioanal Chem. 2021 Sep;413(23):5799-5810. doi: 10.1007/s00216-021-03558-3. Epub 2021 Jul 31.
Porcine reproductive and respiratory syndrome virus (PRRSV) has caused worldwide economic losses in the swine industry. Pigs infected with highly pathogenic (HP)-PRRSV display more severe symptoms than those infected with classical (C)-PRRSV. A rapid, sensitive, and reliable detection method to distinguish between HP-PRRSV and C-PRRSV is needed. In this study, we prepared a monoclonal antibody from a hybridoma that can distinguish HP-PRRSV(including TP, QJ, LQ, JN-HS, and TY strain) from C-PRRSV (CH-1A strain) using cell surface-fluorescence immunosorbent assays (CSFIA). Based on this monoclonal antibody (4D5), we developed a europium microsphere-based lateral flow immunochromatographic strip (EuNPs-LFICS) for the differential diagnostic detection of HP-PRRSV and C-PRRSV. Under optimized conditions, the method was rapid (15 min), sensitive (LOD: 2.57 ng mL, 606 TCID50/0.1 mL), selective for HP-PRRSV detection, and quantitative (DLR: 3.56-228 ng mL). In clinical samples, the EuNPs-LFICS assay was largely consistent with PCR results, indicating its practical clinical application.
猪繁殖与呼吸综合征病毒(PRRSV)已在全球范围内给养猪业造成了经济损失。感染高致病性(HP)-PRRSV 的猪比感染经典(C)-PRRSV 的猪表现出更严重的症状。因此,需要一种快速、灵敏、可靠的检测方法来区分 HP-PRRSV 和 C-PRRSV。本研究中,我们使用细胞表面荧光免疫吸附试验(CSFIA)从一株能区分 HP-PRRSV(包括 TP、QJ、LQ、JN-HS 和 TY 株)和 C-PRRSV(CH-1A 株)的杂交瘤中制备了一种单克隆抗体。基于该单克隆抗体(4D5),我们开发了一种基于铕纳米微球的侧向流动免疫层析试纸条(EuNPs-LFICS),用于 HP-PRRSV 和 C-PRRSV 的鉴别诊断检测。在优化条件下,该方法快速(15 min)、灵敏(LOD:2.57 ng mL,606 TCID50/0.1 mL)、对 HP-PRRSV 检测具有选择性,且可定量(DLR:3.56-228 ng mL)。在临床样本中,EuNPs-LFICS 检测方法与 PCR 结果基本一致,表明其具有实际的临床应用价值。