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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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. |
format | Online Article Text |
id | pubmed-10312858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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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