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开发并验证一种通用的一步法 RT-PCR 检测方法,用于广泛检测鸭坦布苏病毒。

Development and Validation of a Universal One-Step RT-PCR Assay for Broad Detection of Duck Tembusu Virus.

机构信息

Department of Veterinary Microbiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand, 10330.

Emerging and Re-emerging Infectious Diseases in Animals (CUEIDAs), Center of Excellence, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand, 10330.

出版信息

Avian Dis. 2020 Sep 1;64(3):294-299. doi: 10.1637/aviandiseases-D-19-00199.

Abstract

Duck Tembusu virus (DTMUV), a mosquito-borne flavivirus, has been identified as a causative agent of an emerging disease in ducks. Since its first report in 2010, several clusters of DTMUV have increasingly been identified and caused outbreaks in many Asian countries. This highlights the need for improved and novel broad detection assays in order to detect all circulating clusters of DTMUV. In this study, a universal one-step reverse-transcription PCR (RT-PCR) assay targeting a highly conserved region of the NS5 gene was developed and validated for broad detection of all DTMUV clusters. The newly developed universal RT-PCR assay could specifically detect all clusters of DTMUV without cross-reactions with common duck viruses and other related flaviviruses. The assay was able to detect DTMUV as low as a 0.001 50% embryo lethal dose/milliliter. The performance of the assay was evaluated by using experimental and field clinical samples. The assay could successfully detect DTMUV in all experimentally DTMUV-infected samples and gave a higher DTMUV detection rate (36%) than the previously reported envelope-specific RT-PCR assay (30%) in field clinical samples. All the positive samples were confirmed DTMUV-positive by DNA sequencing. In conclusion, the newly developed universal RT-PCR assay exhibited high accuracy, specificity, and sensitivity in broad DTMUV detection, thus providing an improved screening assay for routine detection and epidemiologic surveillance of DTMUV.

摘要

鸭坦布苏病毒(DTMUV)是一种蚊媒黄病毒,已被确定为一种新兴鸭病的病原体。自 2010 年首次报告以来,越来越多的 DTMUV 聚集被识别出来,并在许多亚洲国家引发了疫情。这凸显了需要改进和新型的广泛检测方法,以便检测所有循环的 DTMUV 聚集。在这项研究中,开发并验证了一种针对 NS5 基因高度保守区域的通用一步逆转录 PCR(RT-PCR)检测方法,用于广泛检测所有 DTMUV 聚集。新开发的通用 RT-PCR 检测方法能够特异性地检测所有 DTMUV 聚集,而与常见鸭病毒和其他相关黄病毒无交叉反应。该检测方法能够检测到低至 0.00150%的半数胚胎致死剂量/毫升的 DTMUV。通过使用实验和现场临床样本评估了该检测方法的性能。该检测方法能够成功地检测到所有实验感染 DTMUV 的样本中的 DTMUV,并且在现场临床样本中的 DTMUV 检测率(36%)高于先前报道的包膜特异性 RT-PCR 检测方法(30%)。所有阳性样本均通过 DNA 测序确认 DTMUV 阳性。总之,新开发的通用 RT-PCR 检测方法在广泛的 DTMUV 检测中表现出了高准确性、特异性和敏感性,从而为 DTMUV 的常规检测和流行病学监测提供了一种改进的筛选检测方法。

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