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On-chip analysis of respiratory viruses from nasopharyngeal samples
Point-of-care (PoC) testing followed by personalized efficient therapy of infectious diseases may result in a considerable reduction of associated health care costs. Lab-on-a-chip (LoC) systems represent a potentially high efficient class of PoC tools. Here, we present a LoC system for automated pat...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087868/ https://www.ncbi.nlm.nih.gov/pubmed/21603962 http://dx.doi.org/10.1007/s10544-011-9552-4 |
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author | Ritzi-Lehnert, Marion Himmelreich, Ralf Attig, Hans Claußen, Jan Dahlke, Rainer Großhauser, Gerd Holzer, Eva Jeziorski, Markus Schaeffer, Eva Wende, Andy Werner, Sabine Wiborg, Jens Ole Wick, Isabell Drese, Klaus Stefan Rothmann, Thomas |
author_facet | Ritzi-Lehnert, Marion Himmelreich, Ralf Attig, Hans Claußen, Jan Dahlke, Rainer Großhauser, Gerd Holzer, Eva Jeziorski, Markus Schaeffer, Eva Wende, Andy Werner, Sabine Wiborg, Jens Ole Wick, Isabell Drese, Klaus Stefan Rothmann, Thomas |
author_sort | Ritzi-Lehnert, Marion |
collection | PubMed |
description | Point-of-care (PoC) testing followed by personalized efficient therapy of infectious diseases may result in a considerable reduction of associated health care costs. Lab-on-a-chip (LoC) systems represent a potentially high efficient class of PoC tools. Here, we present a LoC system for automated pathogen analysis of respiratory viruses from nasopharyngeal specimens. The device prepares total nucleic acids from extracted swab samples using magnetic silica beads. After reverse transcription the co-purified viral RNA is amplified in accordance with the QIAplex multiplex PCR technology. Hybridized to corresponding QIAGEN LiquiChip beads and labelled with streptavidin R-phycoerythrin, the amplified target sequences are finally detected using a QIAGEN LiquiChip200 workstation. All chemicals needed are either stored freeze-dried on the disposable chip or are provided in liquid form in a reagent cartridge for up to 24 runs. Magnetic stir bars for mixing as well as turning valves with metering structures are integrated into the injection-moulded disposable chip. The core of the controlling instrument is a rotating heating bar construction providing fixed temperatures for fast cycling. PCR times of about half an hour (for 30 cycles) could be achieved for 120 μl reactions, making this system the fastest currently available high-volume PCR chip. The functionality of the system was shown by comparing automatically processed nasopharyngeal samples to ones processed manually according to the QIAGEN “ResPlex™ II Panel v2.0” respiratory virus detection kit. A prototype of the present instrument revealed slightly weaker signal intensities with a similar sensitivity in comparison to the commercially available kit and automated nucleic acid preparation devices, even without protocol optimization. |
format | Online Article Text |
id | pubmed-7087868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70878682020-03-23 On-chip analysis of respiratory viruses from nasopharyngeal samples Ritzi-Lehnert, Marion Himmelreich, Ralf Attig, Hans Claußen, Jan Dahlke, Rainer Großhauser, Gerd Holzer, Eva Jeziorski, Markus Schaeffer, Eva Wende, Andy Werner, Sabine Wiborg, Jens Ole Wick, Isabell Drese, Klaus Stefan Rothmann, Thomas Biomed Microdevices Article Point-of-care (PoC) testing followed by personalized efficient therapy of infectious diseases may result in a considerable reduction of associated health care costs. Lab-on-a-chip (LoC) systems represent a potentially high efficient class of PoC tools. Here, we present a LoC system for automated pathogen analysis of respiratory viruses from nasopharyngeal specimens. The device prepares total nucleic acids from extracted swab samples using magnetic silica beads. After reverse transcription the co-purified viral RNA is amplified in accordance with the QIAplex multiplex PCR technology. Hybridized to corresponding QIAGEN LiquiChip beads and labelled with streptavidin R-phycoerythrin, the amplified target sequences are finally detected using a QIAGEN LiquiChip200 workstation. All chemicals needed are either stored freeze-dried on the disposable chip or are provided in liquid form in a reagent cartridge for up to 24 runs. Magnetic stir bars for mixing as well as turning valves with metering structures are integrated into the injection-moulded disposable chip. The core of the controlling instrument is a rotating heating bar construction providing fixed temperatures for fast cycling. PCR times of about half an hour (for 30 cycles) could be achieved for 120 μl reactions, making this system the fastest currently available high-volume PCR chip. The functionality of the system was shown by comparing automatically processed nasopharyngeal samples to ones processed manually according to the QIAGEN “ResPlex™ II Panel v2.0” respiratory virus detection kit. A prototype of the present instrument revealed slightly weaker signal intensities with a similar sensitivity in comparison to the commercially available kit and automated nucleic acid preparation devices, even without protocol optimization. Springer US 2011-05-21 2011 /pmc/articles/PMC7087868/ /pubmed/21603962 http://dx.doi.org/10.1007/s10544-011-9552-4 Text en © Springer Science+Business Media, LLC 2011 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 | Article Ritzi-Lehnert, Marion Himmelreich, Ralf Attig, Hans Claußen, Jan Dahlke, Rainer Großhauser, Gerd Holzer, Eva Jeziorski, Markus Schaeffer, Eva Wende, Andy Werner, Sabine Wiborg, Jens Ole Wick, Isabell Drese, Klaus Stefan Rothmann, Thomas On-chip analysis of respiratory viruses from nasopharyngeal samples |
title | On-chip analysis of respiratory viruses from nasopharyngeal samples |
title_full | On-chip analysis of respiratory viruses from nasopharyngeal samples |
title_fullStr | On-chip analysis of respiratory viruses from nasopharyngeal samples |
title_full_unstemmed | On-chip analysis of respiratory viruses from nasopharyngeal samples |
title_short | On-chip analysis of respiratory viruses from nasopharyngeal samples |
title_sort | on-chip analysis of respiratory viruses from nasopharyngeal samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087868/ https://www.ncbi.nlm.nih.gov/pubmed/21603962 http://dx.doi.org/10.1007/s10544-011-9552-4 |
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