Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Medical Faculty and University Hospital of Cologne, Cologne, Germany.
DZIF (German Centre for Infection Research), partner site Bonn-Cologne, Cologne, Germany.
J Antimicrob Chemother. 2019 Oct 1;74(10):2934-2937. doi: 10.1093/jac/dkz275.
Infections caused by carbapenemase-producing Enterobacterales (CPE) constitute a major global health concern and are associated with increased morbidity and mortality. Nitroxoline is an old antibiotic, which has recently been re-launched for the treatment of uncomplicated urinary tract infection. Because of low resistance rates it could be an interesting option for treatment of MDR isolates, yet data on CPE susceptibility are scarce.
To analyse the in vitro activity of nitroxoline against CPE.
MICs of nitroxoline were determined by agar dilution for a collection of well-characterized carbapenemase producers (n = 105), producing OXA-48-like (n = 36), VIM (n = 21), IMI (n = 9), IMP (n = 6), NDM (n = 22), KPC (n = 11), OXA-58 (n = 2) and GES (n = 2). For comparison, MICs of ertapenem, imipenem and meropenem were determined by agar gradient diffusion.
For all 105 isolates, the MIC50/90 of nitroxoline was 8/16 mg/L. All Escherichia coli isolates (30/30, 100%) showed low MICs of 2-8 mg/L and were susceptible to nitroxoline. MICs of 32 mg/L were recorded for five isolates of VIM- and IMI-producing Enterobacter cloacae (n = 3) and OXA- and VIM-producing Klebsiella pneumoniae (n = 2).
Nitroxoline exhibited excellent in vitro activity against most isolates producing common and rare carbapenemases. If the current EUCAST susceptibility breakpoint of ≤16 mg/L for E. coli in uncomplicated urinary tract infections was applied, 95.2% (100/105) of isolates would be classified as susceptible. Nitroxoline could therefore be an alternative oral option for treatment of uncomplicated urinary tract infections caused by CPE.
产碳青霉烯酶肠杆菌科(CPE)引起的感染是一个主要的全球健康问题,与发病率和死亡率的增加有关。硝呋太尔是一种新型抗生素,最近被重新用于治疗单纯性尿路感染。由于耐药率低,它可能是治疗多药耐药株的一个有趣选择,但关于 CPE 药敏的数据却很少。
分析硝呋太尔对 CPE 的体外活性。
通过琼脂稀释法测定了一组特征明确的碳青霉烯酶生产者(n=105)的硝呋太尔 MIC,其中包括产 OXA-48 样(n=36)、VIM(n=21)、IMI(n=9)、IMP(n=6)、NDM(n=22)、KPC(n=11)、OXA-58(n=2)和 GES(n=2)。为了比较,通过琼脂梯度扩散法测定了厄他培南、亚胺培南和美罗培南的 MIC。
对于所有 105 株分离株,硝呋太尔的 MIC50/90 为 8/16mg/L。所有大肠埃希菌分离株(30/30,100%)均显示出 2-8mg/L 的低 MIC 值,对硝呋太尔敏感。产 VIM 和 IMI 的阴沟肠杆菌(n=3)和产 OXA 和 VIM 的肺炎克雷伯菌(n=2)的 5 株分离株的 MIC 值为 32mg/L。
硝呋太尔对大多数产常见和罕见碳青霉烯酶的分离株表现出极好的体外活性。如果目前欧盟药敏标准中对单纯性尿路感染中大肠埃希菌的敏感性分界点为≤16mg/L,则 105 株分离株中有 95.2%(100/105)被归类为敏感。因此,硝呋太尔可能是治疗 CPE 引起的单纯性尿路感染的一种替代口服选择。