1. PCR-based detection of Aspergillus fumigatus and absence of azole resistance due to TR 34 /L98H in a french multicenter cohort of 137 patients with fungal rhinosinusitis.
- Author
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Morio F, Dannaoui E, Chouaki T, Cateau E, Malard O, Bonfils P, Page C, Dufour X, Cottrel C, Erwan T, Lavergne RA, and Le Pape P
- Subjects
- Adult, Aged, Aged, 80 and over, Antifungal Agents pharmacology, Aspergillosis epidemiology, Aspergillosis microbiology, Aspergillus fumigatus drug effects, Aspergillus fumigatus isolation & purification, Aspergillus fumigatus ultrastructure, Cohort Studies, Europe epidemiology, Female, Humans, Hyphae ultrastructure, Male, Microbial Sensitivity Tests, Middle Aged, Mutation, Missense, Polymerase Chain Reaction methods, Real-Time Polymerase Chain Reaction, Retrospective Studies, Young Adult, Aspergillosis diagnosis, Aspergillus fumigatus genetics, Azoles pharmacology, Drug Resistance, Fungal genetics, Rhinitis microbiology, Sinusitis microbiology
- Abstract
Fungal rhinosinusitis (FRS) has a worldwide distribution, comprises distinct clinical entities but is mostly due to Aspergillus among which Aspergillus fumigatus plays a major role in European countries. Although, there is accumulating evidence for the emergence of environmentally acquired-azole resistance in A. fumigatus (such as TR
34 /L98H) in various clinical settings, there is few data for patients with FRS. In this study, we aimed to investigate the prevalence of A. fumigatus azole resistance due to TR34 /L98H in a multicentre cohort of patients with FRS. One hundred and thirty-seven patients with FRS admitted between 2002 and 2016 at four French medical centres were retrospectively enrolled. Clinical and mycological findings were collected. Aspergillus fumigatus and the TR34 /L98H alteration conferring azole resistance were investigated directly from clinical samples using the commercial CE-IVD marked MycoGENIE® A. fumigatus real-time PCR assay. Fungal ball was the more frequent clinical form (n = 118). Despite the presence of fungal hyphae at direct microscopic examination, mycological cultures remained negative for 83 out of the 137 patients (60.6%). The PCR assay proved to be useful allowing the identification of A. fumigatus and etiological diagnosis in 106 patients (77.4%) compared with 44 patients (32.1%) when using culture as the reference method. Importantly, neither TR34 nor L98H alterations were evidenced., (© 2017 Blackwell Verlag GmbH.)- Published
- 2018
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