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Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens
Rapid screening and low-cost diagnosis play a crucial role in choosing the correct course of intervention when dealing with highly infectious pathogens. This is especially important if the disease-causing agent has no effective treatment, such as the novel coronavirus SARS-CoV-2, and shows no or sim...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710731/ https://www.ncbi.nlm.nih.gov/pubmed/33268779 http://dx.doi.org/10.1038/s41467-020-19911-6 |
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author | Nunez-Bajo, Estefania Silva Pinto Collins, Alexander Kasimatis, Michael Cotur, Yasin Asfour, Tarek Tanriverdi, Ugur Grell, Max Kaisti, Matti Senesi, Guglielmo Stevenson, Karen Güder, Firat |
author_facet | Nunez-Bajo, Estefania Silva Pinto Collins, Alexander Kasimatis, Michael Cotur, Yasin Asfour, Tarek Tanriverdi, Ugur Grell, Max Kaisti, Matti Senesi, Guglielmo Stevenson, Karen Güder, Firat |
author_sort | Nunez-Bajo, Estefania |
collection | PubMed |
description | Rapid screening and low-cost diagnosis play a crucial role in choosing the correct course of intervention when dealing with highly infectious pathogens. This is especially important if the disease-causing agent has no effective treatment, such as the novel coronavirus SARS-CoV-2, and shows no or similar symptoms to other common infections. Here, we report a disposable silicon-based integrated Point-of-Need transducer (TriSilix) for real-time quantitative detection of pathogen-specific sequences of nucleic acids. TriSilix can be produced at wafer-scale in a standard laboratory (37 chips of 10 × 10 × 0.65 mm in size can be produced in 7 h, costing ~0.35 USD per device). We are able to quantitatively detect a 563 bp fragment of genomic DNA of Mycobacterium avium subspecies paratuberculosis through real-time PCR with a limit-of-detection of 20 fg, equivalent to a single bacterium, at the 35(th) cycle. Using TriSilix, we also detect the cDNA from SARS-CoV-2 (1 pg) with high specificity against SARS-CoV (2003). |
format | Online Article Text |
id | pubmed-7710731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77107312020-12-03 Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens Nunez-Bajo, Estefania Silva Pinto Collins, Alexander Kasimatis, Michael Cotur, Yasin Asfour, Tarek Tanriverdi, Ugur Grell, Max Kaisti, Matti Senesi, Guglielmo Stevenson, Karen Güder, Firat Nat Commun Article Rapid screening and low-cost diagnosis play a crucial role in choosing the correct course of intervention when dealing with highly infectious pathogens. This is especially important if the disease-causing agent has no effective treatment, such as the novel coronavirus SARS-CoV-2, and shows no or similar symptoms to other common infections. Here, we report a disposable silicon-based integrated Point-of-Need transducer (TriSilix) for real-time quantitative detection of pathogen-specific sequences of nucleic acids. TriSilix can be produced at wafer-scale in a standard laboratory (37 chips of 10 × 10 × 0.65 mm in size can be produced in 7 h, costing ~0.35 USD per device). We are able to quantitatively detect a 563 bp fragment of genomic DNA of Mycobacterium avium subspecies paratuberculosis through real-time PCR with a limit-of-detection of 20 fg, equivalent to a single bacterium, at the 35(th) cycle. Using TriSilix, we also detect the cDNA from SARS-CoV-2 (1 pg) with high specificity against SARS-CoV (2003). Nature Publishing Group UK 2020-12-02 /pmc/articles/PMC7710731/ /pubmed/33268779 http://dx.doi.org/10.1038/s41467-020-19911-6 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Nunez-Bajo, Estefania Silva Pinto Collins, Alexander Kasimatis, Michael Cotur, Yasin Asfour, Tarek Tanriverdi, Ugur Grell, Max Kaisti, Matti Senesi, Guglielmo Stevenson, Karen Güder, Firat Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title | Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title_full | Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title_fullStr | Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title_full_unstemmed | Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title_short | Disposable silicon-based all-in-one micro-qPCR for apid on-site detection of pathogens |
title_sort | disposable silicon-based all-in-one micro-qpcr for apid on-site detection of pathogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710731/ https://www.ncbi.nlm.nih.gov/pubmed/33268779 http://dx.doi.org/10.1038/s41467-020-19911-6 |
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