4.7 Article

Rapid and Visual Detection of SARS-CoV-2 Using Multiplex Reverse Transcription Loop-Mediated Isothermal Amplification Linked With Gold Nanoparticle-Based Lateral Flow Biosensor

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.581239

关键词

lateral flow biosensor; reverse transcription-loop-mediated isothermal amplification; limit of detection; COVID-19; SARS-CoV-2

资金

  1. Program of Scientific and Technological Project in Guizhou Province [[2020] 4Y184, [2019] 1186, [2020]4Y197]
  2. Scientific and Technological in Guiyang City [[2020]-10-5, [2020]-16-5]
  3. Program of Scientific and Technological Innovation Team of Guizhou Province [[2018]5606]
  4. Public Welfare Technology Application Research Program of Zhejiang Province [LGF21H190001]
  5. National Natural Science Foundation of China [81801978]

向作者/读者索取更多资源

The novel molecular diagnosis technique, multiplex reverse transcription loop-mediated isothermal amplification (mRT-LAMP) combined with a nanoparticle-based lateral flow biosensor, demonstrated high sensitivity and specificity in detecting the SARS-CoV-2 virus. The mRT-LAMP-LFB method is a simple, rapid, and reliable assay for identifying SARS-CoV-2, especially in resource-constrained regions for prevention and control of COVID-19.
Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel coronavirus that has caused the outbreak of coronavirus disease 2019 (COVID-19) all over the world. In the absence of appropriate antiviral drugs or vaccines, developing a simple, rapid, and reliable assay for SARS-CoV-2 is necessary for the prevention and control of the COVID-19 transmission. Methods A novel molecular diagnosis technique, named multiplex reverse transcription loop-mediated isothermal amplification, that has been linked to a nanoparticle-based lateral flow biosensor (mRT-LAMP-LFB) was applied to detect SARS-CoV-2 based on the SARS-CoV-2 RdRp and N genes, and the mRT-LAMP products were analyzed using nanoparticle-based lateral flow biosensor. The mRT-LAMP-LFB amplification conditions, including the target RNA concentration, amplification temperature, and time were optimized. The sensitivity and specificity of the mRT-LAMP-LFB method were tested in the current study, and the mRT-LAMP-LFB assay was applied to detect the SARS-CoV-2 virus from clinical samples and artificial sputum samples. Results The SARS-CoV-2 specific primers based on the RdRp and N genes were valid for the establishment of mRT-LAMP-LFB assay to detect the SARS-CoV-2 virus. The multiple-RT-LAMP amplification condition was optimized at 63 degrees C for 30 min. The full process, including reaction preparation, viral RNA extraction, RT-LAMP, and product identification, could be achieved in 80 min. The limit of detection (LoD) of the mRT-LAMP-LFB technology was 20 copies per reaction. The specificity of mRT-LAMP-LFB detection was 100%, and no cross-reactions to other respiratory pathogens were observed. Conclusion The mRT-LAMP-LFB technique developed in the current study is a simple, rapid, and reliable method with great specificity and sensitivity when it comes to identifying SARS-CoV-2 virus for prevention and control of the COVID-19 disease, especially in resource-constrained regions of the world.

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