Wu Zhi, Wu Shuang, Xie Jun, Lu Huipeng, Jiang Yong, Lin Mengzhou, Gu Chenyi, Zhu Shanyuan
Jiangsu Key Laboratory for High-Tech Research and Development of Veterinary Biopharmaceuticals, Engineering Technology Research Center for Modern Animal Science and Novel Veterinary Pharmaceutic Development, Jiangsu Agri-Animal Husbandry Vocational College, Taizhou 225300, China.
Acta Vet Hung. 2025 Jul 16. doi: 10.1556/004.2025.01101.
Mixed infections are a serious problem causing significant economic losses in the duck industry. Duck hepatitis A virus serotype 3 (DHAV-3), duck Tembusu virus (DTMUV) and novel duck reovirus (NDRV), belonging to the family Picornaviridae, Flaviviridae and Spinareoviridae, respectively, are important pathogens with similar symptoms in infected ducks. To detect and differentiate these viruses, this study developed a triplex real-time PCR assay targeting the VP1, E and σC genes of DHAV-3, DTMUV and NDRV, respectively. Validation tests and clinical applications followed the optimization of the triplex real-time PCR assay. The novel triplex assay showed high specificity with no cross-reactivity with eight other common duck viruses. The detection limits were 1 × 101 copies/μL for DTMUV, DHAV-3 and NDRV, with intra- and inter-assay variation coefficients (CV) below 4%. A total of 135 clinical samples were tested to evaluate the method's feasibility. The positive rates for DHAV-3, DTMUV and NDRV were 13.33%, 10.37% and 8.15%, respectively. Using virus isolation as a reference, the triplex qPCR assay showed 100% detection sensitivity for all three viruses, with specificity and coincidence values above 97%. In conclusion, the established triplex TaqMan PCR is highly specific, sensitive and reproducible, providing a practical approach for detecting and monitoring DHAV-3, DTMUV and NDRV in ducks.
混合感染是一个严重问题,给养鸭业造成了巨大经济损失。鸭甲型肝炎病毒3型(DHAV-3)、鸭坦布苏病毒(DTMUV)和新型鸭呼肠孤病毒(NDRV)分别属于小RNA病毒科、黄病毒科和双链RNA病毒科,是感染鸭后具有相似症状的重要病原体。为了检测和区分这些病毒,本研究开发了一种三重实时荧光定量PCR检测方法,分别针对DHAV-3、DTMUV和NDRV的VP1、E和σC基因。在优化三重实时荧光定量PCR检测方法后进行了验证试验和临床应用。这种新型的三重检测方法显示出高特异性,与其他八种常见鸭病毒无交叉反应。DTMUV、DHAV-3和NDRV的检测限均为1×101拷贝/μL,批内和批间变异系数(CV)均低于4%。共检测了135份临床样本以评估该方法的可行性。DHAV-3、DTMUV和NDRV的阳性率分别为13.33%、10.37%和8.15%。以病毒分离为参照,三重荧光定量PCR检测方法对这三种病毒的检测灵敏度均为100%,特异性和符合率均高于97%。综上所述,所建立的三重TaqMan PCR具有高度特异性、敏感性和可重复性,为鸭群中DHAV-3、DTMUV和NDRV的检测和监测提供了一种实用方法。