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Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis

Invasive pulmonary aspergillosis (IPA) is a common complication of immunosuppression. Rapid diagnosis using molecular techniques is essential to improve patient survival. PCR techniques are promising in enhancing Aspergillus detection in blood and respiratory samples. We evaluate for the first time...

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Autores principales: Denis, Julie, Forouzanfar, Faezeh, Herbrecht, Raoul, Toussaint, Elise, Kessler, Romain, Sabou, Marcela, Candolfi, Ermanno, Letsher-Bru, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185652/
https://www.ncbi.nlm.nih.gov/pubmed/29471112
http://dx.doi.org/10.1016/j.jmoldx.2017.12.005
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author Denis, Julie
Forouzanfar, Faezeh
Herbrecht, Raoul
Toussaint, Elise
Kessler, Romain
Sabou, Marcela
Candolfi, Ermanno
Letsher-Bru, Valérie
author_facet Denis, Julie
Forouzanfar, Faezeh
Herbrecht, Raoul
Toussaint, Elise
Kessler, Romain
Sabou, Marcela
Candolfi, Ermanno
Letsher-Bru, Valérie
author_sort Denis, Julie
collection PubMed
description Invasive pulmonary aspergillosis (IPA) is a common complication of immunosuppression. Rapid diagnosis using molecular techniques is essential to improve patient survival. PCR techniques are promising in enhancing Aspergillus detection in blood and respiratory samples. We evaluate for the first time the performances of two commercial real-time PCR kits, the A. fumigatus Bio-Evolution and the MycoGENIE A. fumigatus for the detection of A. fumigatus DNA in bronchoalveolar lavage (BAL) from patients with and without IPA. Seventy-three BAL samples were included. Thirty-one of them corresponded to patients with probable IPA, 11 to patients with possible IPA, and 31 to patients without aspergillosis, according to the 2008 European Organization for Research and Treatment of Cancer/Mycoses Study Group criteria. In the probable IPA group, A. fumigatus Bio-Evolution and the MycoGENIE A. fumigatus real-time PCR kits showed a specificity of 100% and a sensitivity of 81% and 71%, respectively. The A. fumigatus Bio-Evolution detected Aspergillus DNA in the 14 BAL samples with a positive Aspergillus culture result, whereas the MycoGENIE A. fumigatus PCR result was positive only for 12. In the possible IPA group, there were no positive real-time PCR or positive Aspergillus culture results. For the patients without aspergillosis, no positive result was observed for real-time PCR kit, despite the presence of various other non-Aspergillus pathogens in this group. Our study demonstrates an excellent specificity and a good sensitivity of A. fumigatus DNA detection in BAL samples with both kits.
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spelling pubmed-71856522020-04-28 Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis Denis, Julie Forouzanfar, Faezeh Herbrecht, Raoul Toussaint, Elise Kessler, Romain Sabou, Marcela Candolfi, Ermanno Letsher-Bru, Valérie J Mol Diagn Regular Article Invasive pulmonary aspergillosis (IPA) is a common complication of immunosuppression. Rapid diagnosis using molecular techniques is essential to improve patient survival. PCR techniques are promising in enhancing Aspergillus detection in blood and respiratory samples. We evaluate for the first time the performances of two commercial real-time PCR kits, the A. fumigatus Bio-Evolution and the MycoGENIE A. fumigatus for the detection of A. fumigatus DNA in bronchoalveolar lavage (BAL) from patients with and without IPA. Seventy-three BAL samples were included. Thirty-one of them corresponded to patients with probable IPA, 11 to patients with possible IPA, and 31 to patients without aspergillosis, according to the 2008 European Organization for Research and Treatment of Cancer/Mycoses Study Group criteria. In the probable IPA group, A. fumigatus Bio-Evolution and the MycoGENIE A. fumigatus real-time PCR kits showed a specificity of 100% and a sensitivity of 81% and 71%, respectively. The A. fumigatus Bio-Evolution detected Aspergillus DNA in the 14 BAL samples with a positive Aspergillus culture result, whereas the MycoGENIE A. fumigatus PCR result was positive only for 12. In the possible IPA group, there were no positive real-time PCR or positive Aspergillus culture results. For the patients without aspergillosis, no positive result was observed for real-time PCR kit, despite the presence of various other non-Aspergillus pathogens in this group. Our study demonstrates an excellent specificity and a good sensitivity of A. fumigatus DNA detection in BAL samples with both kits. American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. 2018-05 2018-02-19 /pmc/articles/PMC7185652/ /pubmed/29471112 http://dx.doi.org/10.1016/j.jmoldx.2017.12.005 Text en © 2018 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. 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 Regular Article
Denis, Julie
Forouzanfar, Faezeh
Herbrecht, Raoul
Toussaint, Elise
Kessler, Romain
Sabou, Marcela
Candolfi, Ermanno
Letsher-Bru, Valérie
Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title_full Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title_fullStr Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title_full_unstemmed Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title_short Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis
title_sort evaluation of two commercial real-time pcr kits for aspergillus dna detection in bronchoalveolar lavage fluid in patients with invasive pulmonary aspergillosis
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185652/
https://www.ncbi.nlm.nih.gov/pubmed/29471112
http://dx.doi.org/10.1016/j.jmoldx.2017.12.005
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