Triplex fluorescence quantitative PCR detects duck hepatitis A virus type 3, Tembusu virus and novel reovirus.

IF 0.7 4区 农林科学 Q3 VETERINARY SCIENCES
Zhi Wu, Shuang Wu, Jun Xie, Huipeng Lu, Yong Jiang, Mengzhou Lin, Chenyi Gu, Shanyuan Zhu
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引用次数: 0

Abstract

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.

三重荧光定量PCR检测鸭甲型肝炎病毒3型、坦布苏病毒和新型呼肠孤病毒。
混合感染是造成鸭业重大经济损失的一个严重问题。鸭甲型肝炎病毒血清3型(DHAV-3)、鸭坦布舒病毒(DTMUV)和鸭新型呼肠孤病毒(NDRV)分别属于小核糖核酸病毒科、黄病毒科和spinareovirus科,是感染鸭后症状相似的重要病原体。为了检测和区分这些病毒,本研究建立了针对DHAV-3、DTMUV和NDRV的VP1、E和σC基因的三重实时PCR检测方法。验证试验和临床应用遵循优化的三重实时PCR法。该方法特异性高,与其他8种常见鸭病毒无交叉反应。DTMUV、DHAV-3和NDRV的检出限均为1 × 101拷贝/μL,试验内和试验间变异系数(CV)均小于4%。共对135个临床样本进行了测试,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qPCR检测方法对三种病毒的检测灵敏度均为100%,特异性和符合值均在97%以上。综上所述,所建立的TaqMan三重PCR具有高度的特异性、敏感性和重复性,为鸭DHAV-3、DTMUV和NDRV的检测和监测提供了一种实用的方法。
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来源期刊
Acta veterinaria Hungarica
Acta veterinaria Hungarica 农林科学-兽医学
CiteScore
1.80
自引率
0.00%
发文量
39
审稿时长
>36 weeks
期刊介绍: Acta Veterinaria Hungarica publishes original research papers presenting new scientific results of international interest, and to a limited extent also review articles and clinical case reports, on veterinary physiology (physiological chemistry and metabolism), veterinary microbiology (bacteriology, virology, immunology, molecular biology), on the infectious diseases of domestic animals, on veterinary parasitology, pathology, clinical veterinary science and reproduction.
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