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首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
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Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA

机译:用于单步,单管逆转录回路介导的等温扩增测定,用于快速检测SARS-COV-2 RNA

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Introduction The SARS-CoV-2 pandemic of 2020 has resulted in unparalleled requirements for RNA extraction kits and enzymes required for virus detection, leading to global shortages. This has necessitated the exploration of alternative diagnostic options to alleviate supply chain issues. Aim To establish and validate a reverse transcription loop-mediated isothermal amplification (RT- LAMP) assay for the detection of SARS-CoV-2 from nasopharyngeal swabs. Methodology We used a commercial RT-LAMP mastermix from OptiGene in combination with a primer set designed to detect the CDC N1 region of the SARS-CoV-2 nucleocapsid (N) gene. A single-tube, single-step fluorescence assay was implemented whereby 1 μl of universal transport medium (UTM) directly from a nasopharyngeal swab could be used as template, bypassing the requirement for RNA purification. Amplification and detection could be conducted in any thermocycler capable of holding 65 °C for 30 min and measure fluorescence in the FAM channel at 1 min intervals. Results Assay evaluation by assessment of 157 clinical specimens previously screened by E-gene RT-qPCR revealed assay sensitivity and specificity of 87 and 100%, respectively. Results were fast, with an average time-to-positive (Tp) for 93 clinical samples of 14 min ( sd ±7 min). Using dilutions of SARS-CoV-2 virus spiked into UTM, we also evaluated assay performance against FDA guidelines for implementation of emergency-use diagnostics and established a limit-of-detection of 54 Tissue Culture Infectious Dose 50 per ml (TCID _(50) ml ~(?1)), with satisfactory assay sensitivity and specificity. A comparison of 20 clinical specimens between four laboratories showed excellent interlaboratory concordance; performing equally well on three different, commonly used thermocyclers, pointing to the robustness of the assay. Conclusion With a simplified workflow, The N1 gene Single Tube Optigene LAMP assay (N1-STOP-LAMP) is a powerful, scalable option for specific and rapid detection of SARS-CoV-2 and an additional resource in the diagnostic armamentarium against COVID-19.
机译:引言SARS-COV-2 2020的大流行导致了对病毒检测所需的RNA提取套件和酶的无与伦比的要求,导致全球短缺。这需要探索替代诊断选择来缓解供应链问题。旨在建立和验证逆转录回归介导的等温扩增(RT-灯)测定,用于检测来自鼻咽拭子的SARS-COV-2。方法我们使用来自Optigene的商业RT-Lamp Mastermix与设计用于检测SARS-COV-2核衣壳(N)基因的CDC N1区域的引物集合。实施单管,单步荧光测定,从而直接来自鼻咽拭子的1μl通用运输培养基(UTM)作为模板,绕过RNA纯化的要求。扩增和检测可以在任何热循环器中进行,能够保持65℃的30分钟,并以1分钟间隔测量FAM通道中的荧光。结果评估通过E-GeneTRT-QPCR以前筛选的157种临床标本评估分别揭示了87和100%的测定敏感性和特异性。结果快速,平均时间 - 阳性(TP)为93个临床样品14分钟(SD±7分钟)。使用SARS-COV-2病毒的稀释液掺入UTM,我们还评估了针对FDA实施的测定性能,以实施紧急使用诊断,并确定54个组织培养感染剂量50每mL(TCID _(50 )ml〜(α1)),令人满意的测定敏感性和特异性。四个实验室之间的20个临床标本的比较显示出优异的间接性协调;在三种不同,常用的热循环仪上表现得同样良好,指向测定的稳健性。结论具有简化的工作流程,N1基因单管内外灯测定(N1-止挡灯)是一种强大,可伸缩的选择,可用于SARS-COV-2的特定和快速检测,以及对Covid-19的诊断武器中的额外资源。

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