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Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification

Fast, inexpensive, and multiplexed detection of multiple nucleic acids is of great importance to human health, yet it still represents a significant challenge. Herein, we propose a nucleic acid testing platform, named MiCaR, which couples a microfluidic device with CRISPR-Cas12a and multiplex recomb...

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Autores principales: Xu, Zhichen, Chen, Dongjuan, Li, Tao, Yan, Jiayu, Zhu, Jiang, He, Ting, Hu, Rui, Li, Ying, Yang, Yunhuang, Liu, Maili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617605/
https://www.ncbi.nlm.nih.gov/pubmed/36309521
http://dx.doi.org/10.1038/s41467-022-34086-y
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author Xu, Zhichen
Chen, Dongjuan
Li, Tao
Yan, Jiayu
Zhu, Jiang
He, Ting
Hu, Rui
Li, Ying
Yang, Yunhuang
Liu, Maili
author_facet Xu, Zhichen
Chen, Dongjuan
Li, Tao
Yan, Jiayu
Zhu, Jiang
He, Ting
Hu, Rui
Li, Ying
Yang, Yunhuang
Liu, Maili
author_sort Xu, Zhichen
collection PubMed
description Fast, inexpensive, and multiplexed detection of multiple nucleic acids is of great importance to human health, yet it still represents a significant challenge. Herein, we propose a nucleic acid testing platform, named MiCaR, which couples a microfluidic device with CRISPR-Cas12a and multiplex recombinase polymerase amplification. With only one fluorescence probe, MiCaR can simultaneously test up to 30 nucleic acid targets through microfluidic space coding. The detection limit achieves 0.26 attomole, and the multiplexed assay takes only 40 min. We demonstrate the utility of MiCaR by efficiently detecting the nine HPV subtypes targeted by the 9-valent HPV vaccine, showing a sensitivity of 97.8% and specificity of 98.1% in the testing of 100 patient samples at risk for HPV infection. Additionally, we also show the generalizability of our approach by successfully testing eight of the most clinically relevant respiratory viruses. We anticipate this effective, undecorated and versatile platform to be widely used in multiplexed nucleic acid detection.
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spelling pubmed-96176052022-10-31 Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification Xu, Zhichen Chen, Dongjuan Li, Tao Yan, Jiayu Zhu, Jiang He, Ting Hu, Rui Li, Ying Yang, Yunhuang Liu, Maili Nat Commun Article Fast, inexpensive, and multiplexed detection of multiple nucleic acids is of great importance to human health, yet it still represents a significant challenge. Herein, we propose a nucleic acid testing platform, named MiCaR, which couples a microfluidic device with CRISPR-Cas12a and multiplex recombinase polymerase amplification. With only one fluorescence probe, MiCaR can simultaneously test up to 30 nucleic acid targets through microfluidic space coding. The detection limit achieves 0.26 attomole, and the multiplexed assay takes only 40 min. We demonstrate the utility of MiCaR by efficiently detecting the nine HPV subtypes targeted by the 9-valent HPV vaccine, showing a sensitivity of 97.8% and specificity of 98.1% in the testing of 100 patient samples at risk for HPV infection. Additionally, we also show the generalizability of our approach by successfully testing eight of the most clinically relevant respiratory viruses. We anticipate this effective, undecorated and versatile platform to be widely used in multiplexed nucleic acid detection. Nature Publishing Group UK 2022-10-29 /pmc/articles/PMC9617605/ /pubmed/36309521 http://dx.doi.org/10.1038/s41467-022-34086-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xu, Zhichen
Chen, Dongjuan
Li, Tao
Yan, Jiayu
Zhu, Jiang
He, Ting
Hu, Rui
Li, Ying
Yang, Yunhuang
Liu, Maili
Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title_full Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title_fullStr Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title_full_unstemmed Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title_short Microfluidic space coding for multiplexed nucleic acid detection via CRISPR-Cas12a and recombinase polymerase amplification
title_sort microfluidic space coding for multiplexed nucleic acid detection via crispr-cas12a and recombinase polymerase amplification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617605/
https://www.ncbi.nlm.nih.gov/pubmed/36309521
http://dx.doi.org/10.1038/s41467-022-34086-y
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