Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
J Antimicrob Chemother. 2019 May 1;74(5):1311-1316. doi: 10.1093/jac/dkz012.
The emergence of Neisseria gonorrhoeae resistant to all currently available antimicrobial therapies poses a dire public health threat. New antimicrobial agents with activity against N. gonorrhoeae are urgently needed. Apramycin is an aminocyclitol aminoglycoside with broad-spectrum in vitro activity against MDR Gram-negative pathogens and Staphylococcus aureus. However, its activity against N. gonorrhoeae has not been described.
The activity spectrum of apramycin against a collection of MDR N. gonorrhoeae was assessed. Isolates tested included those susceptible and resistant to the structurally distinct aminocyclitol, spectinomycin.
The modal MICs for apramycin and spectinomycin were 16 mg/L and 32 mg/L, respectively. The epidemiological cut-off (ECOFF) for apramycin was 64 mg/L. No strains among 77 tested had an MIC above this ECOFF, suggesting very low levels of acquired apramycin resistance. In time-kill analysis, apramycin demonstrated rapid bactericidal activity comparable to that of spectinomycin.
Apramycin has broad-spectrum, rapidly bactericidal activity against N. gonorrhoeae. Future pharmacokinetic and pharmacodynamic studies will be needed to determine whether apramycin and/or apramycin derivatives hold promise as new therapeutics for N. gonorrhoeae infection.
所有现有抗菌疗法都无法治疗的淋病奈瑟菌的出现,对公共卫生构成了严重威胁。迫切需要具有抗淋病奈瑟菌活性的新型抗菌药物。阿米卡星是一种氨基环醇氨基糖苷类药物,对耐多药革兰氏阴性病原体和金黄色葡萄球菌具有广泛的体外活性。然而,其对淋病奈瑟菌的活性尚未被描述。
评估了阿米卡星对一组耐多药淋病奈瑟菌的活性谱。测试的分离株包括对结构不同的氨基环醇大观霉素敏感和耐药的分离株。
阿米卡星和大观霉素的模式 MIC 分别为 16mg/L 和 32mg/L。阿米卡星的流行病学折点(ECOFF)为 64mg/L。在 77 株受试菌株中,没有一株的 MIC 高于该 ECOFF,这表明获得性阿米卡星耐药的水平非常低。在时间杀伤分析中,阿米卡星表现出与大观霉素相当的快速杀菌活性。
阿米卡星对淋病奈瑟菌具有广泛的杀菌活性。未来需要进行药代动力学和药效学研究,以确定阿米卡星和/或其衍生物是否有希望成为淋病奈瑟菌感染的新治疗药物。