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Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens

Rapid and accurate detection and identification of viruses causing respiratory tract infections is important for patient care and disease control. Despite the fact that several assays are available, identification of an etiological agent is not possible in ∼30% of patients suffering from respiratory...

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Autores principales: Pyrc, Krzysztof, Stożek, Karol, Wojcik, Krzysztof, Gawron, Katarzyna, Zeglen, Slawomir, Karolak, Wojciech, Wojarski, Jacek, Ochman, Marek, Hubalewska-Mazgaj, Magdalena, Bochenek, Grazyna, Sanak, Marek, Zembala, Marian, Szczeklik, Andrzej, Potempa, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293820/
https://www.ncbi.nlm.nih.gov/pubmed/22403676
http://dx.doi.org/10.1371/journal.pone.0032582
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author Pyrc, Krzysztof
Stożek, Karol
Wojcik, Krzysztof
Gawron, Katarzyna
Zeglen, Slawomir
Karolak, Wojciech
Wojarski, Jacek
Ochman, Marek
Hubalewska-Mazgaj, Magdalena
Bochenek, Grazyna
Sanak, Marek
Zembala, Marian
Szczeklik, Andrzej
Potempa, Jan
author_facet Pyrc, Krzysztof
Stożek, Karol
Wojcik, Krzysztof
Gawron, Katarzyna
Zeglen, Slawomir
Karolak, Wojciech
Wojarski, Jacek
Ochman, Marek
Hubalewska-Mazgaj, Magdalena
Bochenek, Grazyna
Sanak, Marek
Zembala, Marian
Szczeklik, Andrzej
Potempa, Jan
author_sort Pyrc, Krzysztof
collection PubMed
description Rapid and accurate detection and identification of viruses causing respiratory tract infections is important for patient care and disease control. Despite the fact that several assays are available, identification of an etiological agent is not possible in ∼30% of patients suffering from respiratory tract diseases. Therefore, the aim of the current study was to develop a diagnostic set for the detection of respiratory viruses with sensitivity as low as 1–10 copies per reaction. Evaluation of the assay using a training clinical sample set showed that viral nucleic acids were identified in ∼76% of cases. To improve assay performance and facilitate the identification of novel species or emerging strains, cultures of fully differentiated human airway epithelium were used to pre-amplify infectious viruses. This additional step resulted in the detection of pathogens in all samples tested. Based on these results it can be hypothesized that the lack of an etiological agent in some clinical samples, both reported previously and observed in the present study, may result not only from the presence of unknown viral species, but also from imperfections in the detection methods used.
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spelling pubmed-32938202012-03-08 Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens Pyrc, Krzysztof Stożek, Karol Wojcik, Krzysztof Gawron, Katarzyna Zeglen, Slawomir Karolak, Wojciech Wojarski, Jacek Ochman, Marek Hubalewska-Mazgaj, Magdalena Bochenek, Grazyna Sanak, Marek Zembala, Marian Szczeklik, Andrzej Potempa, Jan PLoS One Research Article Rapid and accurate detection and identification of viruses causing respiratory tract infections is important for patient care and disease control. Despite the fact that several assays are available, identification of an etiological agent is not possible in ∼30% of patients suffering from respiratory tract diseases. Therefore, the aim of the current study was to develop a diagnostic set for the detection of respiratory viruses with sensitivity as low as 1–10 copies per reaction. Evaluation of the assay using a training clinical sample set showed that viral nucleic acids were identified in ∼76% of cases. To improve assay performance and facilitate the identification of novel species or emerging strains, cultures of fully differentiated human airway epithelium were used to pre-amplify infectious viruses. This additional step resulted in the detection of pathogens in all samples tested. Based on these results it can be hypothesized that the lack of an etiological agent in some clinical samples, both reported previously and observed in the present study, may result not only from the presence of unknown viral species, but also from imperfections in the detection methods used. Public Library of Science 2012-03-05 /pmc/articles/PMC3293820/ /pubmed/22403676 http://dx.doi.org/10.1371/journal.pone.0032582 Text en Pyrc et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pyrc, Krzysztof
Stożek, Karol
Wojcik, Krzysztof
Gawron, Katarzyna
Zeglen, Slawomir
Karolak, Wojciech
Wojarski, Jacek
Ochman, Marek
Hubalewska-Mazgaj, Magdalena
Bochenek, Grazyna
Sanak, Marek
Zembala, Marian
Szczeklik, Andrzej
Potempa, Jan
Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title_full Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title_fullStr Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title_full_unstemmed Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title_short Use of Sensitive, Broad-Spectrum Molecular Assays and Human Airway Epithelium Cultures for Detection of Respiratory Pathogens
title_sort use of sensitive, broad-spectrum molecular assays and human airway epithelium cultures for detection of respiratory pathogens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293820/
https://www.ncbi.nlm.nih.gov/pubmed/22403676
http://dx.doi.org/10.1371/journal.pone.0032582
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