Farrell D J, Sader H S, Rhomberg P R, Scangarella-Oman N E, Flamm R K
JMI Laboratories, North Liberty, Iowa, USA.
GlaxoSmithKline, Collegeville, Pennsylvania, USA.
Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.02047-16. Print 2017 Mar.
Gepotidacin (formerly GSK2140944) is a novel, first-in-class, triazaacenaphthylene antibacterial that inhibits bacterial DNA gyrase and topoisomerase IV via a unique mechanism and has demonstrated activity against , including drug-resistant strains, and also targets pathogens associated with other conventional and biothreat infections. Broth microdilution was used to evaluate the MIC and minimum bactericidal concentration (MBC) activity of gepotidacin and comparators against 25 strains (including five ciprofloxacin-nonsusceptible strains). Gepotidacin activity was also evaluated against three strains (including a ciprofloxacin-nonsusceptible strain) for resistance development, against three strains (including two tetracycline- and azithromycin-nonsusceptible strains) using time-kill kinetics and checkerboard methods, and against two strains for the investigation of postantibiotic (PAE) and subinhibitory (PAE-SME) effects. The MIC and MIC for gepotidacin against the 25 isolates tested were 0.12 and 0.25 μg/ml, respectively. The MBC and MBC for gepotidacin were 0.25 and 0.5 μg/ml, respectively. Gepotidacin was bactericidal, and single-step resistance selection studies did not recover any mutants, indicating a low rate of spontaneous single-step resistance. For combinations of gepotidacin and comparators tested using checkerboard methods, there were no instances where antagonism occurred and only one instance of synergy (with moxifloxacin; fractional inhibitory concentration, 0.375). This was not confirmed by time-kill studies. The PAE for gepotidacin against the wild-type strain ranged from 0.5 to >2.5 h, and the PAE-SME was >2.5 h. These data indicate that further study of gepotidacin is warranted for potential use in treating infections caused by .
吉波沙星(曾用名GSK2140944)是一种新型的、同类首创的三氮杂蒽二酮类抗菌药物,它通过独特机制抑制细菌DNA回旋酶和拓扑异构酶IV,已显示出对包括耐药菌株在内的[具体细菌名称未给出]具有活性,并且还针对与其他传统感染和生物威胁感染相关的病原体。采用肉汤微量稀释法评估吉波沙星及对照药物对25株[具体细菌名称未给出](包括5株对环丙沙星不敏感的菌株)的最低抑菌浓度(MIC)和最低杀菌浓度(MBC)活性。还针对3株[具体细菌名称未给出](包括1株对环丙沙星不敏感的菌株)评估了吉波沙星的耐药性发展情况,针对3株[具体细菌名称未给出](包括2株对四环素和阿奇霉素不敏感的菌株)采用时间杀菌动力学和棋盘法进行评估,并针对2株[具体细菌名称未给出]研究抗生素后效应(PAE)和亚抑菌效应(PAE - SME)。吉波沙星对所测试的25株[具体细菌名称未给出]分离株的MIC和MIC50分别为0.12和0.25μg/ml。吉波沙星的MBC和MBC50分别为0.25和0.5μg/ml。吉波沙星具有杀菌作用,单步耐药性选择研究未发现任何突变体,表明自发单步耐药率较低。对于使用棋盘法测试的吉波沙星与对照药物的组合,未出现拮抗情况,仅出现1例协同作用(与莫西沙星;部分抑菌浓度为0.375)。时间杀菌研究未证实这一点。吉波沙星对野生型菌株 的PAE范围为0.5至>2.5小时,PAE - SME大于2.5小时。这些数据表明,有必要对吉波沙星进行进一步研究,以探讨其在治疗由[具体细菌名称未给出]引起的感染中的潜在用途。