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硝呋太尔对耳念珠菌分离株的抗真菌活性。

Antifungal activity of nitroxoline against Candida auris isolates.

机构信息

Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Medical Faculty and University Hospital of Cologne, Cologne, Germany.

MVZ Labor Limbach und Kollegen, Heidelberg, Germany.

出版信息

Clin Microbiol Infect. 2021 Nov;27(11):1697.e7-1697.e10. doi: 10.1016/j.cmi.2021.06.035. Epub 2021 Jul 7.

Abstract

OBJECTIVES

To investigate the in vitro activity of nitroxoline against a molecularly characterized collection of clinical Candida auris isolates.

METHODS

Thirty-five clinical isolates of C. auris from diverse sources representing all five different C. auris clades were included in the study. Nitroxoline activity was assessed using broth microdilution. Additionally, susceptibility testing by disc diffusion was assessed on RPMI-1640 and Müller-Hinton agar plates. Minimal inhibitory concentrations of the antifungals fluconazole, voriconazole, amphotericin B and anidulafungin were determined.

RESULTS

Nitroxoline MICs ranged from 0.125 to 1 mg/L (MIC 0.25/0.5 mg/L). Compared with amphotericin B (MIC >1 mg/L in 4/35 isolates), anidulafungin (MIC >0.06 mg/L in 26/35 isolates) and fluconazole (MIC >4 mg/L in 31/35 isolates), in vitro activity of nitroxoline was high. Isolates belonging to clade I had marginally lower nitroxoline MICs (range 0.125-0.5 mg/L, mean MIC 0.375 mg/L) compared with clade III (range 0.5-1 mg/L, mean MIC 0.7 mg/L; p = 0.0094). The correlation of MIC and inhibition zones by disc diffusion was good when using RPMI-agar for disc diffusion, with a Pearson's correlation coefficient of -0.74 (95% CI -0.86 to -0.54).

CONCLUSIONS

Nitroxoline has excellent in vitro activity against C. auris isolates, with MICs of 0.125-1 mg/L (for comparison, the EUCAST breakpoint for uncomplicated urinary tract infection with Escherichia coli is ≤ 16 mg/L). It is an approved, well-tolerated antimicrobial that achieves high urinary concentrations after oral administration and could be a useful treatment option in C. auris candiduria.

摘要

目的

研究硝呋太尔对经过分子特征鉴定的临床分离的耳念珠菌菌株的体外活性。

方法

本研究纳入了来自不同来源的 35 株耳念珠菌临床分离株,代表了耳念珠菌的五个不同进化枝。使用肉汤微量稀释法评估硝呋太尔的活性。此外,还在 RPMI-1640 和 Mueller-Hinton 琼脂平板上评估了药敏纸片扩散法的药敏性。测定了抗真菌药物氟康唑、伏立康唑、两性霉素 B 和安尼芬净的最小抑菌浓度。

结果

硝呋太尔的 MIC 范围为 0.125 至 1 mg/L(MIC 0.25/0.5 mg/L)。与两性霉素 B(4/35 株的 MIC >1 mg/L)、安尼芬净(26/35 株的 MIC >0.06 mg/L)和氟康唑(35 株的 MIC >4 mg/L)相比,硝呋太尔的体外活性较高。属于进化枝 I 的分离株的硝呋太尔 MIC 略低(范围 0.125-0.5 mg/L,平均 MIC 0.375 mg/L),而属于进化枝 III 的分离株的硝呋太尔 MIC 较高(范围 0.5-1 mg/L,平均 MIC 0.7 mg/L;p = 0.0094)。使用 RPMI 琼脂进行药敏纸片扩散时,MIC 与抑菌圈直径的相关性较好,Pearson 相关系数为-0.74(95% CI -0.86 至 -0.54)。

结论

硝呋太尔对耳念珠菌分离株具有极好的体外活性,MIC 值为 0.125-1 mg/L(相比之下,欧盟药敏试验委员会(EUCAST)对大肠埃希菌引起的单纯性尿路感染的折点为≤16 mg/L)。它是一种已批准使用的、耐受性良好的抗菌药物,口服后可在尿液中达到高浓度,可能是治疗耳念珠菌菌尿症的一种有用的治疗选择。

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