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用于快速灵敏检测口蹄疫病毒的现场可部署逆转录绝缘等温PCR(RT-iiPCR)检测法

Field-Deployable Reverse Transcription-Insulated Isothermal PCR (RT-iiPCR) Assay for Rapid and Sensitive Detection of Foot-and-Mouth Disease Virus.

作者信息

Ambagala A, Fisher M, Goolia M, Nfon C, Furukawa-Stoffer T, Ortega Polo R, Lung O

机构信息

Canadian Food Inspection Agency, National Centres for Animal Disease, Lethbridge Laboratory, Lethbridge, AB, Canada.

Canadian Food Inspection Agency, National Centre for Foreign Animal Diseases, Canadian Science Centre for Human and Animal Health, Winnipeg, MB, Canada.

出版信息

Transbound Emerg Dis. 2017 Oct;64(5):1610-1623. doi: 10.1111/tbed.12554. Epub 2016 Sep 3.

Abstract

Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals, which can decimate the livestock industry and economy of countries previously free of this disease. Rapid detection of foot-and-mouth disease virus (FMDV) is critical to containing an FMD outbreak. Availability of a rapid, highly sensitive and specific, yet simple and field-deployable assay would support local decision-making during an FMDV outbreak. Here we report validation of a novel reverse transcription-insulated isothermal PCR (RT-iiPCR) assay that can be performed on a commercially available, compact and portable POCKIT analyser that automatically analyses data and displays '+' or '-' results. The FMDV RT-iiPCR assay targets the 3D region of the FMDV genome and was capable of detecting 9 copies of in vitro-transcribed RNA standard with 95% confidence. It accurately identified 63 FMDV strains belonging to all seven serotypes and showed no cross-reactivity with viruses causing similar clinical diseases in cloven-hoofed animals. The assay was able to identify FMDV RNA in multiple sample types including oral, nasal and lesion swabs, epithelial tissue suspensions, vesicular and oral fluid samples, even before the appearance of clinical signs. Clinical sensitivity of the assay was comparable or slightly higher than the laboratory-based real-time RT-PCR assay in use. The assay was able to detect FMDV RNA in vesicular fluid samples without nucleic acid extraction. For RNA extraction from more complex sample types, a commercially available taco mini transportable magnetic bead-based, automated extraction system was used. This assay provides a potentially useful field-deployable diagnostic tool for rapid detection of FMDV in an outbreak in FMD-free countries or for routine diagnostics in endemic countries with less structured laboratory systems.

摘要

口蹄疫(FMD)是偶蹄类动物的一种高度传染性病毒性疾病,可使以前无此病的国家的畜牧业和经济遭受重创。快速检测口蹄疫病毒(FMDV)对于控制口蹄疫疫情至关重要。一种快速、高度灵敏且特异、同时又简单且可在现场部署的检测方法,将有助于在FMDV疫情期间进行本地决策。在此,我们报告了一种新型逆转录绝缘等温PCR(RT-iiPCR)检测方法的验证情况,该方法可在市售的紧凑型便携式POCKIT分析仪上进行,该分析仪能自动分析数据并显示“+”或“-”结果。FMDV RT-iiPCR检测方法靶向FMDV基因组的3D区域,能够以95%的置信度检测到9个体外转录RNA标准品拷贝。它准确鉴定了属于所有七个血清型的63种FMDV毒株,并且与在偶蹄类动物中引起类似临床疾病的病毒无交叉反应。该检测方法能够在多种样本类型中鉴定FMDV RNA,包括口腔、鼻腔和病变拭子、上皮组织悬液、水疱液和口腔液体样本,甚至在临床症状出现之前就能检测到。该检测方法的临床敏感性与正在使用的基于实验室的实时RT-PCR检测方法相当或略高。该检测方法无需核酸提取就能在水疱液样本中检测到FMDV RNA。对于从更复杂样本类型中提取RNA,使用了市售的基于塔可微型可移动磁珠的自动提取系统。该检测方法为在无口蹄疫国家的疫情中快速检测FMDV或在实验室系统结构较差的流行国家进行常规诊断提供了一种潜在有用的可在现场部署的诊断工具。

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