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Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit
Nucleic acid testing technology has made considerable progress in the last few years. However, there are still many challenges in the clinical application of multiple nucleic acid assays, such as how to ensure accurate results, increase speed and decrease cost. Herein, a three-way junction structure...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019429/ https://www.ncbi.nlm.nih.gov/pubmed/36928726 http://dx.doi.org/10.1007/s00216-023-04637-3 |
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author | Yu, Chunxu Zhou, Siyan Zhao, Xin Tang, Yidan Wang, Lina Lu, Baiyang Meng, Fanzheng Li, Bingling |
author_facet | Yu, Chunxu Zhou, Siyan Zhao, Xin Tang, Yidan Wang, Lina Lu, Baiyang Meng, Fanzheng Li, Bingling |
author_sort | Yu, Chunxu |
collection | PubMed |
description | Nucleic acid testing technology has made considerable progress in the last few years. However, there are still many challenges in the clinical application of multiple nucleic acid assays, such as how to ensure accurate results, increase speed and decrease cost. Herein, a three-way junction structure has been introduced to specifically translate analytes of loop-mediated isothermal amplification to a catalytic hairpin assembly. For different analyses, a well-optimized nucleic acid circuit can be directly applied to detection, through only one-component replacement, which only not avoids duplicate sequence design but also saves detection cost. Thanks to this design, multiple and logical analysis can be easily realized in a single reaction with ultra-high sensitivity and selectivity. In this paper, Mycoplasma pneumoniae and Streptococcus pneumoniae can be clearly distinguished from the clinical mixed sample with negative control or one analyte in one tube single fluorescence channel. The fair experimental results of actual clinical samples provide a strong support for the possibility of clinical application of this methodology. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04637-3. |
format | Online Article Text |
id | pubmed-10019429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100194292023-03-16 Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit Yu, Chunxu Zhou, Siyan Zhao, Xin Tang, Yidan Wang, Lina Lu, Baiyang Meng, Fanzheng Li, Bingling Anal Bioanal Chem Paper in Forefront Nucleic acid testing technology has made considerable progress in the last few years. However, there are still many challenges in the clinical application of multiple nucleic acid assays, such as how to ensure accurate results, increase speed and decrease cost. Herein, a three-way junction structure has been introduced to specifically translate analytes of loop-mediated isothermal amplification to a catalytic hairpin assembly. For different analyses, a well-optimized nucleic acid circuit can be directly applied to detection, through only one-component replacement, which only not avoids duplicate sequence design but also saves detection cost. Thanks to this design, multiple and logical analysis can be easily realized in a single reaction with ultra-high sensitivity and selectivity. In this paper, Mycoplasma pneumoniae and Streptococcus pneumoniae can be clearly distinguished from the clinical mixed sample with negative control or one analyte in one tube single fluorescence channel. The fair experimental results of actual clinical samples provide a strong support for the possibility of clinical application of this methodology. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-023-04637-3. Springer Berlin Heidelberg 2023-03-16 2023 /pmc/articles/PMC10019429/ /pubmed/36928726 http://dx.doi.org/10.1007/s00216-023-04637-3 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 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 Yu, Chunxu Zhou, Siyan Zhao, Xin Tang, Yidan Wang, Lina Lu, Baiyang Meng, Fanzheng Li, Bingling Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title | Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title_full | Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title_fullStr | Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title_full_unstemmed | Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title_short | Multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
title_sort | multiplex detection of clinical pathogen nucleic acids via a three-way junction structure-based nucleic acid circuit |
topic | Paper in Forefront |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019429/ https://www.ncbi.nlm.nih.gov/pubmed/36928726 http://dx.doi.org/10.1007/s00216-023-04637-3 |
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