Emergence of azole-resistant invasive aspergillosis in HSCT recipients in Germany

被引:153
作者
Steinmann, J. [1 ]
Hamprecht, A. [2 ]
Vehreschild, M. J. G. T. [3 ,4 ]
Cornely, O. A. [3 ,5 ]
Buchheidt, D. [6 ]
Spiess, B. [6 ]
Koldehoff, M. [7 ]
Buer, J. [1 ]
Meis, J. F. [8 ,9 ]
Rath, P-M. [1 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Inst Med Microbiol, Essen, Germany
[2] Univ Hosp Cologne, Inst Med Microbiol Immunol & Hyg, Cologne, Germany
[3] Univ Cologne, Dept Internal Med 1, D-50931 Cologne, Germany
[4] German Ctr Infect Res DZIF, Bonn, Germany
[5] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, Ctr Integrated Oncol CIO Koln Bonn, Clin Trials Ctr Cologne,ZKS Koln,BMBF 01KN1106, D-50931 Cologne, Germany
[6] Heidelberg Univ, Mannheim Univ Hosp, Dept Internal Med 3, Mannheim, Germany
[7] Univ Hosp Essen, West German Canc Ctr, Dept Bone Marrow Transplantat AHE, Essen, Germany
[8] Canisius Wilhelmina Hosp, Dept Med Microbiol & Infect Dis, Nijmegen, Netherlands
[9] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, NL-6525 ED Nijmegen, Netherlands
关键词
azole resistance; Aspergillus fumigatus; haematopoietic stem cell transplant recipients; FUMIGATUS; TR46/Y121F/T289A; MUTATION; INDIA;
D O I
10.1093/jac/dku566
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Aspergillus fumigatus is the most common agent of invasive aspergillosis (IA). In recent years, resistance to triazoles, the mainstay of IA therapy, has emerged in different countries worldwide. IA caused by azole-resistant A. fumigatus (ARAF) shows an exceedingly high mortality. In this study, IA due to ARAF isolates in HSCT recipients in Germany was investigated. Methods: The epidemiology of azole resistance in IA was analysed in two German haematology departments. Between 2012 and 2013, 762 patients received HSCT in Essen (n = 388) and Cologne (n = 374). Susceptibility testing of A. fumigatus isolates was performed by Etest, followed by EUCAST broth microdilution testing if elevated MICs were recorded. In all ARAF isolates the cyp51A gene was sequenced and the genotype was determined by microsatellite typing using nine short tandem repeats. Results: In total, A. fumigatus was recovered from 27 HSCT recipients. Eight patients had azole-resistant IA after HSCT, and seven of the cases were fatal (88%). All except one patient received antifungal prophylaxis (in five cases triazoles). TR34/L98H was the most common mutation (n = 5), followed by TR46/Y121F/T289A (n = 2). In one resistant isolate no cyp51A mutation was detected. Genotyping revealed genetic diversity within the German ARAF isolates and no clustering with resistant isolates from the Netherlands, India and France. Conclusions: This report highlights the emergence of azole-resistant IA with TR34/L98H and TR46/Y121F/T289A mutations in HSCT patients in Germany and underscores the need for systematic antifungal susceptibility testing of A. fumigatus.
引用
收藏
页码:1522 / 1526
页数:5
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