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建立一种通过磁微球和纳米颗粒结合双检测同时检测猪流行性腹泻病毒和传染性胃肠炎病毒的方法。

Establishment of method for dual simultaneous detection of PEDV and TGEV by combination of magnetic micro-particles and nanoparticles.

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, PR China.

College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, PR China.

出版信息

J Infect Chemother. 2020 May;26(5):523-526. doi: 10.1016/j.jiac.2020.01.008. Epub 2020 Mar 5.

Abstract

Transmissible gastroenteritis virus (TGEV) and porcine epidemic diarrhea virus (PEDV) are the main pathogens causing viral diarrhea in pig, mixed infections of these two viruses are very common in intensive pig rearing. However, there is a lack of a method to simultaneously detect and distinguish PEDV and TGEV in preclinical levels. In this study, we aimed to establish a dual ultrasensitive nanoparticle DNA probe-based PCR assay (dual UNDP-PCR) based on functionalized magnetic bead enrichment and specific nano-technology amplification for simultaneous detection and distinguish diagnosis of PEDV and TGEV. The detection limit of dual UNDP-PCR for single or multiple infections of PEDV and TGEV is 25 copies/g, which is 400 times more sensitive than the currently known duplex RT-PCR, showing better specificity and sensitivity without cross-reaction with other viruses. For pre-clinical fecal samples, the dual UNDP-PCR showed a markedly higher positive detection rate (52.08%) than conventional duplex RT-PCR (13.21%), can rapidly and accurately identify targeted pathogens whenever simple virus infection or co-infection. In summary, this study provides a technique for detecting and distinguishing PEDV and TGEV in preclinical levels, which is high sensitivity, specificity, repeatability, low cost and broad application prospect.

摘要

传染性胃肠炎病毒(TGEV)和猪流行性腹泻病毒(PEDV)是引起猪病毒性腹泻的主要病原体,这两种病毒在集约化养猪场混合感染非常普遍。然而,目前缺乏一种方法能够在临床前水平同时检测和区分 PEDV 和 TGEV。本研究旨在建立一种基于功能化磁珠富集和特定纳米技术扩增的双重超敏纳米颗粒 DNA 探针 PCR 检测方法(dual UNDP-PCR),用于同时检测和区分 PEDV 和 TGEV。dual UNDP-PCR 对 PEDV 和 TGEV 单一或混合感染的检测限为 25 拷贝/g,比目前已知的双重 RT-PCR 灵敏 400 倍,具有更好的特异性和敏感性,与其他病毒无交叉反应。对于临床前粪便样本,dual UNDP-PCR 的阳性检出率(52.08%)明显高于传统的双重 RT-PCR(13.21%),无论简单病毒感染还是混合感染,均可快速准确地识别目标病原体。综上所述,本研究提供了一种用于临床前水平检测和区分 PEDV 和 TGEV 的技术,该技术具有高灵敏度、特异性、重复性、低成本和广泛的应用前景。

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