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Programmable low-cost DNA-based platform for viral RNA detection
Detection of viruses is critical for controlling disease spread. Recent emerging viral threats, including Zika virus, Ebola virus, and SARS-CoV-2 responsible for coronavirus disease 2019 (COVID-19) highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a pla...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518872/ https://www.ncbi.nlm.nih.gov/pubmed/32978154 http://dx.doi.org/10.1126/sciadv.abc6246 |
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author | Zhou, Lifeng Chandrasekaran, Arun Richard Punnoose, Jibin Abraham Bonenfant, Gaston Charles, Stephon Levchenko, Oksana Badu, Pheonah Cavaliere, Cassandra Pager, Cara T. Halvorsen, Ken |
author_facet | Zhou, Lifeng Chandrasekaran, Arun Richard Punnoose, Jibin Abraham Bonenfant, Gaston Charles, Stephon Levchenko, Oksana Badu, Pheonah Cavaliere, Cassandra Pager, Cara T. Halvorsen, Ken |
author_sort | Zhou, Lifeng |
collection | PubMed |
description | Detection of viruses is critical for controlling disease spread. Recent emerging viral threats, including Zika virus, Ebola virus, and SARS-CoV-2 responsible for coronavirus disease 2019 (COVID-19) highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show nonenzymatic detection of viral RNA with selective and multiplexed detection between related viruses and viral strains. For clinical-level sensitivity in biological fluids, we paired the assay with sample preparation using either RNA extraction or isothermal preamplification. Our assay requires minimal laboratory infrastructure and is adaptable to other viruses, as demonstrated by quickly developing DNA nanoswitches to detect SARS-CoV-2 RNA in saliva. Further development and field implementation will improve our ability to detect emergent viral threats and ultimately limit their impact. |
format | Online Article Text |
id | pubmed-7518872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75188722020-10-02 Programmable low-cost DNA-based platform for viral RNA detection Zhou, Lifeng Chandrasekaran, Arun Richard Punnoose, Jibin Abraham Bonenfant, Gaston Charles, Stephon Levchenko, Oksana Badu, Pheonah Cavaliere, Cassandra Pager, Cara T. Halvorsen, Ken Sci Adv Research Articles Detection of viruses is critical for controlling disease spread. Recent emerging viral threats, including Zika virus, Ebola virus, and SARS-CoV-2 responsible for coronavirus disease 2019 (COVID-19) highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show nonenzymatic detection of viral RNA with selective and multiplexed detection between related viruses and viral strains. For clinical-level sensitivity in biological fluids, we paired the assay with sample preparation using either RNA extraction or isothermal preamplification. Our assay requires minimal laboratory infrastructure and is adaptable to other viruses, as demonstrated by quickly developing DNA nanoswitches to detect SARS-CoV-2 RNA in saliva. Further development and field implementation will improve our ability to detect emergent viral threats and ultimately limit their impact. American Association for the Advancement of Science 2020-09-25 /pmc/articles/PMC7518872/ /pubmed/32978154 http://dx.doi.org/10.1126/sciadv.abc6246 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zhou, Lifeng Chandrasekaran, Arun Richard Punnoose, Jibin Abraham Bonenfant, Gaston Charles, Stephon Levchenko, Oksana Badu, Pheonah Cavaliere, Cassandra Pager, Cara T. Halvorsen, Ken Programmable low-cost DNA-based platform for viral RNA detection |
title | Programmable low-cost DNA-based platform for viral RNA detection |
title_full | Programmable low-cost DNA-based platform for viral RNA detection |
title_fullStr | Programmable low-cost DNA-based platform for viral RNA detection |
title_full_unstemmed | Programmable low-cost DNA-based platform for viral RNA detection |
title_short | Programmable low-cost DNA-based platform for viral RNA detection |
title_sort | programmable low-cost dna-based platform for viral rna detection |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7518872/ https://www.ncbi.nlm.nih.gov/pubmed/32978154 http://dx.doi.org/10.1126/sciadv.abc6246 |
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