Cargando…

Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10

The aim of this study was to determine the prevalence of respiratory viruses and to prospectively evaluate the performance of the fast-track diagnostics (FTD) respiratory pathogens multiplex PCR assay shortly after the 2009/10 influenza pandemic. Highly sensitive monoplex real-time PCR assays served...

Descripción completa

Detalles Bibliográficos
Autores principales: Bierbaum, Sibylle, Forster, Johannes, Berner, Reinhard, Rücker, Gerta, Rohde, Gernot, Neumann-Haefelin, Dieter, Panning, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086993/
https://www.ncbi.nlm.nih.gov/pubmed/24126621
http://dx.doi.org/10.1007/s00705-013-1876-3
_version_ 1783509243150729216
author Bierbaum, Sibylle
Forster, Johannes
Berner, Reinhard
Rücker, Gerta
Rohde, Gernot
Neumann-Haefelin, Dieter
Panning, Marcus
author_facet Bierbaum, Sibylle
Forster, Johannes
Berner, Reinhard
Rücker, Gerta
Rohde, Gernot
Neumann-Haefelin, Dieter
Panning, Marcus
author_sort Bierbaum, Sibylle
collection PubMed
description The aim of this study was to determine the prevalence of respiratory viruses and to prospectively evaluate the performance of the fast-track diagnostics (FTD) respiratory pathogens multiplex PCR assay shortly after the 2009/10 influenza pandemic. Highly sensitive monoplex real-time PCR assays served as references. Discrepant results were further analyzed by the xTAG RVP Fast assay. A total of 369 respiratory samples from children and adults were collected prospectively in Germany from December 2009 until June 2010. The sensitivity and specificity of the FTD assay after resolution of discrepant results was 92.2 % and 99.5 %, respectively. Lowest specificity of the FTD assay was observed for human bocavirus. Multiple detections were recorded in 33/369 (8.9 %) of the samples by monoplex PCR and in 43/369 (11.7 %) using the FTD assay. The most prevalent viruses were respiratory syncytial virus and human metapneumovirus. Only pandemic influenza virus A/H1N1 (2009), and not seasonal influenza virus, was detected. Viruses other than influenza virus accounted for the majority of acute respiratory infections. The FTD assay can be easily implemented in general diagnostic laboratories and facilitate the optimization of patient-management schemes.
format Online
Article
Text
id pubmed-7086993
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Springer Vienna
record_format MEDLINE/PubMed
spelling pubmed-70869932020-03-23 Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10 Bierbaum, Sibylle Forster, Johannes Berner, Reinhard Rücker, Gerta Rohde, Gernot Neumann-Haefelin, Dieter Panning, Marcus Arch Virol Original Article The aim of this study was to determine the prevalence of respiratory viruses and to prospectively evaluate the performance of the fast-track diagnostics (FTD) respiratory pathogens multiplex PCR assay shortly after the 2009/10 influenza pandemic. Highly sensitive monoplex real-time PCR assays served as references. Discrepant results were further analyzed by the xTAG RVP Fast assay. A total of 369 respiratory samples from children and adults were collected prospectively in Germany from December 2009 until June 2010. The sensitivity and specificity of the FTD assay after resolution of discrepant results was 92.2 % and 99.5 %, respectively. Lowest specificity of the FTD assay was observed for human bocavirus. Multiple detections were recorded in 33/369 (8.9 %) of the samples by monoplex PCR and in 43/369 (11.7 %) using the FTD assay. The most prevalent viruses were respiratory syncytial virus and human metapneumovirus. Only pandemic influenza virus A/H1N1 (2009), and not seasonal influenza virus, was detected. Viruses other than influenza virus accounted for the majority of acute respiratory infections. The FTD assay can be easily implemented in general diagnostic laboratories and facilitate the optimization of patient-management schemes. Springer Vienna 2013-10-15 2014 /pmc/articles/PMC7086993/ /pubmed/24126621 http://dx.doi.org/10.1007/s00705-013-1876-3 Text en © Springer-Verlag Wien 2013 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 Original Article
Bierbaum, Sibylle
Forster, Johannes
Berner, Reinhard
Rücker, Gerta
Rohde, Gernot
Neumann-Haefelin, Dieter
Panning, Marcus
Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title_full Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title_fullStr Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title_full_unstemmed Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title_short Detection of respiratory viruses using a multiplex real-time PCR assay in Germany, 2009/10
title_sort detection of respiratory viruses using a multiplex real-time pcr assay in germany, 2009/10
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086993/
https://www.ncbi.nlm.nih.gov/pubmed/24126621
http://dx.doi.org/10.1007/s00705-013-1876-3
work_keys_str_mv AT bierbaumsibylle detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT forsterjohannes detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT bernerreinhard detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT ruckergerta detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT rohdegernot detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT neumannhaefelindieter detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT panningmarcus detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910
AT detectionofrespiratoryvirusesusingamultiplexrealtimepcrassayingermany200910