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Equipment-free recombinase polymerase amplification assay using body heat for visual and rapid point-of-need detection of canine parvovirus 2

机译:使用体热的无设备重组酶聚合酶扩增试验可用于视觉和快速检测犬细小病毒2

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摘要

A visible and equipment-free recombinase polymerase amplification assay combined with a lateral flow strip (LFS RPA) was developed to detect canine parvovirus type 2 (CPV-2), which is the etiological agent of canine parvovirus disease. The CPV-2 LFS RPA assay was developed based on the VP2 gene and is performed in a closed fist using body heat for 15 min; the products are visible to the naked eye on the LFS within 5 min. The assay could detect CPV-2a, CPV-2b and CPV-2c, and there was no cross-reaction with the other viruses tested. Using the standard CPV-2 DNA as a template, the analytical sensitivity was 1.0 × 10 copies per reaction, which was the same result as that of a real-time PCR. The assay performance was further evaluated by testing 60 canine fecal samples, and CPV-2 DNA was detected in 46 samples (76.7%, 46/60) by LFS RPA, which was the same result as that of the real-time PCR assay and higher than that of the SNAP method (48.3%, 29/60). The novel CPV-2 LFS RPA assay is an attractive and promising tool for rapid and convenient diagnosis of CPV disease, especially cage side and in underequipped laboratories.
机译:开发了一种可视且无需设备的重组酶聚合酶扩增试验,并结合了侧向流条(LFS RPA)来检测2型犬细小病毒(CPV-2),这是犬细小病毒病的病原体。 CPV-2 LFS RPA分析是基于VP2基因开发的,在封闭的拳头中使用人体热量进行15分钟。在5分钟内,肉眼即可在LFS上看到产品。该测定法可以检测到CPV-2a,CPV-2b和CPV-2c,并且与其他测试病毒没有交叉反应。以标准的CPV-2 DNA为模板,每个反应的分析灵敏度为1.0××10拷贝,与实时PCR的结果相同。通过测试60个犬粪便样品进一步评估了测定性能,通过LFS RPA在46个样品中检出了CPV-2 DNA(76.7%,46/60),其结果与实时PCR测定和高于SNAP方法(48.3%,29/60)。新颖的CPV-2 LFS RPA测定法是快速,方便地诊断CPV疾病(尤其是笼侧和设备不足的实验室)的一种有吸引力且有前途的工具。

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