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A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches

The emergence of a highly contagious novel coronavirus in 2019 led to an unprecedented need for large scale diagnostic testing. The associated challenges including reagent shortages, cost, deployment delays, and turnaround time have all highlighted the need for an alternative suite of low-cost tests...

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Autores principales: Vilcapoma, Javier, Aliyeva, Asmer, Hayden, Andrew, Chandrasekaran, Arun Richard, Zhou, Lifeng, Punnoose, Jibin Abraham, Yang, Darren, Hansen, Clinton, Shiu, Simon Chi-Chin, Russell, Alexis, George, Kirsten St., Wong, Wesley P., Halvorsen, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312858/
https://www.ncbi.nlm.nih.gov/pubmed/37398235
http://dx.doi.org/10.1101/2023.05.31.23290613
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author Vilcapoma, Javier
Aliyeva, Asmer
Hayden, Andrew
Chandrasekaran, Arun Richard
Zhou, Lifeng
Punnoose, Jibin Abraham
Yang, Darren
Hansen, Clinton
Shiu, Simon Chi-Chin
Russell, Alexis
George, Kirsten St.
Wong, Wesley P.
Halvorsen, Ken
author_facet Vilcapoma, Javier
Aliyeva, Asmer
Hayden, Andrew
Chandrasekaran, Arun Richard
Zhou, Lifeng
Punnoose, Jibin Abraham
Yang, Darren
Hansen, Clinton
Shiu, Simon Chi-Chin
Russell, Alexis
George, Kirsten St.
Wong, Wesley P.
Halvorsen, Ken
author_sort Vilcapoma, Javier
collection PubMed
description The emergence of a highly contagious novel coronavirus in 2019 led to an unprecedented need for large scale diagnostic testing. The associated challenges including reagent shortages, cost, deployment delays, and turnaround time have all highlighted the need for an alternative suite of low-cost tests. Here, we demonstrate a diagnostic test for SARS-CoV-2 RNA that provides direct detection of viral RNA and eliminates the need for costly enzymes. We employ DNA nanoswitches that respond to segments of the viral RNA by a change in shape that is readable by gel electrophoresis. A new multi-targeting approach samples 120 different viral regions to improve the limit of detection and provide robust detection of viral variants. We apply our approach to a cohort of clinical samples, positively identifying a subset of samples with high viral loads. Since our method directly detects multiple regions of viral RNA without amplification, it eliminates the risk of amplicon contamination and renders the method less susceptible to false positives. This new tool can benefit the COVID-19 pandemic and future emerging outbreaks, providing a third option between amplification-based RNA detection and protein antigen detection. Ultimately, we believe this tool can be adapted both for low-resource onsite testing as well as for monitoring viral loads in recovering patients.
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spelling pubmed-103128582023-07-01 A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches Vilcapoma, Javier Aliyeva, Asmer Hayden, Andrew Chandrasekaran, Arun Richard Zhou, Lifeng Punnoose, Jibin Abraham Yang, Darren Hansen, Clinton Shiu, Simon Chi-Chin Russell, Alexis George, Kirsten St. Wong, Wesley P. Halvorsen, Ken medRxiv Article The emergence of a highly contagious novel coronavirus in 2019 led to an unprecedented need for large scale diagnostic testing. The associated challenges including reagent shortages, cost, deployment delays, and turnaround time have all highlighted the need for an alternative suite of low-cost tests. Here, we demonstrate a diagnostic test for SARS-CoV-2 RNA that provides direct detection of viral RNA and eliminates the need for costly enzymes. We employ DNA nanoswitches that respond to segments of the viral RNA by a change in shape that is readable by gel electrophoresis. A new multi-targeting approach samples 120 different viral regions to improve the limit of detection and provide robust detection of viral variants. We apply our approach to a cohort of clinical samples, positively identifying a subset of samples with high viral loads. Since our method directly detects multiple regions of viral RNA without amplification, it eliminates the risk of amplicon contamination and renders the method less susceptible to false positives. This new tool can benefit the COVID-19 pandemic and future emerging outbreaks, providing a third option between amplification-based RNA detection and protein antigen detection. Ultimately, we believe this tool can be adapted both for low-resource onsite testing as well as for monitoring viral loads in recovering patients. Cold Spring Harbor Laboratory 2023-06-04 /pmc/articles/PMC10312858/ /pubmed/37398235 http://dx.doi.org/10.1101/2023.05.31.23290613 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Vilcapoma, Javier
Aliyeva, Asmer
Hayden, Andrew
Chandrasekaran, Arun Richard
Zhou, Lifeng
Punnoose, Jibin Abraham
Yang, Darren
Hansen, Clinton
Shiu, Simon Chi-Chin
Russell, Alexis
George, Kirsten St.
Wong, Wesley P.
Halvorsen, Ken
A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title_full A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title_fullStr A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title_full_unstemmed A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title_short A non-enzymatic test for SARS-CoV-2 RNA using DNA nanoswitches
title_sort non-enzymatic test for sars-cov-2 rna using dna nanoswitches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312858/
https://www.ncbi.nlm.nih.gov/pubmed/37398235
http://dx.doi.org/10.1101/2023.05.31.23290613
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