Čipčić Paljetak Hana, Verbanac Donatella, Padovan Jasna, Dominis-Kramarić Miroslava, Kelnerić Željko, Perić Mihaela, Banjanac Mihailo, Ergović Gabrijela, Simon Nerrisa, Broskey John, Holmes David J, Eraković Haber Vesna
GlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia
GlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Antimicrob Agents Chemother. 2016 Aug 22;60(9):5337-48. doi: 10.1128/AAC.00524-16. Print 2016 Sep.
As we face an alarming increase in bacterial resistance to current antibacterial chemotherapeutics, expanding the available therapeutic arsenal in the fight against resistant bacterial pathogens causing respiratory tract infections is of high importance. The antibacterial potency of macrolones, a novel class of macrolide antibiotics, against key respiratory pathogens was evaluated in vitro and in vivo MIC values against Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus aureus, and Haemophilus influenzae strains sensitive to macrolide antibiotics and with defined macrolide resistance mechanisms were determined. The propensity of macrolones to induce the expression of inducible erm genes was tested by the triple-disk method and incubation in the presence of subinhibitory concentrations of compounds. In vivo efficacy was assessed in a murine model of S. pneumoniae-induced pneumonia, and pharmacokinetic (PK) profiles in mice were determined. The in vitro antibacterial profiles of macrolones were superior to those of marketed macrolide antibiotics, including the ketolide telithromycin, and the compounds did not induce the expression of inducible erm genes. They acted as typical protein synthesis inhibitors in an Escherichia coli transcription/translation assay. Macrolones were characterized by low to moderate systemic clearance, a large volume of distribution, a long half-life, and low oral bioavailability. They were highly efficacious in a murine model of pneumonia after intraperitoneal application even against an S. pneumoniae strain with constitutive resistance to macrolide-lincosamide-streptogramin B antibiotics. Macrolones are the class of macrolide antibiotics with an outstanding antibacterial profile and reasonable PK parameters resulting in good in vivo efficacy.
随着我们面临细菌对当前抗菌化疗药物的耐药性惊人增加,扩大对抗导致呼吸道感染的耐药细菌病原体的可用治疗武器库至关重要。在体外评估了一类新型大环内酯类抗生素——大环内酯酮对关键呼吸道病原体的抗菌效力,并测定了其对肺炎链球菌、化脓性链球菌、金黄色葡萄球菌和对大环内酯类抗生素敏感且具有明确大环内酯耐药机制的流感嗜血杆菌菌株的体内最低抑菌浓度(MIC)值。通过三碟法和在亚抑制浓度化合物存在下孵育来测试大环内酯酮诱导可诱导 erm 基因表达的倾向。在肺炎链球菌诱导的肺炎小鼠模型中评估体内疗效,并测定小鼠的药代动力学(PK)特征。大环内酯酮的体外抗菌谱优于市售的大环内酯类抗生素,包括酮内酯类泰利霉素,并且这些化合物不会诱导可诱导 erm 基因的表达。在大肠杆菌转录/翻译试验中,它们作为典型的蛋白质合成抑制剂起作用。大环内酯酮的特点是全身清除率低至中等、分布容积大、半衰期长且口服生物利用度低。即使对大环内酯 - 林可酰胺 - 链阳菌素 B 抗生素具有固有耐药性的肺炎链球菌菌株,腹腔注射后在肺炎小鼠模型中它们也具有高效性。大环内酯酮是一类具有出色抗菌谱和合理 PK 参数从而在体内具有良好疗效的大环内酯类抗生素。