犬冠状病毒、犬呼吸道冠状病毒、犬腺病毒2型和犬诺如病毒四重RT-qPCR检测方法的建立

IF 3.3 3区 医学 Q2 MICROBIOLOGY Pathogens Pub Date : 2024-11-29 DOI:10.3390/pathogens13121054
Kaichuang Shi, Yandi Shi, Yuwen Shi, Feng Long, Yanwen Yin, Yi Pan, Zongqiang Li, Shuping Feng
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引用次数: 0

摘要

犬冠状病毒(CCoV)、犬呼吸道冠状病毒(CRCoV)、犬腺病毒2型(CAV-2)和犬诺如病毒(CNV)是犬病毒性胃肠道和呼吸道疾病的重要病原体。特别是,与这些病毒的共同感染加剧了疾病的损害。本研究设计了四对引物和探针特异性扩增CCoV M基因、CRCoV N基因、CAV-2六邻体基因和CNV RdRp基因的保守区域。优化不同的反应条件,建立检测CCoV、CRCoV、CAV-2和CNV的四重RT-qPCR。对所建立的检测方法的特异性、敏感性和可重复性进行了评价。然后,利用该方法对2022-2024年广西宠物医院的1688份临床样本进行检测,验证其临床适用性。此外,还使用报告的参考RT-qPCR检测方法对这些样品进行了评估,并确定了开发的检测方法与参考检测方法之间的一致性。结果表明,该四重RT-qPCR仅能特异性检测CCoV、CRCoV、CAV-2和CNV,与其他犬病毒无交叉反应。该方法对CCoV、CRCoV、CAV-2和CNV的检测限(lod)为1.0 × 102拷贝/反应,灵敏度高。重复性好,组内变异性为0.19 ~ 1.31%,组间变异性为0.10 ~ 0.88%。采用该方法检测CCoV、CRCoV、CAV-2和CNV的阳性率分别为8.59%(145/1688)、8.65%(146/1688)、2.84%(48/1688)和1.30%(22/1688),采用参比法检测的阳性率分别为8.47%(143/1688)、8.53%(144/1688)、2.78%(47/1688)和1.24%(21/1688),两种方法的一致性均大于99.53%。综上所述,建立了一种灵敏度、特异性和重复性高的四重RT-qPCR方法,可快速、准确地检测CCoV、CRCoV、CAV-2和CNV。
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Establishment of a Quadruplex RT-qPCR for the Detection of Canine Coronavirus, Canine Respiratory Coronavirus, Canine Adenovirus Type 2, and Canine Norovirus.

Canine coronavirus (CCoV), canine respiratory coronavirus (CRCoV), canine adenovirus type 2 (CAV-2), and canine norovirus (CNV) are important pathogens for canine viral gastrointestinal and respiratory diseases. Especially, co-infections with these viruses exacerbate the damages of diseases. In this study, four pairs of primers and probes were designed to specifically amplify the conserved regions of the CCoV M gene, CRCoV N gene, CAV-2 hexon gene, and CNV RdRp gene. After optimizing different reaction conditions, a quadruplex RT-qPCR was established for the detection of CCoV, CRCoV, CAV-2, and CNV. The specificity, sensitivity, and repeatability of the established assay were evaluated. Then, the assay was used to test 1688 clinical samples from pet hospitals in Guangxi province of China during 2022-2024 to validate its clinical applicability. In addition, these samples were also assessed using the reported reference RT-qPCR assays, and the agreements between the developed and reference assays were determined. The results indicated that the quadruplex RT-qPCR could specifically test only CCoV, CRCoV, CAV-2, and CNV, without cross-reaction with other canine viruses. The assay had high sensitivity with limits of detection (LODs) of 1.0 × 102 copies/reaction for CCoV, CRCoV, CAV-2, and CNV. The repeatability was excellent, with intra-assay variability of 0.19-1.31% and inter-assay variability of 0.10-0.88%. The positivity rates of CCoV, CRCoV, CAV-2, and CNV using the developed assay were 8.59% (145/1688), 8.65% (146/1688), 2.84% (48/1688), and 1.30% (22/1688), respectively, while the positivity rates using the reference assays were 8.47% (143/1688), 8.53% (144/1688), 2.78% (47/1688), and 1.24% (21/1688), respectively, with agreements of more than 99.53% between two methods. In conclusion, a quadruplex RT-qPCR with high sensitivity, specificity, and repeatability was developed for rapid, and accurate detection of CCoV, CRCoV, CAV-2, and CNV.

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来源期刊
Pathogens
Pathogens Medicine-Immunology and Allergy
CiteScore
6.40
自引率
8.10%
发文量
1285
审稿时长
17.75 days
期刊介绍: Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
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