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用于快速检测猪流行性腹泻病毒的逆转录交叉引物扩增-核酸检测试纸条

Reverse Transcription Cross-Priming Amplification-Nucleic Acid Test Strip for Rapid Detection of Porcine Epidemic Diarrhea Virus.

作者信息

Wang Feng-Xue, Yuan Dan-Yi, Jin Ya-Nan, Hu Lin, Sun Zhi-Yong, He Qian, Zhao Shi-Hua, Zhan Shu-Bai, Wen Yong-Jun

机构信息

State Key Laboratory of Special Economic Animal Molecular Biology, Institute of Special Economic Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, No. 4899 Juye Avenue, Jingyue Economic and Technological Development Zone, Changchun, Jilin, 130112, People's Republic of China.

(Sino-USA) SiChuan Nabii Bio-Tech Co., Ltd., Chengdu, SiChuan, 610041, People's Republic of China.

出版信息

Sci Rep. 2016 Apr 19;6:24702. doi: 10.1038/srep24702.

Abstract

Porcine epidemic diarrhea virus (PEDV) is a highly transmissible coronavirus that causes a severe enteric disease particularly in neonatal piglets. In this study, a rapid method for detecting PEDV was developed based on cross-priming amplification and nucleic acid test strip(CPA-NATS). Five primers specific for the N gene sequence of PEDV were used for the cross-priming amplification. Detection of amplification products based on labeled probe primers was conducted with strip binding antibody of labeled markers. The CPA method was evaluated and compared with a PCR method. The reverse transcription CPA system was further optimized for detecting PEDV RNA in clinical specimens. Results showed that the method was highly specific for the detection of PEDV, and had the same sensitivity as PCR, with detection limit of 10(-6) diluted plasmid containing the target gene of PEDV. It was also successfully applied to detecting PEDV in clinical specimens. The reverse transcription CPA-NATS detection system established in this study offers a specific, sensitive, rapid, and simple detection tool for screening PEDV, which can contribute to strategies in the effective control of PEDV in swine.

摘要

猪流行性腹泻病毒(PEDV)是一种高度传染性的冠状病毒,可引起严重的肠道疾病,尤其是在新生仔猪中。在本研究中,基于交叉引物扩增和核酸试纸条(CPA-NATS)开发了一种快速检测PEDV的方法。使用五条针对PEDV N基因序列的特异性引物进行交叉引物扩增。基于标记探针引物对扩增产物进行检测,使用标记物的试纸条结合抗体进行检测。对CPA方法进行了评估,并与PCR方法进行了比较。进一步优化了逆转录CPA系统,用于检测临床样本中的PEDV RNA。结果表明,该方法对PEDV的检测具有高度特异性,与PCR具有相同的灵敏度,检测限为含有PEDV靶基因的10^(-6)稀释质粒。该方法也成功应用于临床样本中PEDV的检测。本研究建立的逆转录CPA-NATS检测系统为PEDV的筛查提供了一种特异性强、灵敏度高、快速且简便的检测工具,有助于有效控制猪群中PEDV的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b849/4835727/338bace96931/srep24702-f1.jpg

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