Use of Aspergillus fumigatus real-time PCR in bronchoalveolar lavage samples (BAL) for diagnosis of invasive aspergillosis, including azole-resistant cases, in high risk haematology patients: the need for a combined use with galactomannan.


Journal

Medical mycology
ISSN: 1460-2709
Titre abrégé: Med Mycol
Pays: England
ID NLM: 9815835

Informations de publication

Date de publication:
01 Nov 2019
Historique:
received: 10 10 2018
revised: 04 12 2018
accepted: 26 01 2019
pubmed: 13 2 2019
medline: 17 1 2020
entrez: 13 2 2019
Statut: ppublish

Résumé

Diagnosis of invasive aspergillosis (IA) is challenging, particularly in high-risk patients with lung lesions other than typical according to 2008-EORTC/MSG criteria. Even if microbiology is positive, they still remain unclassified according to 2008-EORTC/MSG. Quantitative polymerase chain reaction (qPCR) provides new mycological documentation of IA. This retrospective study assessed Aspergillus fumigatus real time qPCR (MycoGENIE®) in BAL to diagnose IA and identify azole-resistant strains. Clinical, radiological, and microbiological data from 114 hematology patients (69% HSCT recipients; 29% on mould active agents) from years 2012-2017 were collected; and 123 BAL samples were tested with qPCR (cutoff: Ct < 40) and galactomannan (GM, Platelia®, cutoff: 0.5 ODI). Patients were classified as proven/probable, possible, and no-IA. "Atypical-IA" referred to patients with lesions other than typical according to 2008-EORTC/MSG and positive mycology. Proven IA was diagnosed in two cases (1.6%), probable in 28 (22.8%), possible in 27 (22%), atypical in 14 (11.4%). qPCR was positive in 39 samples (31.7%). Sensitivity and specificity of qPCR for proven/probable IA (vs no-IA; atypical-IA excluded) were 40% (95% confidence interval [CI]: 23-59) and 69% (95%CI: 55-81), respectively. Sensitivity of qPCR was higher when combined with GM (83%, 95%CI: 65-94) and in those receiving mould-active agents at BAL (61%, 95%CI: 32-86). One sample had TR34/L98H mutation. In conclusion, in high-risk hematology patients with various lung lesions, A. fumigatus qPCR in BAL contributes to diagnosing IA, particularly if combined with GM and in patients receiving mould-active agents might allow detecting azole-resistant mutations in culture negative samples.

Identifiants

pubmed: 30753590
pii: 5309017
doi: 10.1093/mmy/myz002
pmc: PMC7107636
doi:

Substances chimiques

Mannans 0
galactomannan 11078-30-1
Galactose X2RN3Q8DNE

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

987-996

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology.

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Auteurs

Malgorzata Mikulska (M)

Division of Infectious Diseases, Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Elisa Furfaro (E)

Division of Infectious Diseases, Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.

Elena De Carolis (E)

Institute of Microbiology, Università Cattolica del Sacro Cuore - Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.

Enrico Drago (E)

School of Medicine, University of Genoa, Genoa, Italy.

Ilaria Pulzato (I)

Department of Radiology, University of Genoa, Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Maria Lucia Borghesi (ML)

Division of Infectious Diseases, Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Emanuela Zappulo (E)

Division of Infectious Diseases, Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.
Section of Infectious Diseases, Department of Clinical Medicine and Surgery, University of Naples "Federico II," Naples, Italy.

Anna Maria Raiola (AM)

Division of Hematology and Bone Marrow Transplantation, Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Carmen Di Grazia (CD)

Division of Hematology and Bone Marrow Transplantation, Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Valerio Del Bono (V)

Infectious Diseases Unit, Azienda Ospedaliera S. Croce e Carle, Cuneo, Italy.

Giuseppe Cittadini (G)

Department of Radiology, Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Emanuele Angelucci (E)

Division of Hematology and Bone Marrow Transplantation, Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

Maurizio Sanguinetti (M)

Institute of Microbiology, Università Cattolica del Sacro Cuore - Fondazione Policlinico Universitario Agostino Gemelli, Rome, Italy.

Claudio Viscoli (C)

Division of Infectious Diseases, Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Ospedale Policlinico San Martino-IRCCS per l'Oncologia, Genoa, Italy.

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