Wang Xueyu, Xu Xin, Hu Wen, Zuo Kejing, Li Zhili, Kan Yunchao, Yao Lunguang, Ji Jun, Bi Yingzuo
Henan Provincial Engineering Laboratory of Insects Bio-reactor, China-UK-NYNU-RRes Joint Laboratory of Insect Biology, Nanyang Normal University, Wolong Road 1638, Nanyang, 473061, People's Republic of China.
Veterinary Laboratory, Guangzhou Zoo, Guangzhou, 510642, People's Republic of China.
BMC Vet Res. 2019 Apr 15;15(1):116. doi: 10.1186/s12917-019-1851-7.
Porcine epidemic diarrhea virus (PEDV) is a major etiological agent of porcine epidemic diarrhea around the world. Point-of-care testing in the field is lacking owing to the requirement for a simple, robust field applicable test that does not require professional laboratory equipment. The aim of this study was to establish a novel reverse transcription polymerase spiral reaction (RT-PSR) assay for the rapid detection of porcine epidemic diarrhea virus (PEDV). For the assay, a specific RT-PSR primer pair was designed against a conserved region in PEDV ORF3.
The RT-PSR was optimized, and PEDV could be detected after a 50 min incubation at 62 °C, in addition to the 15 min required for reverse transcription. No cross-reaction with other porcine infectious viruses was observed. This new method for PEDV detection was 10 times more sensitive than the conventional reverse transcription-polymerase chain reaction (RT-PCR) assay. The positive rates for 65 clinical samples using the new RT-PSR assay and the conventional RT-PCR assay were 58.46% (38/65) and 53.84% (35/65), respectively. In the RT-PSR assay, the addition of a mixture of dyes allowed a positive reaction to be directly observed by the naked eye.
These results indicate that this RT-PSR assay is capable of accurately detecting PEDV, and has the advantages of high specificity and sensitivity for the detection of PEDV.
猪流行性腹泻病毒(PEDV)是全球猪流行性腹泻的主要病原体。由于需要一种简单、可靠且无需专业实验室设备的现场适用检测方法,目前缺乏现场即时检测。本研究的目的是建立一种用于快速检测猪流行性腹泻病毒(PEDV)的新型逆转录聚合酶螺旋反应(RT-PSR)检测方法。针对该检测方法,针对PEDV ORF3中的保守区域设计了一对特异性RT-PSR引物。
对RT-PSR进行了优化,除逆转录所需的15分钟外,在62℃孵育50分钟后即可检测到PEDV。未观察到与其他猪传染性病毒的交叉反应。这种检测PEDV的新方法比传统逆转录聚合酶链反应(RT-PCR)检测方法灵敏10倍。使用新的RT-PSR检测方法和传统RT-PCR检测方法对65份临床样本的阳性率分别为58.46%(38/65)和53.84%(35/65)。在RT-PSR检测中,添加染料混合物后可直接用肉眼观察到阳性反应。
这些结果表明,这种RT-PSR检测方法能够准确检测PEDV,并且在检测PEDV方面具有高特异性和高灵敏度的优点。