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一种用于同时检测新型鹅细小病毒和新型鸭呼肠孤病毒的TaqMan一步法定量PCR检测方法的开发。

Development of a TaqMan One-Step Quantitative PCR Assay for the Simultaneous Detection of Novel Goose Parvovirus and Novel Duck Reovirus.

作者信息

Wang Yimin, Wang Yong, Bi Zhuangli, Wang Jinbin, Wang Gang, Ru Xin, Meng Chunchun, Zhu Jie, Liu Guangqing, Li Chuanfeng

机构信息

Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences (CAAS), Shanghai 200241, China.

College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China.

出版信息

Microorganisms. 2025 Jul 4;13(7):1582. doi: 10.3390/microorganisms13071582.

Abstract

The novel goose parvovirus (NGPV) and the novel duck reovirus (NDRV) are pathogens that can substantially affect the growth and development of ducklings, causing considerable economic losses to duck farms. Therefore, a timely, rapid, accurate, and high-throughput diagnosis and identification of viral infections are critical for preventing the spread of epidemics. In this study, a TaqMan probe-based duplex one-step RT-qPCR was established for the simultaneous detection and qualitative and quantitative identification of the two viruses. It demonstrated greater sensitivity than conventional PCR, detecting as low as 2.42 copies/μL of NGPV genome and 70.1 copies/μL of NDRV genome. Additionally, it exhibited remarkable specificity, responding exclusively to the nucleic acids of target pathogens. It also demonstrated excellent reproducibility and availability, particularly in clinical settings, with a coinfection detection rate of 13.3%, contributing to the development of NGPV- and NDRV-testing technologies.

摘要

新型鹅细小病毒(NGPV)和新型鸭呼肠孤病毒(NDRV)是可严重影响雏鸭生长发育的病原体,给鸭场造成相当大的经济损失。因此,及时、快速、准确且高通量地诊断和鉴定病毒感染对于预防疫情传播至关重要。在本研究中,建立了一种基于TaqMan探针的双重一步法RT-qPCR,用于同时检测这两种病毒并进行定性和定量鉴定。它显示出比传统PCR更高的灵敏度,可检测低至2.42拷贝/μL的NGPV基因组和70.1拷贝/μL的NDRV基因组。此外,它具有显著的特异性,仅对目标病原体的核酸有反应。它还表现出出色的重复性和实用性,特别是在临床环境中,共感染检测率为13.3%,有助于NGPV和NDRV检测技术的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5010/12299775/19f01b75b640/microorganisms-13-01582-g001.jpg

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