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An enhanced isothermal amplification assay for viral detection

Rapid, inexpensive, robust diagnostics are essential to control the spread of infectious diseases. Current state of the art diagnostics are highly sensitive and specific, but slow, and require expensive equipment. Here we report the development of a molecular diagnostic test for SARS-CoV-2 based on...

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Autores principales: Qian, Jason, Boswell, Sarah A., Chidley, Christopher, Lu, Zhi-xiang, Pettit, Mary E., Gaudio, Benjamin L., Fajnzylber, Jesse M., Ingram, Ryan T., Ward, Rebecca H., Li, Jonathan Z., Springer, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7679446/
https://www.ncbi.nlm.nih.gov/pubmed/33219228
http://dx.doi.org/10.1038/s41467-020-19258-y
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author Qian, Jason
Boswell, Sarah A.
Chidley, Christopher
Lu, Zhi-xiang
Pettit, Mary E.
Gaudio, Benjamin L.
Fajnzylber, Jesse M.
Ingram, Ryan T.
Ward, Rebecca H.
Li, Jonathan Z.
Springer, Michael
author_facet Qian, Jason
Boswell, Sarah A.
Chidley, Christopher
Lu, Zhi-xiang
Pettit, Mary E.
Gaudio, Benjamin L.
Fajnzylber, Jesse M.
Ingram, Ryan T.
Ward, Rebecca H.
Li, Jonathan Z.
Springer, Michael
author_sort Qian, Jason
collection PubMed
description Rapid, inexpensive, robust diagnostics are essential to control the spread of infectious diseases. Current state of the art diagnostics are highly sensitive and specific, but slow, and require expensive equipment. Here we report the development of a molecular diagnostic test for SARS-CoV-2 based on an enhanced recombinase polymerase amplification (eRPA) reaction. eRPA has a detection limit on patient samples down to 5 viral copies, requires minimal instrumentation, and is highly scalable and inexpensive. eRPA does not cross-react with other common coronaviruses, does not require RNA purification, and takes ~45 min from sample collection to results. eRPA represents a first step toward at-home SARS-CoV-2 detection and can be adapted to future viruses within days of genomic sequence availability.
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spelling pubmed-76794462020-11-24 An enhanced isothermal amplification assay for viral detection Qian, Jason Boswell, Sarah A. Chidley, Christopher Lu, Zhi-xiang Pettit, Mary E. Gaudio, Benjamin L. Fajnzylber, Jesse M. Ingram, Ryan T. Ward, Rebecca H. Li, Jonathan Z. Springer, Michael Nat Commun Article Rapid, inexpensive, robust diagnostics are essential to control the spread of infectious diseases. Current state of the art diagnostics are highly sensitive and specific, but slow, and require expensive equipment. Here we report the development of a molecular diagnostic test for SARS-CoV-2 based on an enhanced recombinase polymerase amplification (eRPA) reaction. eRPA has a detection limit on patient samples down to 5 viral copies, requires minimal instrumentation, and is highly scalable and inexpensive. eRPA does not cross-react with other common coronaviruses, does not require RNA purification, and takes ~45 min from sample collection to results. eRPA represents a first step toward at-home SARS-CoV-2 detection and can be adapted to future viruses within days of genomic sequence availability. Nature Publishing Group UK 2020-11-20 /pmc/articles/PMC7679446/ /pubmed/33219228 http://dx.doi.org/10.1038/s41467-020-19258-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Qian, Jason
Boswell, Sarah A.
Chidley, Christopher
Lu, Zhi-xiang
Pettit, Mary E.
Gaudio, Benjamin L.
Fajnzylber, Jesse M.
Ingram, Ryan T.
Ward, Rebecca H.
Li, Jonathan Z.
Springer, Michael
An enhanced isothermal amplification assay for viral detection
title An enhanced isothermal amplification assay for viral detection
title_full An enhanced isothermal amplification assay for viral detection
title_fullStr An enhanced isothermal amplification assay for viral detection
title_full_unstemmed An enhanced isothermal amplification assay for viral detection
title_short An enhanced isothermal amplification assay for viral detection
title_sort enhanced isothermal amplification assay for viral detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7679446/
https://www.ncbi.nlm.nih.gov/pubmed/33219228
http://dx.doi.org/10.1038/s41467-020-19258-y
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