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台湾地区临床分离株采用Sensititre YeastOne和VITEK2抗真菌药敏试验与CLSI肉汤微量稀释法的比较评估

Comparative evaluation of sensititre YeastOne and VITEK2 antifungal susceptibility tests with CLSI broth microdilution method of clinical isolates in Taiwan.

作者信息

Weng Tzu-Ping, Wang Shin-Wei, Lo Shih-Ting, Su Shu-Li, Hsieh Ming-I, Tsai Pei-Jane, Tsai Pei-Fang, Wu Chi-Jung, Lee Nan-Yao, Ko Wen-Chien, Chen Po-Lin

机构信息

Center for Infection Control, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

出版信息

Microbiol Spectr. 2025 Feb 4;13(2):e0211724. doi: 10.1128/spectrum.02117-24. Epub 2024 Dec 19.

Abstract

UNLABELLED

Commercial antifungal susceptibility tests were available for clinical yeast isolates. However, the updated Sensititre YeastOne (SYO) version YO10C excluded species for susceptibility testing. Uncorrelation of antifungal susceptibility patterns by SYO and therapeutic outcomes had been recently reported. We compared the performance of current commercial susceptibility tests with the standard CLSI broth microdilution (BMD) method for clinical isolates. Forty-seven clinical isolates were included from 1 January 2012 to 30 June 2023, among which 44 isolates were while 3 were . The performance of SYO version YO10C and VITEK2 YS09 was compared with the CLSI BMD method and correlated with MLST analysis and ERG11 mutation detection. Non-wild-type (non-WT) strains to amphotericin B (AMB) were observed in 11 isolates with the CLSI BMD method and 8 with SYO among 44 . isolates, but only 1 isolate was classified as non-WT by both methods. Additionally, all isolates were susceptible to AMB with their MIC ≤1 µg/mL according to the clinical breakpoint defined by EUCAST. Non-WT to FLC were observed in 5 . isolates with SYO, but they were classified as WT by CLSI BMD and VITEK2. The essential agreements between SYO and CLSI BMD were >90% to most antifungal agents except ITC in isolates (64%) and AMB in group (67%). Between SYO and CLSI BMD, the major error (ME) rates were 11% ( = 5) to FLC, 5% ( = 2) to ITC, and 2% ( = 1) to 5FC in isolates, and the very major error to 5FC was found in one isolate. ERG11 mutation with identical I199V was detected in 89% ( = 39) isolates, and 97% ( = 38) of them belonged to sequence type (ST) 5. The ERG11 mutation or cryptococcal ST was not associated with a decrease of antifungal susceptibilities. ME of FLC by SYO version YO10C compared to the CLSI BMD method reached up to 11% of isolates. The results of FLC MIC by SYO should be interpreted cautiously and correlated with therapeutic response, and further verification with the CLSI BMD method or VITEK2 is required.

IMPORTANCE

The study pointed out the major errors of fluconazole susceptibility results in clinical isolates between the commercial Sensititre YeastOne Susceptibility Plate version YO10C and the standard CLSI broth microdilution method. The results should be interpreted carefully with clinical correlation, and a different method of antifungal susceptibility testing should be considered if a discrepancy of susceptibility results is suspected.

摘要

未标注

临床酵母分离株可进行商业抗真菌药敏试验。然而,更新后的Sensititre YeastOne(SYO)版本YO10C排除了一些用于药敏试验的菌种。最近有报道称SYO的抗真菌药敏模式与治疗结果不相关。我们比较了当前商业药敏试验与标准CLSI肉汤微量稀释(BMD)法对临床分离株的性能。纳入了2012年1月1日至2023年6月30日期间的47株临床分离株,其中44株为[具体菌种1],3株为[具体菌种2]。将SYO版本YO10C和VITEK2 YS09的性能与CLSI BMD法进行比较,并与多位点序列分型(MLST)分析和ERG11突变检测相关联。在44株[具体菌种1]分离株中,用CLSI BMD法检测到11株对两性霉素B(AMB)为非野生型(non-WT)菌株,用SYO检测到8株,但两种方法均判定为非WT的仅1株。此外,根据欧盟CAST定义的临床折点,所有[具体菌种1]分离株对AMB均敏感,其MIC≤1μg/mL。用SYO检测到5株[具体菌种1]分离株对氟康唑(FLC)为非WT,但CLSI BMD法和VITEK2将它们判定为WT。SYO与CLSI BMD之间对大多数抗真菌药物的基本一致性在[具体菌种1]分离株中除伊曲康唑(ITC)为64%、[具体菌种2]组中AMB为67%外,均>90%。在SYO与CLSI BMD之间,[具体菌种1]分离株中对FLC的主要错误(ME)率为11%(n = 5),对ITC为5%(n = 2),对5-氟胞嘧啶(5FC)为2%(n = 1),在1株[具体菌种1]分离株中发现对5FC的极主要错误。在89%(n = 39)的[具体菌种1]分离株中检测到具有相同I199V的ERG11突变,其中97%(n = 38)属于序列型(ST)5。ERG11突变或隐球菌ST与抗真菌药敏性降低无关。与CLSI BMD法相比,SYO版本YO10C对FLC的ME在[具体菌种1]分离株中高达11%。SYO检测的FLC MIC结果应谨慎解读并与治疗反应相关联,需要用CLSI BMD法或VITEK2进行进一步验证。

重要性

该研究指出了商业Sensititre YeastOne药敏板版本YO10C与标准CLSI肉汤微量稀释法之间在临床[具体菌种1]分离株中氟康唑药敏结果的主要错误。结果应结合临床相关性仔细解读,如果怀疑药敏结果存在差异,应考虑采用不同的抗真菌药敏试验方法。

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