Azole resistance in Aspergillus fumigatus isolates from respiratory specimens in Lyon University Hospitals, France: prevalence and mechanisms involved

泊沙康唑 烟曲霉 伊曲康唑 伏立康唑 微生物学 肉汤微量稀释 流出 生物 基因 抗药性 曲霉 基因表达 最小抑制浓度 遗传学 抗真菌 抗生素
作者
Loïc Simon,Tanguy Déméautis,Damien Dupont,Rolf Kramer,Héloïse Garnier,I. Durieu,A. Sénéchal,Philippe Reix,S. Couraud,Gilles Devouassoux,Bruno Lina,Méja Rabodonirina,Martine Wallon,Éric Dannaoui,Florence Persat,Jean Menotti
出处
期刊:International Journal of Antimicrobial Agents [Elsevier]
卷期号:58 (6): 106447-106447 被引量:7
标识
DOI:10.1016/j.ijantimicag.2021.106447
摘要

Resistance of Aspergillus fumigatus to triazoles has been reported increasingly in Europe. As few data are available from Southern France, the objectives of this study were to assess the burden of A. fumigatus isolates with azole resistance from clinical specimens in Lyon, and explore the resistance mechanisms involved. In this retrospective cross-sectional study, 221 consecutive A. fumigatus isolates from respiratory samples were identified from an 8-month period from 195 patients attending the Pulmonary Medicine Departments of Lyon University Hospitals. Morphological identification was confirmed by sequence analysis of the β-tubulin gene. All samples were tested for susceptibilities to itraconazole, voriconazole, posaconazole and isavuconazole using concentration gradient strips, and the results were confirmed using the EUCAST broth microdilution method. Resistance mechanisms were investigated by sequencing the cyp51A gene and its promoter, and by expression analysis of cyp51 and genes encoding several efflux transporters. Four isolates exhibited azole resistance. Three isolates presented with polymorphisms in an intronic region of cyp51A, and one isolate had F46Y, M172V and E427K polymorphisms. No mutations were identified in the cyp51A promoter, but significant induction of cyp51A and cyp51B gene expression was observed for all four and three isolates, respectively. Significant induction of atrF and cdr1B gene expression was observed for two and three isolates, respectively. No significant induction of MDR1/2/3/4, MFS56 and M85 gene expression was observed. To conclude, the observed prevalence of azole resistance was 2.1%. Significant induction of expression of the cyp51 genes and two genes encoding efflux transporters was evidenced, underlying the diversity of resistance mechanisms to be explored.
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