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Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients

This is the first study comparing three commercially available PCR assays for the detection of Aspergillus DNA from respiratory specimen of immunocompromised patients and the presence of cyp51A gene mutations. Bronchoalveolar lavages (BALs, N = 103) from patients with haematological/oncological unde...

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Autores principales: Scharmann, Ulrike, Kirchhoff, Lisa, Hain, Andrea, Buer, Jan, Koldehoff, Michael, Steinmann, Joerg, Rath, Peter-Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916969/
https://www.ncbi.nlm.nih.gov/pubmed/33670173
http://dx.doi.org/10.3390/jof7020132
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author Scharmann, Ulrike
Kirchhoff, Lisa
Hain, Andrea
Buer, Jan
Koldehoff, Michael
Steinmann, Joerg
Rath, Peter-Michael
author_facet Scharmann, Ulrike
Kirchhoff, Lisa
Hain, Andrea
Buer, Jan
Koldehoff, Michael
Steinmann, Joerg
Rath, Peter-Michael
author_sort Scharmann, Ulrike
collection PubMed
description This is the first study comparing three commercially available PCR assays for the detection of Aspergillus DNA from respiratory specimen of immunocompromised patients and the presence of cyp51A gene mutations. Bronchoalveolar lavages (BALs, N = 103) from patients with haematological/oncological underlying diseases were retrospectively investigated. The performance of three PCR assays, namely MycoGENIE(®) Aspergillus fumigatus Real-Time PCR Kit (Adamtech), Fungiplex(®) Aspergillus Azole-R IVD Real-Time PCR Kit (Bruker Daltonik GmbH) and AsperGenius(®) (PathoNostics B.V.), were evaluated. All patients were categorised following current EORTC/MSG criteria, with exclusion of the PCR-results. From the 11 invasive pulmonary aspergillosis (IPA) probable samples, eight were detected with MycoGENIE(®), resulting in a sensitivity of 80% and a specificity of 73%. Furthermore, Fungiplex(®) resulted in six positive BALs with a sensitivity of 60% and a specificity of 91% and AsperGenius(®) in seven positive BAL samples, with a sensitivity of 64% and a specificity of 97%. No proven IPA was detected. One isolate showed phenotypically an azole-resistance, which was also detected in each of the tested PCR assays with the mutation in TR34. The here tested PCR assays were capable of reliably detecting A. fumigatus DNA, as well as differentiation of the common cyp51A gene mutations. However, evaluation on the AsperGenius(®) assay revealed a low risk of false positive results.
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spelling pubmed-79169692021-03-01 Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients Scharmann, Ulrike Kirchhoff, Lisa Hain, Andrea Buer, Jan Koldehoff, Michael Steinmann, Joerg Rath, Peter-Michael J Fungi (Basel) Article This is the first study comparing three commercially available PCR assays for the detection of Aspergillus DNA from respiratory specimen of immunocompromised patients and the presence of cyp51A gene mutations. Bronchoalveolar lavages (BALs, N = 103) from patients with haematological/oncological underlying diseases were retrospectively investigated. The performance of three PCR assays, namely MycoGENIE(®) Aspergillus fumigatus Real-Time PCR Kit (Adamtech), Fungiplex(®) Aspergillus Azole-R IVD Real-Time PCR Kit (Bruker Daltonik GmbH) and AsperGenius(®) (PathoNostics B.V.), were evaluated. All patients were categorised following current EORTC/MSG criteria, with exclusion of the PCR-results. From the 11 invasive pulmonary aspergillosis (IPA) probable samples, eight were detected with MycoGENIE(®), resulting in a sensitivity of 80% and a specificity of 73%. Furthermore, Fungiplex(®) resulted in six positive BALs with a sensitivity of 60% and a specificity of 91% and AsperGenius(®) in seven positive BAL samples, with a sensitivity of 64% and a specificity of 97%. No proven IPA was detected. One isolate showed phenotypically an azole-resistance, which was also detected in each of the tested PCR assays with the mutation in TR34. The here tested PCR assays were capable of reliably detecting A. fumigatus DNA, as well as differentiation of the common cyp51A gene mutations. However, evaluation on the AsperGenius(®) assay revealed a low risk of false positive results. MDPI 2021-02-11 /pmc/articles/PMC7916969/ /pubmed/33670173 http://dx.doi.org/10.3390/jof7020132 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Scharmann, Ulrike
Kirchhoff, Lisa
Hain, Andrea
Buer, Jan
Koldehoff, Michael
Steinmann, Joerg
Rath, Peter-Michael
Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title_full Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title_fullStr Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title_full_unstemmed Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title_short Evaluation of Three Commercial PCR Assays for the Detection of Azole-Resistant Aspergillus fumigatus from Respiratory Samples of Immunocompromised Patients
title_sort evaluation of three commercial pcr assays for the detection of azole-resistant aspergillus fumigatus from respiratory samples of immunocompromised patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916969/
https://www.ncbi.nlm.nih.gov/pubmed/33670173
http://dx.doi.org/10.3390/jof7020132
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