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用于 COVID-19 的便携且准确的诊断:微型 PCR 热循环仪和微孔板读数仪联合用于 SARS-CoV-2 病毒检测。

Portable and accurate diagnostics for COVID-19: Combined use of the miniPCR thermocycler and a well-plate reader for SARS-CoV-2 virus detection.

机构信息

Centro de Biotecnología-FEMSA, Escuela de Ingeniería y Ciencias, Tecnologico de Monterrey, Monterrey, Nuevo León, México.

Departamento de Bioingeniería, Escuela de Ingeniería y Ciencias, Tecnologico de Monterrey, Monterrey, Nuevo León, México.

出版信息

PLoS One. 2020 Aug 13;15(8):e0237418. doi: 10.1371/journal.pone.0237418. eCollection 2020.

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has crudely demonstrated the need for massive and rapid diagnostics. By the first week of July, more than 10,000,000 positive cases of COVID-19 have been reported worldwide, although this number could be greatly underestimated. In the case of an epidemic emergency, the first line of response should be based on commercially available and validated resources. Here, we demonstrate the use of the miniPCR, a commercial compact and portable PCR device recently available on the market, in combination with a commercial well-plate reader as a diagnostic system for detecting genetic material of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causal agent of COVID-19. We used the miniPCR to detect and amplify SARS-CoV-2 DNA sequences using the sets of initiators recommended by the World Health Organization (WHO) for targeting three different regions that encode for the N protein. Prior to amplification, samples were combined with a DNA intercalating reagent (i.e., EvaGreen Dye). Sample fluorescence after amplification was then read using a commercial 96-well plate reader. This straightforward method allows the detection and amplification of SARS-CoV-2 nucleic acids in the range of ~625 to 2×105 DNA copies. The accuracy and simplicity of this diagnostics strategy may provide a cost-efficient and reliable alternative for COVID-19 pandemic testing, particularly in underdeveloped regions where RT-QPCR instrument availability may be limited. The portability, ease of use, and reproducibility of the miniPCR makes it a reliable alternative for deployment in point-of-care SARS-CoV-2 detection efforts during pandemics.

摘要

2019 年冠状病毒病(COVID-19)大流行粗陋地展示了对大量和快速诊断的需求。截至 7 月第一周,全世界已报告超过 1000 万例 COVID-19 阳性病例,尽管这一数字可能被大大低估。在发生疫情紧急情况时,应首先利用商业上可获得和经过验证的资源做出反应。在这里,我们展示了商业紧凑型和便携式 PCR 设备 miniPCR 的使用方法,该设备最近在市场上推出,并结合商业微孔板读数器作为检测严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的遗传物质的诊断系统,SARS-CoV-2 是 COVID-19 的致病因子。我们使用 miniPCR 检测和扩增 SARS-CoV-2 DNA 序列,使用世界卫生组织(WHO)推荐的针对编码 N 蛋白的三个不同区域的起始子集。在扩增之前,将样品与 DNA 嵌入试剂(即 EvaGreen 染料)混合。然后使用商业 96 孔板读数器读取扩增后的样品荧光。这种简单直接的方法允许在 625 到 2×105 DNA 拷贝的范围内检测和扩增 SARS-CoV-2 核酸。该诊断策略的准确性和简单性可能为 COVID-19 大流行测试提供一种具有成本效益且可靠的替代方法,特别是在 RT-QPCR 仪器可用性可能有限的欠发达地区。miniPCR 的便携性、易用性和可重复性使其成为大流行期间在护理点 SARS-CoV-2 检测工作中的可靠替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b319/7425953/9a48f39249e5/pone.0237418.g001.jpg

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