Development of Rapid Isothermal Detection Methods Real-Time Fluorescence and Lateral Flow Reverse Transcription Recombinase-Aided Amplification Assay for Bovine Coronavirus

Qingqing Li, Yan Pan, Cuilan Wu, Chunxia Ma, Jun Li, Changting Li, Huili Bai, Yu Gong, Jing Liu, Li Tao, Yangyan Yin, Ling Teng, Shuhong Zhong, Meiyi Lan, Shuai Hu, Xiong-biao Xuan, Tianchao Wei, Hao Peng
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Abstract

Bovine coronavirus (BCoV) is a notable pathogen affecting newly born calves and adult cattle, increasing mortality rates among calves and reducing productivity in meat and dairy industries, thereby causing substantial economic losses. Current primary laboratory methods for detecting BCoV include RT-PCR assay, real-time RT-PCR assay, and ELISA. However, these methods are time-consuming, require specialized technicians, and necessitate a laboratory environment. Consequently, there is an urgent need for a rapid, sensitive, and easy to use diagnostic method to detect BCoV. This study introduces two innovative protocols: the real-time fluorescent reverse transcription recombinase-aided amplification (RT-RAA) and the test strip RT-RAA (RT-RAA-LFD). Our results indicate that real-time RT-RAA can complete the reaction in 20 min at 39°C, while RT-RAA-LFD can achieve detection in just 17.5 min at 35°C. These new approaches offer higher specificity, with no cross-reactivity to other viruses, and significantly enhanced sensitivity compared to existing methods (1.46 × 101 and 1.46 × 102 copies/μL, respectively). We evaluated the performance of our methods using 242 clinical samples, and compared with RT-PCR and RT-qPCR. Both real-time RT-RAA and RT-qPCR yielded similar detection rates, the detection rate of RT-RAA-LFD was better than RT-PCR. The RT-RAA methods developed in this study effectively overcome the limitations associated with both RT-PCR and RT-qPCR by offering advantages including a single, low reaction temperature that allows for room temperature operation. Both methods boast shorter reaction times, simpler and more portable instrumentation, as well as reduced technical and environmental demands. Generally, both RT-RAA methods established in this study offer new avenues for the rapid detection of BCoV, contributing significantly to the monitoring, prevention, and control of the disease in global bovine industry.
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开发牛冠状病毒实时荧光和侧流反转录重组酶辅助扩增测定的快速等温检测方法
牛冠状病毒(BCoV)是影响新生犊牛和成年牛的一种显著病原体,会增加犊牛的死亡率,降低肉类和乳制品行业的生产率,从而造成巨大的经济损失。目前实验室检测 BCoV 的主要方法包括 RT-PCR 法、实时 RT-PCR 法和 ELISA 法。然而,这些方法耗时长,需要专业技术人员,而且必须有实验室环境。因此,目前急需一种快速、灵敏、简便的诊断方法来检测 BCoV。本研究引入了两种创新方案:实时荧光反转录重组酶辅助扩增(RT-RAA)和试纸RT-RAA(RT-RAA-LFD)。我们的研究结果表明,实时 RT-RAA 在 39°C 下 20 分钟内即可完成反应,而 RT-RAA-LFD 在 35°C 下仅需 17.5 分钟即可实现检测。与现有方法相比,这些新方法具有更高的特异性,不会与其他病毒产生交叉反应,灵敏度也显著提高(分别为 1.46 × 101 和 1.46 × 102 拷贝/μL)。我们使用 242 份临床样本评估了我们方法的性能,并与 RT-PCR 和 RT-qPCR 进行了比较。实时 RT-RAA 和 RT-qPCR 的检出率相似,RT-RAA-LFD 的检出率优于 RT-PCR。本研究开发的 RT-RAA 方法有效克服了 RT-PCR 和 RT-qPCR 的局限性,其优点包括反应温度低,可在室温下操作。这两种方法都具有反应时间更短、仪器更简单便携、技术和环境要求更低等优点。总体而言,本研究中建立的两种 RT-RAA 方法都为快速检测 BCoV 提供了新的途径,为全球牛业的疾病监测、预防和控制做出了重要贡献。
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