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硝呋太尔对尿路上分离出的抗真菌耐药菌的活性。

Activity of Nitroxoline in Antifungal-Resistant Species Isolated from the Urinary Tract.

机构信息

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

Department of Microbiology and Hospital Hygiene, Bundeswehr Central Hospital Koblenz, Koblenz, Germany.

出版信息

Antimicrob Agents Chemother. 2022 Jun 21;66(6):e0226521. doi: 10.1128/aac.02265-21. Epub 2022 May 11.

Abstract

Infections by drug-resistant fungi are increasingly reported worldwide; however, only few novel antifungals are being developed. The old antimicrobial nitroxoline is currently repurposed for oral treatment of bacterial urinary tract infections (UTI). Previously, antifungal activity has been demonstrated and in contrast to many antifungals nitroxoline reaches high urinary concentrations. In this study, the activity of nitroxoline was assessed in a collection of yeasts from the German National Reference Centre for Invasive Fungal Infections. Susceptibility was determined by broth microdilution (BMD) and disk diffusion (DD). The collection comprised 45 isolates originating from the urinary tract. MICs of amphotericin, anidulafungin and azoles were analyzed using EUCAST BMD. Among the collection isolates, resistance to antifungals was common, e.g., for fluconazole the MIC was 16/>64 mg/L; in contrast MIC of nitroxoline was 2/2 mg/L (MIC range 0.25-4 mg/L), which is at least two dilutions below the EUCAST breakpoint for uncomplicated UTI defined for E. coli (susceptible ≤ 16mg/L). Activity of nitroxoline was high irrespective of resistance to other agents. As BMD is labor-intensive, DD was investigated as an alternative method using three different agars. Nitroxoline disks produced large inhibition zones on all agars (≥19mm), but the correlation of MICs and zone diameters was low, with the highest correlation recorded for the CLSI recommended agar for antifungal DD (Pearson's r = -0,52). In conclusion, isolates of different species are highly susceptible to nitroxoline, which could be a promising antimicrobial to treat candiduria caused by multidrug resistant yeasts.

摘要

耐药真菌感染在全球范围内的报道越来越多;然而,目前正在开发的新型抗真菌药物却很少。目前,旧的抗菌药物硝呋太尔正被重新用于治疗细菌性尿路感染(UTI)的口服治疗。此前,已经证明了其具有抗真菌活性,与许多抗真菌药物不同的是,硝呋太尔可以达到很高的尿液浓度。在这项研究中,评估了来自德国侵袭性真菌感染国家参考中心的酵母的集合中的硝呋太尔的活性。通过肉汤微量稀释法(BMD)和药敏纸片扩散法(DD)测定了敏感性。该集合包括 45 株源自尿路感染的分离株。使用 EUCAST BMD 分析了两性霉素、阿尼达弗和唑类药物的 MIC。在分离株中,对各种抗真菌药物的耐药性很常见,例如氟康唑的 MIC 为 16/>64mg/L;相比之下,硝呋太尔的 MIC 为 2/2mg/L(MIC 范围为 0.25-4mg/L),至少比 EUCAST 定义的复杂性 UTI 的分界点低两个稀释度,复杂性 UTI 是指对大肠埃希菌的药敏试验(敏感 ≤ 16mg/L)。硝呋太尔的活性很高,与对其他药物的耐药性无关。由于 BMD 劳动强度大,因此研究了使用三种不同琼脂的 DD 作为替代方法。硝呋太尔药敏纸片在所有琼脂上产生了较大的抑菌圈(≥19mm),但 MIC 与抑菌圈直径之间的相关性较低,与 CLSI 推荐的用于抗真菌 DD 的琼脂的相关性最高(皮尔逊相关系数 r = -0.52)。总之,不同种属的分离株对硝呋太尔高度敏感,硝呋太尔可能是治疗多药耐药酵母引起的假丝酵母菌尿症的有前途的抗菌药物。

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