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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7679446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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