Multicentre determination of rezafungin (CD101) susceptibility of Candida species by the EUCAST method

被引:37
作者
Arendrup, M. C. [1 ,2 ,3 ]
Meletiadis, J. [4 ,5 ]
Zaragoza, O. [6 ]
Jorgensen, K. M. [1 ]
Marcos-Zambrano, L. J. [7 ]
Kanioura, L. [4 ]
Cuenca-Estrella, M. [6 ]
Mouton, J. W. [4 ]
Guinea, J. [7 ,8 ,9 ]
机构
[1] Statens Serum Inst, Unit Mycol, Bldg 43-317,Artillerivej 5, DK-2300 Copenhagen S, Denmark
[2] Rigshosp, Dept Clin Microbiol, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[4] Erasmus MC, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[5] Univ Athens, Attikon Univ Hosp, Clin Microbiol Lab, Athens, Greece
[6] Inst Salud Carlos III, Natl Ctr Microbiol, Mycol Reference Lab, Madrid, Spain
[7] Hosp Gen Univ Gregorio Maranon, Clin Microbiol & Infect Dis, Madrid, Spain
[8] Inst Invest Sanitaria Gregorio Maranon, Madrid, Spain
[9] CIBER Enfermedades Resp CIBERES CB06 06 0058, Madrid, Spain
关键词
Antifungal susceptibility; Candida; CD101; Echinocandin; EUCAST; IN-VITRO ACTIVITY; ECHINOCANDIN CD101; SPP; CLSI;
D O I
10.1016/j.cmi.2018.02.021
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Rezafungin (CD101) is a new long-acting echinocandin allowing weekly dosing, currently undergoing phase-II clinical trials for invasive candidiasis. The aim of this study was to assess rezafungin's in vitro activity against the most frequent Candida species following the EUCAST methodology. Methods: The susceptibility of 2018 clinical Candida isolates was determined at four European laboratories. In parallel, six control strains were repeatedly tested. Wild-type upper limits (WT-ULs), defined as the MIC value where the wild-type distribution ends, were determined following the principles for EUCAST ECOFF-setting. Results: The lowest rezafungin MICs (geometric MIC (GM-MIC), MIC range (mg/L)) were observed for C. albicans (0.016, 0.002-0.125) and the highest for C. parapsilosis (1.657, 0.063->4). MICs for the remaining species were in between these values (GM-MICs 0.048-0.055). Visual and statistical WT-ULs were identical for C. glabrata (0.125), C. krusei (0.125), C. parapsilosis (4), and C. tropicalis (0.25). If adopting these WT-ULs for classification into WT and non-WT populations, 1/413 C. glabrata, 1/402 C. krusei, 1/398 C. parapsilosis, and 1/402 C. tropicalis isolates were categorized as non-WT, all of which derived from Laboratory 1. For C. albicans unexplained laboratory variation was observed (WT-UL: 0.063-0.125 in Laboratories 1 and 2 versus 0.016 in Laboratories 3 and 4). A similar systematic difference was observed comparing the MICs for the three C albicans QC strains, specifically, obtained in Laboratories land 2 with those in Laboratories 3 and 4. Discussion: Rezafungin displayed species-specific activity similar to other echinocandins. Interlaboratory variation was observed for the most susceptible species C. albicans clinical and QC strains, an observation that warrants further investigation. (C) 2018 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1200 / 1204
页数:5
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