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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...

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Autores principales: Zhou, Lifeng, Chandrasekaran, Arun Richard, Punnoose, Jibin Abraham, Bonenfant, Gaston, Charles, Stephon, Levchenko, Oksana, Badu, Pheonah, Cavaliere, Cassandra, Pager, Cara T., Halvorsen, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
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.
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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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