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A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing

The outbreak of virus-induced infectious diseases poses a global public-health challenge. Nucleic acid amplification testing (NAAT) enables early detection of pandemic viruses and plays a vital role in preventing onward transmission. However, the requirement of skilled operators, expensive instrumen...

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Autores principales: Tian, Fei, Liu, Chao, Deng, Jinqi, Han, Ziwei, Zhang, Lu, Chen, Qinghua, Sun, Jiashu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science China Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387882/
https://www.ncbi.nlm.nih.gov/pubmed/32837510
http://dx.doi.org/10.1007/s11426-020-9800-6
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author Tian, Fei
Liu, Chao
Deng, Jinqi
Han, Ziwei
Zhang, Lu
Chen, Qinghua
Sun, Jiashu
author_facet Tian, Fei
Liu, Chao
Deng, Jinqi
Han, Ziwei
Zhang, Lu
Chen, Qinghua
Sun, Jiashu
author_sort Tian, Fei
collection PubMed
description The outbreak of virus-induced infectious diseases poses a global public-health challenge. Nucleic acid amplification testing (NAAT) enables early detection of pandemic viruses and plays a vital role in preventing onward transmission. However, the requirement of skilled operators, expensive instrumentation, and biosafety laboratories has hindered the use of NAAT for screening and diagnosis of suspected patients. Here we report development of a fully automated centrifugal microfluidic system with sample-in-answer-out capability for sensitive, specific, and rapid viral nucleic acid testing. The release of nucleic acids and the subsequent reverse transcription loop-mediated isothermal amplification (RT-LAMP) were integrated into the reaction units of a microfluidic disc. The whole processing steps such as injection of reagents, fluid actuation by rotation, heating and temperature control, and detection of fluorescence signals were carried out automatically by a customized instrument. We validate the centrifugal microfluidic system using oropharyngeal swab samples spiked with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) armored RNA particles. The estimated limit of detection for armored RNA particles is 2 copies per reaction, the throughput is 21 reactions per disc, and the assay sample-to-answer time is approximately 70 min. This enclosed and automated microfluidic system efficiently avoids viral contamination of aerosol, and can be readily adapted for virus detection outside the diagnostic laboratory. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s11426-020-9800-6 and is accessible for authorized users.
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spelling pubmed-73878822020-07-29 A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing Tian, Fei Liu, Chao Deng, Jinqi Han, Ziwei Zhang, Lu Chen, Qinghua Sun, Jiashu Sci China Chem Articles The outbreak of virus-induced infectious diseases poses a global public-health challenge. Nucleic acid amplification testing (NAAT) enables early detection of pandemic viruses and plays a vital role in preventing onward transmission. However, the requirement of skilled operators, expensive instrumentation, and biosafety laboratories has hindered the use of NAAT for screening and diagnosis of suspected patients. Here we report development of a fully automated centrifugal microfluidic system with sample-in-answer-out capability for sensitive, specific, and rapid viral nucleic acid testing. The release of nucleic acids and the subsequent reverse transcription loop-mediated isothermal amplification (RT-LAMP) were integrated into the reaction units of a microfluidic disc. The whole processing steps such as injection of reagents, fluid actuation by rotation, heating and temperature control, and detection of fluorescence signals were carried out automatically by a customized instrument. We validate the centrifugal microfluidic system using oropharyngeal swab samples spiked with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) armored RNA particles. The estimated limit of detection for armored RNA particles is 2 copies per reaction, the throughput is 21 reactions per disc, and the assay sample-to-answer time is approximately 70 min. This enclosed and automated microfluidic system efficiently avoids viral contamination of aerosol, and can be readily adapted for virus detection outside the diagnostic laboratory. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s11426-020-9800-6 and is accessible for authorized users. Science China Press 2020-07-27 2020 /pmc/articles/PMC7387882/ /pubmed/32837510 http://dx.doi.org/10.1007/s11426-020-9800-6 Text en © Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Articles
Tian, Fei
Liu, Chao
Deng, Jinqi
Han, Ziwei
Zhang, Lu
Chen, Qinghua
Sun, Jiashu
A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title_full A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title_fullStr A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title_full_unstemmed A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title_short A fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
title_sort fully automated centrifugal microfluidic system for sample-to-answer viral nucleic acid testing
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387882/
https://www.ncbi.nlm.nih.gov/pubmed/32837510
http://dx.doi.org/10.1007/s11426-020-9800-6
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