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Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens

Background: Antigen detection assays and viral isolation techniques are routinely used to detect adenoviruses (Ad) associated with respiratory infections, and the value of the polymerase chain reaction (PCR) has recently been assessed. Objectives: This paper describes a PCR-hybridization-immunoenzym...

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Autores principales: Vabret, Astrid, Gouarin, Stéphanie, Joannes, Martine, Barranger, Come, Petitjean, Joëlle, Corbet, Sandrine, Brouard, Jacques, Lafay, Françoise, Duhamel, Jean-François, Guillois, Bernard, Freymuth, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129058/
https://www.ncbi.nlm.nih.gov/pubmed/15364267
http://dx.doi.org/10.1016/j.jcv.2004.04.003
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author Vabret, Astrid
Gouarin, Stéphanie
Joannes, Martine
Barranger, Come
Petitjean, Joëlle
Corbet, Sandrine
Brouard, Jacques
Lafay, Françoise
Duhamel, Jean-François
Guillois, Bernard
Freymuth, François
author_facet Vabret, Astrid
Gouarin, Stéphanie
Joannes, Martine
Barranger, Come
Petitjean, Joëlle
Corbet, Sandrine
Brouard, Jacques
Lafay, Françoise
Duhamel, Jean-François
Guillois, Bernard
Freymuth, François
author_sort Vabret, Astrid
collection PubMed
description Background: Antigen detection assays and viral isolation techniques are routinely used to detect adenoviruses (Ad) associated with respiratory infections, and the value of the polymerase chain reaction (PCR) has recently been assessed. Objectives: This paper describes a PCR-hybridization-immunoenzymatic assay (PCR Adenovirus consensus(®)) used to detect Ad and identify Ad species in respiratory specimens. Results: On seven representative serotypes Ad 12, Ad 3, Ad 7, Ad 11, Ad 1, Ad 8, Ad 4, the mean genome equivalents per ml and the mean 50% infectious doses per ml were 10(6.3)and 10(4), respectively. Using 362 nasal aspirates from children, Ad were detected by immunofluorescence (IF) and culture in 97 cases (27%), by the PCR-Ad hexon method in 107 cases (29.5%) and by the PCR Adenovirus Consensus(®) method in 113 cases (31.2%); 13 samples were found positive by both PCR and negative by the IF and culture methods; five samples were only positive according to the PCR Adenovirus Consensus(®) method. The sensitivity, specificity, predictive positive value and predictive negative value of the PCR Adenovirus Consensus(®) method were 97.9%, 93.2%, 84%, 99.1%, respectively. The method identified the species (sp) from 91 positive amplicons: 1 Ad sp A, 44 Ad sp B, 42 Ad sp C, 3 Ad sp E, and 1 Ad sp F; 85 isolates were identified by IF or the neutralisation in culture, and 86 by a PCR-RE digestion method. The PCR Adenovirus Consensus(®) detected six positive samples that were negative according to the IF and culture methods, and it identified the precise species of nine IF-positive and culture-negative nasal aspirates. Conclusion: The PCR Adenovirus Consensus(®) technique is more efficient than the classical IF or culture techniques for the detection of Ad in respiratory samples. An internal control is included to validate the screening results, and specific probes are used to identify the Ad species.
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spelling pubmed-71290582020-04-08 Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens Vabret, Astrid Gouarin, Stéphanie Joannes, Martine Barranger, Come Petitjean, Joëlle Corbet, Sandrine Brouard, Jacques Lafay, Françoise Duhamel, Jean-François Guillois, Bernard Freymuth, François J Clin Virol Article Background: Antigen detection assays and viral isolation techniques are routinely used to detect adenoviruses (Ad) associated with respiratory infections, and the value of the polymerase chain reaction (PCR) has recently been assessed. Objectives: This paper describes a PCR-hybridization-immunoenzymatic assay (PCR Adenovirus consensus(®)) used to detect Ad and identify Ad species in respiratory specimens. Results: On seven representative serotypes Ad 12, Ad 3, Ad 7, Ad 11, Ad 1, Ad 8, Ad 4, the mean genome equivalents per ml and the mean 50% infectious doses per ml were 10(6.3)and 10(4), respectively. Using 362 nasal aspirates from children, Ad were detected by immunofluorescence (IF) and culture in 97 cases (27%), by the PCR-Ad hexon method in 107 cases (29.5%) and by the PCR Adenovirus Consensus(®) method in 113 cases (31.2%); 13 samples were found positive by both PCR and negative by the IF and culture methods; five samples were only positive according to the PCR Adenovirus Consensus(®) method. The sensitivity, specificity, predictive positive value and predictive negative value of the PCR Adenovirus Consensus(®) method were 97.9%, 93.2%, 84%, 99.1%, respectively. The method identified the species (sp) from 91 positive amplicons: 1 Ad sp A, 44 Ad sp B, 42 Ad sp C, 3 Ad sp E, and 1 Ad sp F; 85 isolates were identified by IF or the neutralisation in culture, and 86 by a PCR-RE digestion method. The PCR Adenovirus Consensus(®) detected six positive samples that were negative according to the IF and culture methods, and it identified the precise species of nine IF-positive and culture-negative nasal aspirates. Conclusion: The PCR Adenovirus Consensus(®) technique is more efficient than the classical IF or culture techniques for the detection of Ad in respiratory samples. An internal control is included to validate the screening results, and specific probes are used to identify the Ad species. Elsevier B.V. 2004-10 2004-07-07 /pmc/articles/PMC7129058/ /pubmed/15364267 http://dx.doi.org/10.1016/j.jcv.2004.04.003 Text en Copyright © 2004 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
Vabret, Astrid
Gouarin, Stéphanie
Joannes, Martine
Barranger, Come
Petitjean, Joëlle
Corbet, Sandrine
Brouard, Jacques
Lafay, Françoise
Duhamel, Jean-François
Guillois, Bernard
Freymuth, François
Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title_full Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title_fullStr Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title_full_unstemmed Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title_short Development of a PCR-and hybridization-based assay (PCR Adenovirus Consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
title_sort development of a pcr-and hybridization-based assay (pcr adenovirus consensus(®)) for the detection and the species identification of adenoviruses in respiratory specimens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129058/
https://www.ncbi.nlm.nih.gov/pubmed/15364267
http://dx.doi.org/10.1016/j.jcv.2004.04.003
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