开发新的现场可部署的COVID-19检测RT-qPCR工作流程

Raphael Nyaruaba, Bo Zhang, Caroline Muema, E. Muturi, Greater K., Jin Xiong, Bei Li, Z. Shí, Caroline Mwaliko, Junping Yu, Xiaohong Li, Yanan Zhang, H. Wei
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引用次数: 1

摘要

背景:2019冠状病毒病(COVID-19)在全球不同国家爆发。该病毒具有高度传染性,因此早期发现、隔离和检疫受感染患者将在遏制病毒传播方面发挥重要作用。移动实验室的诊断有助于及时发现受感染的患者。方法:在这里,我们开发了一个可现场部署的诊断工作流程,可以可靠地检测COVID-19。在这个工作流程中使用的仪器可以很容易地安装在移动小屋医院中,也可以安装在社区中。优化从样品失活到检测的不同步骤,寻找检测COVID-19的最快步骤和便携式仪器。每个步骤都与正常的实验室诊断设置进行比较。结果:从结果来看,我们提出的工作流程(80分钟)比正常实验室工作流程(183分钟)快两倍,每次运行最多可检测32个样品。此外,我们发现使用1% Rewocid WK-30可以直接灭活新型冠状病毒,而不会影响整体检测结果。将我们的工作流程与商业获得的分析方法进行比较,产生了高度可靠的结果。在250份医院样本中,两种分析结果的一致性很高(247/250,98.8%)。与商业检测相比,内部检测的敏感性和特异性分别为116/116(100%)和131/134(97.8%)。结论:基于这些结果,我们相信我们的工作流程快速、可靠、适应性强,最重要的是,可在现场部署。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a new field-deployable RT-qPCR workflow for COVID-19 detection
Background: Outbreaks of coronavirus disease 2019 (COVID-19) have been recorded in different countries across the globe. The virus is highly contagious, hence early detection, isolation, and quarantine of infected patients will play an important role in containing the viral spread. Diagnosis in a mobile lab can aid to find infected patients in time. Methods: Here, we develop a field-deployable diagnostic workflow that can reliably detect COVID-19. Instruments used in this workflow can easily fit in a mobile cabin hospital and also be installed in the community. Different steps from sample inactivation to detection were optimized to find the fastest steps and portable instruments in the detection of COVID-19. Each step was compared to that of the normal laboratory diagnosis setup. Results: From the results, our proposed workflow (80 min) was two times faster compared to that of the normal laboratory workflow (183 min) and a maximum of 32 samples could be detected at each run. Additionally, we showed that using 1% Rewocid WK-30 could inactivate the novel coronavirus directly without affecting the overall detection results. Comparison of our workflow using an in-house assay to that of a commercially acquired assay produced highly reliable results. From the 250 hospital samples tested, there was a high concordance 247/250 (98.8%) between the two assays. The in-house assay sensitivity and specificity were 116/116 (100%) and 131/134 (97.8%) compared to that of the commercial assay. Conclusion: Based on these results, we believe that our workflow is fast, reliable, adaptable and most importantly, field-deployable.
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