Comparison of MIC Test Strip and reference broth microdilution method for amphotericin B and azoles susceptibility testing on wild type and non-wild type Aspergillus species.

IF 2.7 3区 医学 Q3 INFECTIOUS DISEASES Medical mycology Pub Date : 2025-01-27 DOI:10.1093/mmy/myaf006
Katherine Hermida-Alava, Santiago Pola, Guillermo García-Effrón, María L Cuestas
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Abstract

This study was performed to evaluate whether the MIC Test Strip (MTS) quantitative assay for determining the minimum inhibitory concentration (MIC) correlated with the CLSI reference broth microdilution method (BMD) for antifungal susceptibility testing of wild-type and non-wild-type Aspergillus species isolated from cystic fibrosis patients against antifungal agents known to be usually effective against Aspergillus spp. This study was performed to assist in the decision-making process for possible deployment of the MTS assay for antimicrobial susceptibility testing of Aspergillus species into regional public health laboratories of Mycology due to difficulties in equipping the reference BMD methods in a laboratory routine. For this purpose, a set of 40 phenotypically diverse isolates (27 wild-type, 9 non-wild-type, and 4 species with reduced susceptibility to azoles and amphotericin B (AMB)) collected from clinical samples were tested. MICs were performed by both MTS and reference BMD for AMB, and azoles. MTS results for posaconazole correlated well with reference BMD rendering an almost perfect agreement (kappa value = 1.000) by category interpretation (CI)/category distribution of MICs (CDM) (100%) while voriconazole MTS results yielded a substantial correlation with BMD (kappa value = 0.788) by CI/CDM (97.5%). In contrast, itraconazole and AMB yielded the poorest correlation with BMD, rendering a moderate agreement (kappa values of 0.554 and 0.437, respectively) by CI/CDM (87.5% and 85%, respectively). In conclusion, the MTS method represents a valid option for antimicrobial susceptibility testing of Aspergillus species against posaconazole and voriconazole. Itraconazole and AMB MTS results showed some concerning lack of correlation with the corresponding reference BMD results.

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在对野生型和非野生型曲霉菌种进行两性霉素 B 和唑类药物药敏试验时,比较 MIC 测试条和参考肉汤微量稀释法。
本研究旨在评估用于确定最低抑菌浓度(MIC)的 MIC 检测条(MTS)定量检测法与 CLSI 参考肉汤微量稀释法(BMD)是否相关,后者用于检测从囊性纤维化患者中分离出的野生型和非野生型曲霉菌对已知通常对曲霉菌属有效的抗真菌药物的抗真菌药敏性。这项研究的目的是协助决策过程,以便在地区性公共卫生真菌学实验室中采用 MTS 检测法进行曲霉菌抗菌药敏感性检测,因为在实验室常规工作中很难配备 BMD 参考方法。为此,我们对从临床样本中采集的 40 个表型不同的分离株(27 个野生型、9 个非野生型和 4 个对唑类和两性霉素 B(AMB)敏感性降低的菌种)进行了测试。通过 MTS 和参考 BMD 对 AMB 和唑类进行了 MIC 测定。泊沙康唑的 MTS 结果与参考 BMD 有很好的相关性,通过类别解释 (CI)/ MICs 的类别分布 (CDM) 几乎完全一致(卡帕值 = 1.000)(100%),而伏立康唑的 MTS 结果与 BMD 有很大的相关性(卡帕值 = 0.788),通过 CI/CDM 几乎完全一致(97.5%)。相比之下,伊曲康唑和 AMB 与 BMD 的相关性最差,CI/CDM(分别为 87.5%和 85%)显示两者的相关性为中等(kappa 值分别为 0.554 和 0.437)。总之,MTS 法是曲霉菌对泊沙康唑和伏立康唑进行抗菌药敏感性检测的有效方法。伊曲康唑和 AMB MTS 结果与相应的参考 BMD 结果缺乏相关性。
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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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