Alvarez Mario Moisés, Bravo-González Sergio, González-González Everardo, Trujillo-de Santiago Grissel
Centro de Biotecnología-FEMSA, Tecnologico de Monterrey, Monterrey 64849, Mexico.
Departamento de Bioingeniería, Tecnologico de Monterrey, Monterrey 64849, Mexico.
Biosensors (Basel). 2021 Oct 13;11(10):386. doi: 10.3390/bios11100386.
Loop-mediated isothermal amplification (LAMP) has been recently studied as an alternative method for cost-effective diagnostics in the context of the current COVID-19 pandemic. Recent reports document that LAMP-based diagnostic methods have a comparable sensitivity and specificity to that of RT-qPCR. We report the use of a portable Arduino-based LAMP-based amplification system assisted by pH microelectrodes for the accurate and reliable diagnosis of SARS-CoV-2 during the first 3 min of the amplification reaction. We show that this simple system enables a straightforward discrimination between samples containing or not containing artificial SARS-CoV-2 genetic material in the range of 10 to 10,000 copies per 50 µL of reaction mix. We also spiked saliva samples with SARS-CoV-2 synthetic material and corroborated that the LAMP reaction can be successfully monitored in real time using microelectrodes in saliva samples as well. These results may have profound implications for the design of real-time and portable quantitative systems for the reliable detection of viral pathogens including SARS-CoV-2.
环介导等温扩增技术(LAMP)最近被作为一种在当前新冠疫情背景下实现经济高效诊断的替代方法进行研究。近期报告表明,基于LAMP的诊断方法与逆转录定量聚合酶链反应(RT-qPCR)具有相当的灵敏度和特异性。我们报告了一种基于便携式Arduino的、由pH微电极辅助的LAMP扩增系统,该系统能够在扩增反应的前3分钟内对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)进行准确可靠的诊断。我们表明,这个简单的系统能够直接区分每50微升反应混合物中含有或不含有10至10000拷贝人工合成SARS-CoV-2遗传物质的样本。我们还向唾液样本中加入了SARS-CoV-2合成材料,并证实也可以使用唾液样本中的微电极实时成功监测LAMP反应。这些结果可能对设计用于可靠检测包括SARS-CoV-2在内的病毒病原体的实时便携式定量系统具有深远意义。