利用基于 Taqman 探针的多重实时 PCR 快速诊断犬呼吸道冠状病毒、犬流感病毒、犬瘟热病毒和犬副流感病毒。

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2024-05-31 DOI:10.1016/j.jviromet.2024.114960
Hu Zhou , Haoqi Li , Xuehan Sun , Jiaqi Lin , Chengguang Zhang , Jianqing Zhao , Ling Zhao , Ming Zhou
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引用次数: 0

摘要

犬传染性呼吸道疾病综合症(CIRDC)是一种高度传染性疾病。犬呼吸道冠状病毒 (CRCoV)、犬流感病毒 (CIV)、犬瘟热病毒 (CDV) 和犬副流感病毒 (CPiV) 是导致 CIRDC 的主要病原体。由于这些病毒诱发的临床症状相似,因此仅根据症状进行鉴别诊断具有挑战性。本研究开发了一种多重实时 PCR 检测方法,用于检测 CIRDC 的四种 RNA 病毒。针对 CRCoV 的 M 基因、CIV 的 M 基因、CDV 的 N 基因和 CPiV 的 NP 基因设计了特定的引物和探针。CIV 或 CRCoV 的检测限为每微升 10 个拷贝,而 CDV 或 CPiV 的检测限为每微升 100 个拷贝。组内和组间重复性变异系数(CV)均小于 2%。本研究共分析了 341 份临床犬样本,结果表明,与传统的反转录 PCR 相比,本研究开发的方法具有良好的一致性和更高的特异性。本研究提供了一种新方法,可在一次反应中同时检测所有四种病原体,提高了监测四种病毒在犬瘟热流行情况的效率,有利于犬瘟热的控制。
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Rapid diagnosis of canine respiratory coronavirus, canine influenza virus, canine distemper virus and canine parainfluenza virus with a Taqman probe-based multiplex real-time PCR

Canine Infectious Respiratory Disease Complex (CIRDC) is a highly infectious diseases. Canine respiratory coronavirus (CRCoV), Canine influenza virus (CIV), Canine distemper virus (CDV), and Canine parainfluenza virus (CPiV) are crucial pathogens causing CIRDC. Due to the similar clinical symptoms induced by these viruses, differential diagnosis based solely on symptoms can be challenging. In this study, a multiplex real-time PCR assay was developed for detecting the four RNA viruses of CIRDC. Specific primers and probes were designed to target M gene of CRCoV, M gene of CIV, N gene of CDV and NP gene of CPiV. The detection limit is 10 copies/μL for CIV or CRCoV, while the detection limit of CDV or CPiV is 100 copies/μL. Intra-group and inter-group repeatability coefficient of variation (CV) were both less than 2 %. A total of 341 clinical canine samples were analyzed, and the results indicated that the method developed in our study owns a good consistency and better specificity compared with the conventional reverse transcription PCR. This study provides a new method to enable the simultaneous detection of all four pathogens in a single reaction, improving the efficiency for monitoring the prevalence of four viruses in CIRDC, which benefits the control of CIRDC.

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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
期刊最新文献
Performance evaluation of TaqMan™ Arbovirus Triplex Kit (ZIKV/DENV/CHIKV) for detection and differentiation of dengue and chikungunya viral RNA in serum samples of symptomatic patients. Climatic determinants of monkeypox transmission: A multi-national analysis using generalized count mixed models. Corrigendum to "Rapid detection of bat coronaviruses from fecal samples using loop-mediated isothermal amplification assay in the field" J. Virol. Methods 330 (December) (2024) 115035. Corrigendum to "Generation of infectious clone of bovine adenovirus type I expressing a visible marker gene" [J. Virol. Methods 261 (2018) 139-146]. Effect of Time and Temperature on the Stability of HPV and Cellular Nucleic Acid using Simulated Dry Self-Samples.
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