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用于检测鸭肠炎病毒、鹅细小病毒和番鸭细小病毒的多重定量聚合酶链反应检测方法的开发

Development of a Multiplex Quantitative Polymerase Chain Reaction Assay for the Detection of Duck Enteritis Virus, Goose Parvovirus, and Muscovy Duck Parvovirus.

作者信息

Qiu Qian, Hu Ruiming, Liu Zirui, Yan Linjie, Yang Fan, Dai Xueyan, Xing Chenghong, Cao Huabin

机构信息

Jiangxi Provincial Key Laboratory for Animal Health, Institute of Animal Population Health, College of Animal Science and Technology, Jiangxi Agricultural University, No. 1101 Zhimin Avenue, Economic and Technological Development District, Nanchang 330045, China.

Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, No. 22 Xinong Road, Yangling District, Xianyang 712000, China.

出版信息

Animals (Basel). 2025 May 29;15(11):1599. doi: 10.3390/ani15111599.

Abstract

Duck enteritis virus (DEV), goose parvovirus (GPV), and muscovy duck parvovirus (MDPV) all have similar symptoms after infection, such as severe diarrhea, which seriously affects the healthy development of the waterfowl industry. Hence, it is important to devise a rapid and precise assay for the detection of these three viruses. In this study, a TaqMan probe-based multi-quantitative polymerase chain reaction (qPCR) assay was developed and optimized. Three specific primers and probes were designed according to the conserved regions of UL6 of DEV, REP of GPV, and VP1 of MDPV, respectively. DEV demonstrated a detection limit of 11.6 copies, GPV detected a limit of 95 copies, and MDPV showcased a detection limit of 14.8 copies. The correlation coefficient is greater than 0.99, and the amplification efficiency is 89% to 93%. These results indicate that the multiplex qPCR assay has high sensitivity, specificity, and stability. Of the 215 clinical samples used in this study, 33 tested DEV positive, 25 tested GPV positive, and 24 tested MDPV positive. Overall, the assay established in the current study presents a rapid, efficient, specific, and sensitive tool for of detecting DEV, GPV, and MDPV.

摘要

鸭肠炎病毒(DEV)、鹅细小病毒(GPV)和番鸭细小病毒(MDPV)感染后均有相似症状,如严重腹泻,这严重影响水禽产业的健康发展。因此,设计一种快速、精确的检测这三种病毒的方法很重要。在本研究中,开发并优化了一种基于TaqMan探针的多重定量聚合酶链反应(qPCR)检测方法。根据DEV的UL6、GPV的REP和MDPV的VP1保守区域分别设计了三条特异性引物和探针。DEV的检测限为11.6拷贝,GPV的检测限为95拷贝,MDPV的检测限为14.8拷贝。相关系数大于0.99,扩增效率为89%至93%。这些结果表明多重qPCR检测方法具有高灵敏度、特异性和稳定性。在本研究使用的215份临床样本中,33份DEV检测呈阳性,25份GPV检测呈阳性,24份MDPV检测呈阳性。总体而言,本研究建立的检测方法为检测DEV、GPV和MDPV提供了一种快速、高效、特异且灵敏的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1c8/12153826/d5ac4793aafa/animals-15-01599-g001.jpg

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