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Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children
BACKGROUND: Polymerase chain reaction (PCR) is a sensitive tool for detection of respiratory picornaviruses. However, the clinical relevance of picornavirus detection by PCR is unclear. Immunofluorescence (IF), widely used to detect other respiratory viruses, has recently been introduced as a promis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172693/ https://www.ncbi.nlm.nih.gov/pubmed/20471907 http://dx.doi.org/10.1016/j.jcv.2010.04.005 |
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author | Schindera, Christina Kraemer, Ann Lea Regamey, Nicolas Aebi, Christoph Gorgievski-Hrisoho, Meri Barbani, Maria Teresa |
author_facet | Schindera, Christina Kraemer, Ann Lea Regamey, Nicolas Aebi, Christoph Gorgievski-Hrisoho, Meri Barbani, Maria Teresa |
author_sort | Schindera, Christina |
collection | PubMed |
description | BACKGROUND: Polymerase chain reaction (PCR) is a sensitive tool for detection of respiratory picornaviruses. However, the clinical relevance of picornavirus detection by PCR is unclear. Immunofluorescence (IF), widely used to detect other respiratory viruses, has recently been introduced as a promising detection method for respiratory picornaviruses. OBJECTIVES: To compare the clinical manifestations of respiratory picornavirus infections detected by IF with those of respiratory picornavirus infections detected by xTAG multiplex PCR in hospitalized children. STUDY DESIGN: During a 1-year period, nasopharyngeal aspirates (NPA) from all children hospitalized due to an acute respiratory infection were prospectively analyzed by IF. All respiratory picornavirus positive IF samples and 100 IF negative samples were further tested with xTAG multiplex PCR. After exclusion of children with co-morbidities and viral co-infections, monoinfections with respiratory picornaviruses were detected in 108 NPA of 108 otherwise healthy children by IF and/or PCR. We compared group 1 children (IF and PCR positive, n = 84) with group 2 children (IF negative and PCR positive, n = 24) with regard to clinical manifestations of the infection. RESULTS: Wheezy bronchitis was diagnosed more often in group 1 than in group 2 (71% vs. 46%, p = 0.028). In contrast, group 2 patients were diagnosed more frequently with pneumonia (17% vs. 6%, p = 0.014) accompanied by higher levels of C-reactive protein (46 mg/l vs. 11 mg/l, p = 0.009). CONCLUSIONS: Picornavirus detection by IF in children with acute respiratory infection is associated with the clinical presentation of wheezy bronchitis. The finding of a more frequent diagnosis of pneumonia in picornavirus PCR positive but IF negative children warrants further investigation. |
format | Online Article Text |
id | pubmed-7172693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71726932020-04-22 Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children Schindera, Christina Kraemer, Ann Lea Regamey, Nicolas Aebi, Christoph Gorgievski-Hrisoho, Meri Barbani, Maria Teresa J Clin Virol Article BACKGROUND: Polymerase chain reaction (PCR) is a sensitive tool for detection of respiratory picornaviruses. However, the clinical relevance of picornavirus detection by PCR is unclear. Immunofluorescence (IF), widely used to detect other respiratory viruses, has recently been introduced as a promising detection method for respiratory picornaviruses. OBJECTIVES: To compare the clinical manifestations of respiratory picornavirus infections detected by IF with those of respiratory picornavirus infections detected by xTAG multiplex PCR in hospitalized children. STUDY DESIGN: During a 1-year period, nasopharyngeal aspirates (NPA) from all children hospitalized due to an acute respiratory infection were prospectively analyzed by IF. All respiratory picornavirus positive IF samples and 100 IF negative samples were further tested with xTAG multiplex PCR. After exclusion of children with co-morbidities and viral co-infections, monoinfections with respiratory picornaviruses were detected in 108 NPA of 108 otherwise healthy children by IF and/or PCR. We compared group 1 children (IF and PCR positive, n = 84) with group 2 children (IF negative and PCR positive, n = 24) with regard to clinical manifestations of the infection. RESULTS: Wheezy bronchitis was diagnosed more often in group 1 than in group 2 (71% vs. 46%, p = 0.028). In contrast, group 2 patients were diagnosed more frequently with pneumonia (17% vs. 6%, p = 0.014) accompanied by higher levels of C-reactive protein (46 mg/l vs. 11 mg/l, p = 0.009). CONCLUSIONS: Picornavirus detection by IF in children with acute respiratory infection is associated with the clinical presentation of wheezy bronchitis. The finding of a more frequent diagnosis of pneumonia in picornavirus PCR positive but IF negative children warrants further investigation. Elsevier B.V. 2010-07 2010-05-14 /pmc/articles/PMC7172693/ /pubmed/20471907 http://dx.doi.org/10.1016/j.jcv.2010.04.005 Text en Copyright © 2010 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Schindera, Christina Kraemer, Ann Lea Regamey, Nicolas Aebi, Christoph Gorgievski-Hrisoho, Meri Barbani, Maria Teresa Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title | Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title_full | Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title_fullStr | Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title_full_unstemmed | Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title_short | Immunofluorescence versus xTAG multiplex PCR for the detection of respiratory picornavirus infections in children |
title_sort | immunofluorescence versus xtag multiplex pcr for the detection of respiratory picornavirus infections in children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172693/ https://www.ncbi.nlm.nih.gov/pubmed/20471907 http://dx.doi.org/10.1016/j.jcv.2010.04.005 |
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