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用于快速检测口蹄疫病毒的无视觉和设备的逆转录重组酶聚合酶扩增方法

Visual and equipment-free reverse transcription recombinase polymerase amplification method for rapid detection of foot-and-mouth disease virus.

作者信息

Liu Libing, Wang Jinfeng, Zhang Ruoxi, Lin Mi, Shi Ruihan, Han Qingan, Wang Jianchang, Yuan Wanzhe

机构信息

Center of Inspection and Quarantine, Hebei Entry-Exit Inspection and Quarantine Bureau, Shijiazhuang, 050051, People's Republic of China.

Hebei Animal Disease Control Center, Shijiazhuang, 050050, People's Republic of China.

出版信息

BMC Vet Res. 2018 Aug 31;14(1):263. doi: 10.1186/s12917-018-1594-x.

Abstract

BACKGROUND

Foot-and-mouth disease (FMD), which is caused by foot-and-mouth disease virus (FMDV), is a highly contagious tansboundary disease of cloven-hoofed animals and causes devastating economic damages. Accurate, rapid and simple detection of FMDV is critical to containing an FMD outbreak. Recombinase polymerase amplification (RPA) has been explored for detection of diverse pathogens because of its accuracy, rapidness and simplicity. A visible and equipment-free reverse-transcription recombinase polymerase amplification assay combined with lateral flow strip (LFS RT-RPA) was developed to detect the FMDV using primers and LF probe specific for the 3D gene.

RESULTS

The FMDV LFS RT-RPA assay was performed successfully in a closed fist using body heat for 15 min, and the products were visible on the LFS inspected by the naked eyes within 2 min. The assay could detect FMDV serotypes O, A and Asia1, and there were no cross-reactions with vesicular stomatitis virus (VSV), encephalomyocarditis virus (EMCV), classical swine fever virus (CSFV), porcine reproductive and respiratory syndrome virus (PRRSV), porcine circovirus 2 (PCV2) and pseudorabies virus (PRV). The analytical sensitivity was 1.0 × 10 copies in vitro transcribed FMDV RNA per reaction, which was the same as a real-time RT-PCR. For the 55 samples, FMDV RNA positive rate was 45.5% (25/55) by LFS RT-RPA and 52.7% (29/55) by real-time RT-PCR. For the LFS RT-RPA assay, the positive and negative predicative values were 100% and 80%, respectively.

CONCLUSIONS

The performance of the LFS RT-RPA assay was comparable to real-time RT-PCR, while the LFS RT-RPA assay was much faster and easier to be performed. The developed FMDV LFS RT-RPA assay provides an attractive and promising tool for rapid and reliable detection of FMDV in under-equipped laboratory and at point-of-need facility, which is of great significance in FMD control in low resource settings.

摘要

背景

口蹄疫(FMD)由口蹄疫病毒(FMDV)引起,是偶蹄动物的一种高度传染性跨界疾病,会造成毁灭性的经济损失。准确、快速且简便地检测FMDV对于控制口蹄疫疫情至关重要。重组酶聚合酶扩增技术(RPA)因其准确性、快速性和简便性,已被用于多种病原体的检测。本研究开发了一种结合侧向流动试纸条(LFS)的可视化且无需仪器的逆转录重组酶聚合酶扩增检测方法(LFS RT-RPA),使用针对3D基因的引物和LF探针来检测FMDV。

结果

FMDV LFS RT-RPA检测方法在握拳状态下利用体温成功进行了15分钟,产物在2分钟内即可通过肉眼在LFS试纸上观察到。该检测方法能够检测口蹄疫病毒O型、A型和亚洲1型,与水疱性口炎病毒(VSV)、脑心肌炎病毒(EMCV)、经典猪瘟病毒(CSFV)、猪繁殖与呼吸综合征病毒(PRRSV)、猪圆环病毒2型(PCV2)和伪狂犬病病毒(PRV)无交叉反应。其体外转录的FMDV RNA的分析灵敏度为每个反应1.0×10拷贝,与实时RT-PCR相同。对于55份样本,LFS RT-RPA检测的FMDV RNA阳性率为45.5%(25/55),实时RT-PCR检测的阳性率为52.7%(29/55)。对于LFS RT-RPA检测方法,阳性预测值和阴性预测值分别为100%和80%。

结论

LFS RT-RPA检测方法的性能与实时RT-PCR相当,但其速度更快且操作更简便。所开发的FMDV LFS RT-RPA检测方法为在设备简陋的实验室和现场需求点快速可靠地检测FMDV提供了一种有吸引力且有前景的工具,这对于资源匮乏地区的口蹄疫防控具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d0e/6119248/0e6ca411ac1d/12917_2018_1594_Fig1_HTML.jpg

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