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马来西亚临床分离株的体外抗真菌药敏谱

In vitro Antifungal Susceptibility Profile of Clinical in Malaysia.

作者信息

Tan Xue Ting, Mokhtar Nurin Nazirah, Hassan Murnihayati, Tang Min Moon

机构信息

Bacteriology Unit, Infectious Diseases Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Setia Alam, Selangor, Malaysia.

Department of Dermatology, Hospital Umum Sarawak, Ministry of Health Malaysia, Kuching, Sarawak, Malaysia.

出版信息

Infect Drug Resist. 2025 May 5;18:2291-2299. doi: 10.2147/IDR.S513536. eCollection 2025.

Abstract

PURPOSE

This study aimed to determine the antifungal susceptibility pattern of clinical isolates in Malaysia.

PATIENTS AND METHODS

Eight clinical strains of the were received from various Malaysian hospitals from the year 2020 until 2024. The isolates were obtained from patients with clinical presentations suggestive of cutaneous fungal infection. Their identities were determined using microscopic, macroscopic and molecular methods, specifically internal transcribed spacer (ITS) sequencing. Next, the antifungal susceptibility of amphotericin B, itraconazole, fluconazole, voriconazole, ravuconazole, posaconazole, ketoconazole, isavuconazole, flucytosine and terbinafine against the were determined using broth microdilution method as outlined in the Clinical and Laboratory Standards Institute (CLSI) M38 guideline. The geometric means (GM) of minimum inhibitory concentration (MIC), MIC, and MIC were determined for each antifungal. Subsequently, the Kruskal-Wallis test was performed to determine the significant difference observed in the median MIC values between the different antifungal groups (azole, polyene, pyrimidine and allylamine) against the isolate. The significance value was set at <0.05.

RESULTS

The GM MIC, MIC and MIC of all tested antifungals except amphotericin B and fluconazole against the were ≤0.25 μg/mL. In contrast, amphotericin B and fluconazole exhibited higher MICs ranging from 2 to 16 μg/mL. Furthermore, the Kruskal-Wallis test revealed a significant difference in the median MIC values across all antifungals, with a -value of 4.94 × 10⁻.

CONCLUSION

In conclusion, all the isolates in this study were susceptible to pyrimidine, allylamine, and azoles, while showing intermediate susceptibility to fluconazole and notable resistance to amphotericin B. Additionally, itraconazole and terbinafine could be recommended as the first-line therapy option, which was supported by their demonstrated efficacy (MIC ≤0.03 μg/mL) and clinical improvement observed in this study.

摘要

目的

本研究旨在确定马来西亚临床分离株的抗真菌药敏模式。

患者与方法

2020年至2024年期间,从马来西亚各医院收到了8株[未提及具体真菌名称]临床菌株。这些分离株取自临床表现提示皮肤真菌感染的患者。通过显微镜、宏观和分子方法,特别是内部转录间隔区(ITS)测序来确定它们的身份。接下来,按照临床和实验室标准协会(CLSI)M38指南中概述的肉汤微量稀释法,测定两性霉素B、伊曲康唑、氟康唑、伏立康唑、雷夫康唑、泊沙康唑、酮康唑、艾沙康唑、氟胞嘧啶和特比萘芬对[未提及具体真菌名称]的抗真菌药敏性。测定每种抗真菌药物的最低抑菌浓度(MIC)、MIC₅₀和MIC₉₀的几何平均值(GM)。随后,进行Kruskal-Wallis检验,以确定不同抗真菌药物组(唑类、多烯类、嘧啶类和烯丙胺类)对分离株的MIC中位数之间观察到的显著差异。显著性值设定为<0.05。

结果

除两性霉素B和氟康唑外,所有测试抗真菌药物对[未提及具体真菌名称]的GM MIC、MIC₅₀和MIC₉₀均≤0.25μg/mL。相比之下,两性霉素B和氟康唑的MIC较高,范围为2至16μg/mL。此外,Kruskal-Wallis检验显示所有抗真菌药物的MIC中位数存在显著差异,P值为4.94×10⁻[此处P值未完整给出]。

结论

总之,本研究中的所有[未提及具体真菌名称]分离株对嘧啶类、烯丙胺类和唑类敏感,而对氟康唑表现出中度敏感性,对两性霉素B表现出显著耐药性。此外,伊曲康唑和特比萘芬可被推荐作为一线治疗选择,本研究中观察到的疗效(MIC≤0.03μg/mL)和临床改善支持了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/689f/12063617/f84eba1f1cbc/IDR-18-2291-g0001.jpg

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