Suppr超能文献

基于SYBR Green I的低价双重定量PCR检测方法的开发与应用,用于同时检测猪德尔塔冠状病毒和猪萨佩罗病毒。

Development and application of a low-priced duplex quantitative PCR assay based on SYBR Green I for the simultaneous detection of porcine deltacoronavirus and porcine sapelovirus.

作者信息

Lu Si-Jia, Ma Meng-Yao, Yan Xiao-Guang, Zhao Fu-Jie, Hu Wen-Yang, Ding Qing-Wen, Ren Hao-Jie, Xiang Yu-Qiang, Zheng Lan-Lan

机构信息

College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, Henan, P.R. China.

出版信息

Vet Med (Praha). 2023 Mar 23;68(3):106-115. doi: 10.17221/79/2022-VETMED. eCollection 2023 Mar.

Abstract

Porcine deltacoronavirus (PDCoV) and porcine sapelovirus (PSV) are two viruses that can cause diarrhoea in pigs and bring great economic loss to the pig industry. In this research, a duplex real-time quantitative polymerase chain reaction (qPCR) assay based on SYBR Green I was developed to simultaneously detect PDCoV and PSV. No specific melting peaks were found in other porcine diarrhoea-associated viruses, indicating that the method developed in this study had good specificity. The detection limits of PDCoV and PSV were 1.0 × 10 copies μl and 1.0 × 10 copies μl, respectively. The duplex real-time qPCR assay tested two hundred and three (203) intestinal and faecal samples collected from diarrhoeal and asymptomatic pigs. The positive rates of PDCoV and PSV were 20.2% and 23.2%, respectively. The co-infection rate of PDCoV and PSV was 13.8%. To evaluate the accuracy of the developed method, conventional PCR and singular TaqMan real-time qPCR assays for PDCoV/PSV were also used to detect the samples. The results showed that the duplex real-time qPCR assay was consistent with the singular assays, but its sensitivity was higher than conventional PCR methods. This duplex real-time qPCR assay provides a rapid, sensitive and reliable method in a clinic to simultaneously detect PDCoV and PSV.

摘要

猪德尔塔冠状病毒(PDCoV)和猪萨佩罗病毒(PSV)是两种可导致猪腹泻并给养猪业带来巨大经济损失的病毒。在本研究中,开发了一种基于SYBR Green I的双重实时定量聚合酶链反应(qPCR)检测方法,用于同时检测PDCoV和PSV。在其他猪腹泻相关病毒中未发现特异性熔解峰,表明本研究开发的方法具有良好的特异性。PDCoV和PSV的检测限分别为1.0×10拷贝/μl和1.0×10拷贝/μl。该双重实时qPCR检测方法对从腹泻和无症状猪采集的203份肠道和粪便样本进行了检测。PDCoV和PSV的阳性率分别为20.2%和23.2%。PDCoV和PSV的共感染率为13.8%。为评估所开发方法的准确性,还使用了针对PDCoV/PSV的常规PCR和单重TaqMan实时qPCR检测方法对样本进行检测。结果表明,双重实时qPCR检测方法与单重检测方法结果一致,但其灵敏度高于常规PCR方法。这种双重实时qPCR检测方法为临床同时检测PDCoV和PSV提供了一种快速、灵敏且可靠的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a16/10581527/2256fea0f4fc/VETMED-68-122079-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验