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Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assays Targeting Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)

  • Gun Soo Park
  • , Keunbon Ku
  • , Seung Hwa Baek
  • , Seong Jun Kim
  • , Seung Il Kim
  • , Bum Tae Kim
  • , Jin Soo Maeng
  • Korea Research Institute of Chemical Technology
  • Korea Food Research Institute
  • Korea Institute of Toxicology
  • Korea Basic Science Institute

Research output: Contribution to journalArticlepeer-review

339 Scopus citations

Abstract

The coronavirus disease 2019 (COVID-19) pandemic now has >2,000,000 confirmed cases worldwide. COVID-19 is currently diagnosed using quantitative RT-PCR methods, but the capacity of quantitative RT-PCR methods is limited by their requirement of high-level facilities and instruments. We developed and evaluated reverse transcription loop-mediated isothermal amplification (RT-LAMP) assays to detect genomic RNA of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus of COVID-19. RT-LAMP assays reported in this study can detect as low as 100 copies of SARS-CoV-2 RNA. Cross-reactivity of RT-LAMP assays to other human coronaviruses was not observed. A colorimetric detection method was adapted for this RT-LAMP assay to enable higher throughput.

Original languageEnglish
Pages (from-to)729-735
Number of pages7
JournalJournal of Molecular Diagnostics
Volume22
Issue number6
DOIs
StatePublished - Jun 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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