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H9亚型禽流感病毒实时荧光重组酶聚合酶扩增检测方法的建立与应用

Development and application of a real-time fluorescent RAA assay for H9 subtype avian influenza viruses.

作者信息

Zhou Wanting, Li Xiaoqi, Tian Jie, Liu Shuo, Peng Cheng, Li Jinping, Hou Guangyu, Yang Jizhe, Jiang Wenming, Liu Hualei

机构信息

China Animal Health and Epidemiology Center, Qingdao, China.

College of Animal Science and Technology & College of Veterinary Medicine, Zhejiang Agriculture and Forestry University, Hangzhou, China.

出版信息

Virus Genes. 2025 Jun 11. doi: 10.1007/s11262-025-02167-x.

Abstract

The H9N2 subtype of avian influenza virus (AIV) is a critical pathogen responsible for avian infectious diseases, inducing respiratory symptoms in poultry and exhibiting high susceptibility to coinfections, which complicates clinical diagnosis. In this study, we designed specific primers and probes targeting the hemagglutinin (HA) gene of H9N2 AIV and developed a real-time fluorescent reverse transcription recombinase-aided isothermal amplification (RT-RAA) assay through systematic optimization of reaction components and conditions. The established method demonstrated exclusive reactivity with the H9N2 subtype, yielding negative results for all other tested viral pathogens, thereby showcasing high specificity. Analytical sensitivity testing revealed the capability to detect as low as 13.5 copies/μL of H9N2 viral RNA, indicating superior sensitivity. To further validate the practical application of this method, a total of 48 clinical samples, comprising oropharyngeal and cloacal swabs, were tested using the developed RT-RAA assay. The results revealed a positivity rate of 79%, reflecting strong diagnostic performance. This study presents a rapid RT-RAA assay characterized by high specificity and sensitivity, offering a robust technical platform for the immediate identification of H9N2 AIV and facilitating epidemiological surveillance in avian populations.

摘要

H9N2亚型禽流感病毒(AIV)是引起禽类传染病的关键病原体,可导致家禽出现呼吸道症状,并对合并感染表现出高度易感性,这使得临床诊断变得复杂。在本研究中,我们设计了针对H9N2 AIV血凝素(HA)基因的特异性引物和探针,并通过对反应成分和条件进行系统优化,开发了一种实时荧光逆转录重组酶辅助等温扩增(RT-RAA)检测方法。所建立的方法对H9N2亚型具有独特的反应性,对所有其他测试的病毒病原体均产生阴性结果,从而显示出高特异性。分析灵敏度测试表明,该方法能够检测低至13.5拷贝/μL的H9N2病毒RNA,表明其具有卓越的灵敏度。为了进一步验证该方法的实际应用,我们使用所开发的RT-RAA检测方法对总共48份临床样本(包括口咽拭子和泄殖腔拭子)进行了检测。结果显示阳性率为79%,反映出强大的诊断性能。本研究提出了一种具有高特异性和灵敏度的快速RT-RAA检测方法,为即时鉴定H9N2 AIV提供了一个强大的技术平台,并有助于禽类群体的流行病学监测。

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