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A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens

Rapid and accurate identification of respiratory tract infection pathogens is of utmost importance for clinical diagnosis and treatment, as well as prevention of pathogen transmission. To meet this demand, a microfluidic chip-based PCR-array system, Onestart, was developed. The Onestart system uses...

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Autores principales: Huang, Enqi, Wang, Yu, Yang, Na, Shu, Bowen, Zhang, Guohao, Liu, Dayu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829496/
https://www.ncbi.nlm.nih.gov/pubmed/33492406
http://dx.doi.org/10.1007/s00216-021-03171-4
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author Huang, Enqi
Wang, Yu
Yang, Na
Shu, Bowen
Zhang, Guohao
Liu, Dayu
author_facet Huang, Enqi
Wang, Yu
Yang, Na
Shu, Bowen
Zhang, Guohao
Liu, Dayu
author_sort Huang, Enqi
collection PubMed
description Rapid and accurate identification of respiratory tract infection pathogens is of utmost importance for clinical diagnosis and treatment, as well as prevention of pathogen transmission. To meet this demand, a microfluidic chip-based PCR-array system, Onestart, was developed. The Onestart system uses a microfluidic chip packaged with all the reagents required, and the waste liquid is also collected and stored on the chip. This ready-to-use system can complete the detection of 21 pathogens in a fully integrated manner, with sample lysis, nucleic acid extraction/purification, and real-time PCR sequentially implemented on the same chip. The entire analysis process is completed within 1.5 h, and the system automatically generates a test report. The lower limit-of-detection (LOD) of the Onestart assay was determined to be 1.0 × 10(3) copies·mL(−1). The inter-batch variation of cycle threshold (Ct) values ranged from 0.08% to 0.69%, and the intra-batch variation ranged from 0.9% to 2.66%. Analytical results of the reference sample mix showed a 100% specificity of the Onestart assay. The analysis of batched clinical samples showed consistency of the Onestart assay with real-time PCR. With its ability to provide rapid, sensitive, and specific detection of respiratory tract infection pathogens, application of the Onestart system will facilitate timely clinical management of respiratory tract infections and effective prevention of pathogen transmission. GRAPHICAL ABSTRACT: [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03171-4.
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spelling pubmed-78294962021-01-25 A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens Huang, Enqi Wang, Yu Yang, Na Shu, Bowen Zhang, Guohao Liu, Dayu Anal Bioanal Chem Paper in Forefront Rapid and accurate identification of respiratory tract infection pathogens is of utmost importance for clinical diagnosis and treatment, as well as prevention of pathogen transmission. To meet this demand, a microfluidic chip-based PCR-array system, Onestart, was developed. The Onestart system uses a microfluidic chip packaged with all the reagents required, and the waste liquid is also collected and stored on the chip. This ready-to-use system can complete the detection of 21 pathogens in a fully integrated manner, with sample lysis, nucleic acid extraction/purification, and real-time PCR sequentially implemented on the same chip. The entire analysis process is completed within 1.5 h, and the system automatically generates a test report. The lower limit-of-detection (LOD) of the Onestart assay was determined to be 1.0 × 10(3) copies·mL(−1). The inter-batch variation of cycle threshold (Ct) values ranged from 0.08% to 0.69%, and the intra-batch variation ranged from 0.9% to 2.66%. Analytical results of the reference sample mix showed a 100% specificity of the Onestart assay. The analysis of batched clinical samples showed consistency of the Onestart assay with real-time PCR. With its ability to provide rapid, sensitive, and specific detection of respiratory tract infection pathogens, application of the Onestart system will facilitate timely clinical management of respiratory tract infections and effective prevention of pathogen transmission. GRAPHICAL ABSTRACT: [Figure: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-021-03171-4. Springer Berlin Heidelberg 2021-01-25 2021 /pmc/articles/PMC7829496/ /pubmed/33492406 http://dx.doi.org/10.1007/s00216-021-03171-4 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 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 Paper in Forefront
Huang, Enqi
Wang, Yu
Yang, Na
Shu, Bowen
Zhang, Guohao
Liu, Dayu
A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title_full A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title_fullStr A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title_full_unstemmed A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title_short A fully automated microfluidic PCR-array system for rapid detection of multiple respiratory tract infection pathogens
title_sort fully automated microfluidic pcr-array system for rapid detection of multiple respiratory tract infection pathogens
topic Paper in Forefront
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7829496/
https://www.ncbi.nlm.nih.gov/pubmed/33492406
http://dx.doi.org/10.1007/s00216-021-03171-4
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