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Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA

INTRODUCTION: The SARS-CoV-2 pandemic of 2020 has resulted in unparalleled requirements for RNA extraction kits and enzymes required for virus detection, leading to global shortages. This has necessitated the exploration of alternative diagnostic options to alleviate supply chain issues. AIM: To est...

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Autores principales: Lee, Jean Y. H., Best, Nickala, McAuley, Julie, Porter, Jessica L., Seemann, Torsten, Schultz, Mark B., Sait, Michelle, Orlando, Nicole, Mercoulia, Karolina, Ballard, Susan A., Druce, Julian, Tran, Thomas, Catton, Mike G., Pryor, Melinda J., Cui, Huanhuan L., Luttick, Angela, McDonald, Sean, Greenhalgh, Arran, Kwong, Jason C., Sherry, Norelle L., Graham, Maryza, Hoang, Tuyet, Herisse, Marion, Pidot, Sacha J., Williamson, Deborah A., Howden, Benjamin P., Monk, Ian R., Stinear, Timothy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7656183/
https://www.ncbi.nlm.nih.gov/pubmed/32755529
http://dx.doi.org/10.1099/jmm.0.001238
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author Lee, Jean Y. H.
Best, Nickala
McAuley, Julie
Porter, Jessica L.
Seemann, Torsten
Schultz, Mark B.
Sait, Michelle
Orlando, Nicole
Mercoulia, Karolina
Ballard, Susan A.
Druce, Julian
Tran, Thomas
Catton, Mike G.
Pryor, Melinda J.
Cui, Huanhuan L.
Luttick, Angela
McDonald, Sean
Greenhalgh, Arran
Kwong, Jason C.
Sherry, Norelle L.
Graham, Maryza
Hoang, Tuyet
Herisse, Marion
Pidot, Sacha J.
Williamson, Deborah A.
Howden, Benjamin P.
Monk, Ian R.
Stinear, Timothy P.
author_facet Lee, Jean Y. H.
Best, Nickala
McAuley, Julie
Porter, Jessica L.
Seemann, Torsten
Schultz, Mark B.
Sait, Michelle
Orlando, Nicole
Mercoulia, Karolina
Ballard, Susan A.
Druce, Julian
Tran, Thomas
Catton, Mike G.
Pryor, Melinda J.
Cui, Huanhuan L.
Luttick, Angela
McDonald, Sean
Greenhalgh, Arran
Kwong, Jason C.
Sherry, Norelle L.
Graham, Maryza
Hoang, Tuyet
Herisse, Marion
Pidot, Sacha J.
Williamson, Deborah A.
Howden, Benjamin P.
Monk, Ian R.
Stinear, Timothy P.
author_sort Lee, Jean Y. H.
collection PubMed
description INTRODUCTION: The SARS-CoV-2 pandemic of 2020 has resulted in unparalleled requirements for RNA extraction kits and enzymes required for virus detection, leading to global shortages. This has necessitated the exploration of alternative diagnostic options to alleviate supply chain issues. AIM: To establish and validate a reverse transcription loop-mediated isothermal amplification (RT- LAMP) assay for the detection of SARS-CoV-2 from nasopharyngeal swabs. METHODOLOGY: We used a commercial RT-LAMP mastermix from OptiGene in combination with a primer set designed to detect the CDC N1 region of the SARS-CoV-2 nucleocapsid (N) gene. A single-tube, single-step fluorescence assay was implemented whereby 1 µl of universal transport medium (UTM) directly from a nasopharyngeal swab could be used as template, bypassing the requirement for RNA purification. Amplification and detection could be conducted in any thermocycler capable of holding 65 °C for 30 min and measure fluorescence in the FAM channel at 1 min intervals. RESULTS: Assay evaluation by assessment of 157 clinical specimens previously screened by E-gene RT-qPCR revealed assay sensitivity and specificity of 87 and 100%, respectively. Results were fast, with an average time-to-positive (Tp) for 93 clinical samples of 14 min (sd±7 min). Using dilutions of SARS-CoV-2 virus spiked into UTM, we also evaluated assay performance against FDA guidelines for implementation of emergency-use diagnostics and established a limit-of-detection of 54 Tissue Culture Infectious Dose 50 per ml (TCID(50) ml(−1)), with satisfactory assay sensitivity and specificity. A comparison of 20 clinical specimens between four laboratories showed excellent interlaboratory concordance; performing equally well on three different, commonly used thermocyclers, pointing to the robustness of the assay. CONCLUSION: With a simplified workflow, The N1 gene Single Tube Optigene LAMP assay (N1-STOP-LAMP) is a powerful, scalable option for specific and rapid detection of SARS-CoV-2 and an additional resource in the diagnostic armamentarium against COVID-19.
