Chen Qiu-Yong, Sun Zhi-Hua, Chen Ru-Jing, Wu Xue-Min, Che Yong-Liang, Wu Ren-Jie, Qiu Jing-Li, He Bing, Wang Long-Bai, Zhou Lun-Jiang
Institute of Animal Husbandry and Veterinary Medicine, Fujian Academy of Agriculture Sciences, Fuzhou, 350013, China.
Fujian Animal Disease Control Technology Development Center, Fuzhou, 350013, China.
BMC Vet Res. 2024 Dec 30;20(1):588. doi: 10.1186/s12917-024-04442-9.
Porcine teschovirus (PTV) is an important enteropathogen, associated with symptoms of polioencephalomyelitis, pneumonia, pericarditis, myocarditis, diarrhea, and reproductive disorders in pigs. Rapid and precise diagnostic methods are essential for managing PTV infections. The study introduced a simple, quick, and visual approach for detecting PTV through the use of RT-RAA coupled with LFD.
The procedures of RT-RAA-LFD for PTV could be carried out with 1.0 μmol/L primer concentration and 2.0 μmol/L probe concentration at 37 °C for 20 min, and the amplification result could be visualized within 5 min through LFD detection. Meanwhile, the assay established in this study showed no interaction with other associated diarrhea viruses, and has high specificity to PTV, with a minimal detection limit of 10 copies/μL and good repeatability. 128 clinical samples suspected of having a PTV infection were tested by RT-PCR and RT-RAA-LFD, respectively. The total diagnostic coincidence rate was 98.44% (126/128) with a Kappa value of 0.96(K ≥ 0.75), demonstrating a high degree of agreement to detect PTV for the two methods.
The RT-RAA-LFD assay created in this research displayed quick response, specificity, and sensitivity, capable of successfully detecting PTV in less than 25 min, providing an easy-to-use diagnostic instrument for rapid and visual PTV detection, especially suitable for labs and low-resource environments.
猪捷申病毒(PTV)是一种重要的肠道病原体,与猪的脑脊髓灰质炎、肺炎、心包炎、心肌炎、腹泻及繁殖障碍症状有关。快速准确的诊断方法对于管理PTV感染至关重要。本研究介绍了一种通过逆转录-重组酶介导的等温扩增(RT-RAA)结合侧向流动免疫分析(LFD)来检测PTV的简单、快速且可视化的方法。
PTV的RT-RAA-LFD检测程序在引物浓度为1.0 μmol/L、探针浓度为2.0 μmol/L、37℃条件下进行20分钟,扩增结果可通过LFD检测在5分钟内可视化。同时,本研究建立的检测方法与其他相关腹泻病毒无交叉反应,对PTV具有高度特异性,最低检测限为10拷贝/μL,重复性良好。分别用RT-PCR和RT-RAA-LFD检测了128份疑似PTV感染的临床样本。总诊断符合率为98.44%(126/128),Kappa值为0.96(K≥0.75),表明两种方法检测PTV的一致性程度很高。
本研究建立的RT-RAA-LFD检测方法具有快速响应、特异性和敏感性,能够在不到25分钟的时间内成功检测PTV,为PTV的快速可视化检测提供了一种易于使用的诊断工具,特别适用于实验室和资源匮乏的环境。