基于 TaqMan 探针的一步法多重实时 RT-PCR 分析法用于口蹄疫诊断

J. Biswal, J. Mohapatra, Rajeev Ranjan, M. Rout, Shyam Singh Dahiya, Rabindra Prasad Singh
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引用次数: 0

摘要

有效控制和监测口蹄疫(FMD)的传播有赖于实验室对口蹄疫病毒(FMDV)快速准确的检测。因此,本报告开发并评估了一种基于 TaqMan 探针的多重一步式 RT-qPCR 检测方法,该方法在单个反应管中同时检测 FMDV 5′UTR 和 3Dpol 区域以及 18S rRNA 家系基因(作为内部对照)。该多重一步式 RT-qPCR 检测法可特异性检测感染 FMDV 的细胞培养悬液和从已知感染 FMD 的动物身上采集的临床样本中的病毒基因组。该检测方法可检测过去二十年间在印度收集的存档 FMDV 细胞培养分离物(n = 120)中的 FMDV RNA。此外,新测定法还能检测从各种现场疫情中收集的疑似口蹄疫临床样本(n = 740)中的病毒 RNA。在临界 Ct 值小于 38 时,该检测方法可分别检测出至少 20 和 10 个 FMDV 3Dpol 和 5′UTR 基因拷贝。此外,多重 RT-qPCR 检测证明是稳健的,FMDV-3Dpol 基因目标检测的检测间变异系数为 1.3% 至 3.03%,5′UTR 基因目标检测的检测间变异系数为 1.44% 至 4.69%。此外,研究还发现,新检测方法可用于检测多种样本(上皮细胞、唾液、OPF、牛奶和血液)中的病毒基因组,且检测限没有显著差异。因此,多重一步式 RT-qPCR 检测法可被视为印度检测口蹄疫病毒的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TaqMan probe-based one-step multiplex real-time RT-PCR assay for the diagnosis of foot-and-mouth disease
Effective control and monitoring the spread of foot-and-mouth disease (FMD) relies upon rapid and accurate laboratory detection of FMD virus (FMDV). Therefore, in this report, a multiplex TaqMan probe-based one-step RT-qPCR assay simultaneously targeting FMDV 5′UTR and 3Dpol regions, and 18S rRNA housekeeping gene (as an internal control) in a single reaction tube was developed and evaluated. The multiplex one-step RT-qPCR assay specifically detected viral genome in both FMDV-infected cell culture suspensions and clinical samples collected from known-FMD infected animals. The assay could detect FMDV RNA in the archived FMDV cell culture isolates (n = 120) collected during the last two decades in India. In addition, the new assay could also detect viral RNA in the FMD suspected clinical samples (n = 740) collected from various field outbreaks. At a cut-off Ct-value of <38, the assay could detect at least 20 and 10 copies of FMDV 3Dpol and 5′UTR genes, respectively. Further, the multiplex RT-qPCR assay proved to be robust, showing an inter-assay co-efficient of variations ranging from 1.3% to 3.03% for FMDV-3Dpol gene target, and from 1.44% to 4.69% for 5′UTR gene target. In addition, it was found that the new assay could be used to detect viral genome in a variety of samples (epithelium, saliva, OPF, milk and blood) without any significance difference in the detection limit of the assay. Hence, the multiplex one-step RT-qPCR assay could be considered a valuable tool for the detection of FMDV in India.
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