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spelling pubmed-76561832020-11-12 Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA Lee, Jean Y. H. Best, Nickala McAuley, Julie Porter, Jessica L. Seemann, Torsten Schultz, Mark B. Sait, Michelle Orlando, Nicole Mercoulia, Karolina Ballard, Susan A. Druce, Julian Tran, Thomas Catton, Mike G. Pryor, Melinda J. Cui, Huanhuan L. Luttick, Angela McDonald, Sean Greenhalgh, Arran Kwong, Jason C. Sherry, Norelle L. Graham, Maryza Hoang, Tuyet Herisse, Marion Pidot, Sacha J. Williamson, Deborah A. Howden, Benjamin P. Monk, Ian R. Stinear, Timothy P. J Med Microbiol Research Article INTRODUCTION: The SARS-CoV-2 pandemic of 2020 has resulted in unparalleled requirements for RNA extraction kits and enzymes required for virus detection, leading to global shortages. This has necessitated the exploration of alternative diagnostic options to alleviate supply chain issues. AIM: To establish and validate a reverse transcription loop-mediated isothermal amplification (RT- LAMP) assay for the detection of SARS-CoV-2 from nasopharyngeal swabs. METHODOLOGY: We used a commercial RT-LAMP mastermix from OptiGene in combination with a primer set designed to detect the CDC N1 region of the SARS-CoV-2 nucleocapsid (N) gene. A single-tube, single-step fluorescence assay was implemented whereby 1 µl of universal transport medium (UTM) directly from a nasopharyngeal swab could be used as template, bypassing the requirement for RNA purification. Amplification and detection could be conducted in any thermocycler capable of holding 65 °C for 30 min and measure fluorescence in the FAM channel at 1 min intervals. RESULTS: Assay evaluation by assessment of 157 clinical specimens previously screened by E-gene RT-qPCR revealed assay sensitivity and specificity of 87 and 100%, respectively. Results were fast, with an average time-to-positive (Tp) for 93 clinical samples of 14 min (sd±7 min). Using dilutions of SARS-CoV-2 virus spiked into UTM, we also evaluated assay performance against FDA guidelines for implementation of emergency-use diagnostics and established a limit-of-detection of 54 Tissue Culture Infectious Dose 50 per ml (TCID(50) ml(−1)), with satisfactory assay sensitivity and specificity. A comparison of 20 clinical specimens between four laboratories showed excellent interlaboratory concordance; performing equally well on three different, commonly used thermocyclers, pointing to the robustness of the assay. CONCLUSION: With a simplified workflow, The N1 gene Single Tube Optigene LAMP assay (N1-STOP-LAMP) is a powerful, scalable option for specific and rapid detection of SARS-CoV-2 and an additional resource in the diagnostic armamentarium against COVID-19. Microbiology Society 2020-09 2020-08-05 /pmc/articles/PMC7656183/ /pubmed/32755529 http://dx.doi.org/10.1099/jmm.0.001238 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Research Article
Lee, Jean Y. H.
Best, Nickala
McAuley, Julie
Porter, Jessica L.
Seemann, Torsten
Schultz, Mark B.
Sait, Michelle
Orlando, Nicole
Mercoulia, Karolina
Ballard, Susan A.
Druce, Julian
Tran, Thomas
Catton, Mike G.
Pryor, Melinda J.
Cui, Huanhuan L.
Luttick, Angela
McDonald, Sean
Greenhalgh, Arran
Kwong, Jason C.
Sherry, Norelle L.
Graham, Maryza
Hoang, Tuyet
Herisse, Marion
Pidot, Sacha J.
Williamson, Deborah A.
Howden, Benjamin P.
Monk, Ian R.
Stinear, Timothy P.
Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title_full Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title_fullStr Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title_full_unstemmed Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title_short Validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of SARS-CoV-2 RNA
title_sort validation of a single-step, single-tube reverse transcription loop-mediated isothermal amplification assay for rapid detection of sars-cov-2 rna
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7656183/
https://www.ncbi.nlm.nih.gov/pubmed/32755529
http://dx.doi.org/10.1099/jmm.0.001238
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