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Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assays Targeting SARS-CoV-2

Identifieur interne : 000736 ( 2020/Analysis ); précédent : 000735; suivant : 000737

Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assays Targeting SARS-CoV-2

Auteurs : Gun-Soo Park [Corée du Sud] ; Keunbon Ku [Corée du Sud] ; Seung-Hwa Baek [Corée du Sud] ; Seong-Jun Kim [Corée du Sud] ; Seung Il Kim [Corée du Sud] ; Bum-Tae Kim [Corée du Sud] ; Jin-Soo Maeng [Corée du Sud]

Source :

RBID : PMC:7144851

Abstract

Epidemics of coronavirus disease 2019 (COVID-19) now have >100,000 confirmed cases worldwide. Diagnosis of COVID-19 is currently performed by quantitative RT-PCR methods, but the capacity of quantitative RT-PCR methods is limited by their requirement of high-level facilities and instruments. Herein, reverse transcription loop-mediated isothermal amplification (RT-LAMP) assays to detect genomic RNA of SARS-CoV-2, the causative virus of COVID-19, were developed and evaluated. RT-LAMP assays 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 so that the tests potentially performed in higher throughput.


Url:
DOI: 10.1016/j.jmoldx.2020.03.006
PubMed: 32276051
PubMed Central: 7144851


Affiliations:


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PMC:7144851

Le document en format XML

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<p>Epidemics of coronavirus disease 2019 (COVID-19) now have >100,000 confirmed cases worldwide. Diagnosis of COVID-19 is currently performed by quantitative RT-PCR methods, but the capacity of quantitative RT-PCR methods is limited by their requirement of high-level facilities and instruments. Herein, reverse transcription loop-mediated isothermal amplification (RT-LAMP) assays to detect genomic RNA of SARS-CoV-2, the causative virus of COVID-19, were developed and evaluated. RT-LAMP assays 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 so that the tests potentially performed in higher throughput.</p>
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<name sortKey="Ku, Keunbon" sort="Ku, Keunbon" uniqKey="Ku K" first="Keunbon" last="Ku">Keunbon Ku</name>
<name sortKey="Maeng, Jin Soo" sort="Maeng, Jin Soo" uniqKey="Maeng J" first="Jin-Soo" last="Maeng">Jin-Soo Maeng</name>
<name sortKey="Maeng, Jin Soo" sort="Maeng, Jin Soo" uniqKey="Maeng J" first="Jin-Soo" last="Maeng">Jin-Soo Maeng</name>
<name sortKey="Park, Gun Soo" sort="Park, Gun Soo" uniqKey="Park G" first="Gun-Soo" last="Park">Gun-Soo Park</name>
</country>
</tree>
</affiliations>
</record>

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