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A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the unprecedented global pandemic of coronavirus disease-2019 (COVID-19). Efforts are needed to develop rapid and accurate diagnostic tools for extensive testing, allowing for effective containment of the infection via timely id...

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Detalles Bibliográficos
Autores principales: Rodriguez-Mateos, Pablo, Ngamsom, Bongkot, Walter, Cheryl, Dyer, Charlotte E., Gitaka, Jesse, Iles, Alexander, Pamme, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202086/
https://www.ncbi.nlm.nih.gov/pubmed/34482896
http://dx.doi.org/10.1016/j.aca.2021.338758
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author Rodriguez-Mateos, Pablo
Ngamsom, Bongkot
Walter, Cheryl
Dyer, Charlotte E.
Gitaka, Jesse
Iles, Alexander
Pamme, Nicole
author_facet Rodriguez-Mateos, Pablo
Ngamsom, Bongkot
Walter, Cheryl
Dyer, Charlotte E.
Gitaka, Jesse
Iles, Alexander
Pamme, Nicole
author_sort Rodriguez-Mateos, Pablo
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the unprecedented global pandemic of coronavirus disease-2019 (COVID-19). Efforts are needed to develop rapid and accurate diagnostic tools for extensive testing, allowing for effective containment of the infection via timely identification and isolation of SARS-CoV-2 carriers. Current gold standard nucleic acid tests require many separate steps that need trained personnel to operate specialist instrumentation in laboratory environments, hampering turnaround time and test accessibility, especially in low-resource settings. We devised an integrated on-chip platform coupling RNA extraction based on immiscible filtration assisted by surface tension (IFAST), with RNA amplification and detection via colorimetric reverse-transcription loop mediated isothermal amplification (RT-LAMP), using two sets of primers targeting open reading frame 1a (ORF1a) and nucleoprotein (N) genes of SARS-CoV-2. Results were identified visually, with a colour change from pink to yellow indicating positive amplification, and further confirmed by DNA gel electrophoresis. The specificity of the assay was tested against HCoV-OC43 and H1N1 RNAs. The assay based on use of gene N primers was 100% specific to SARS-CoV-2 with no cross-reactivity to HCoV-OC43 nor H1N1. Proof-of-concept studies on water and artificial sputum containing genomic SARS-CoV-2 RNA showed our IFAST RT-LAMP device to be capable of extracting and detecting 470 SARS-CoV-2 copies mL(−1) within 1 h (from sample-in to answer-out). IFAST RT-LAMP is a simple-to-use, integrated, rapid and accurate COVID-19 diagnostic platform, which could provide an attractive means for extensive screening of SARS-CoV-2 infections at point-of-care, especially in resource-constrained settings.
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spelling pubmed-82020862021-06-15 A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings Rodriguez-Mateos, Pablo Ngamsom, Bongkot Walter, Cheryl Dyer, Charlotte E. Gitaka, Jesse Iles, Alexander Pamme, Nicole Anal Chim Acta Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused the unprecedented global pandemic of coronavirus disease-2019 (COVID-19). Efforts are needed to develop rapid and accurate diagnostic tools for extensive testing, allowing for effective containment of the infection via timely identification and isolation of SARS-CoV-2 carriers. Current gold standard nucleic acid tests require many separate steps that need trained personnel to operate specialist instrumentation in laboratory environments, hampering turnaround time and test accessibility, especially in low-resource settings. We devised an integrated on-chip platform coupling RNA extraction based on immiscible filtration assisted by surface tension (IFAST), with RNA amplification and detection via colorimetric reverse-transcription loop mediated isothermal amplification (RT-LAMP), using two sets of primers targeting open reading frame 1a (ORF1a) and nucleoprotein (N) genes of SARS-CoV-2. Results were identified visually, with a colour change from pink to yellow indicating positive amplification, and further confirmed by DNA gel electrophoresis. The specificity of the assay was tested against HCoV-OC43 and H1N1 RNAs. The assay based on use of gene N primers was 100% specific to SARS-CoV-2 with no cross-reactivity to HCoV-OC43 nor H1N1. Proof-of-concept studies on water and artificial sputum containing genomic SARS-CoV-2 RNA showed our IFAST RT-LAMP device to be capable of extracting and detecting 470 SARS-CoV-2 copies mL(−1) within 1 h (from sample-in to answer-out). IFAST RT-LAMP is a simple-to-use, integrated, rapid and accurate COVID-19 diagnostic platform, which could provide an attractive means for extensive screening of SARS-CoV-2 infections at point-of-care, especially in resource-constrained settings. Elsevier B.V. 2021-09-08 2021-06-14 /pmc/articles/PMC8202086/ /pubmed/34482896 http://dx.doi.org/10.1016/j.aca.2021.338758 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rodriguez-Mateos, Pablo
Ngamsom, Bongkot
Walter, Cheryl
Dyer, Charlotte E.
Gitaka, Jesse
Iles, Alexander
Pamme, Nicole
A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title_full A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title_fullStr A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title_full_unstemmed A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title_short A lab-on-a-chip platform for integrated extraction and detection of SARS-CoV-2 RNA in resource-limited settings
title_sort lab-on-a-chip platform for integrated extraction and detection of sars-cov-2 rna in resource-limited settings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8202086/
https://www.ncbi.nlm.nih.gov/pubmed/34482896
http://dx.doi.org/10.1016/j.aca.2021.338758
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