Postgraduate Program in Bioscience & Physiopathology, State University of Maringa, Maringa, Parana, Brazil.
Postgraduate Program in Health Sciences, State University of Maringa, Parana, Brazil.
Future Microbiol. 2024;19(17):1445-1454. doi: 10.1080/17460913.2024.2398312. Epub 2024 Sep 11.
Polymyxin B (PMB) is one of the few therapeutic options for treating infections caused by carbapenem-resistant Gram-negative bacteria (CR-GNB). However, the emergence of PMB-resistant CR-GNB strains has prompted the exploration of antibiotic adjuvants as potential therapeutic avenues. Thus, this study evaluates the potential of 3,5-dinitrobenzoic acid derivatives (DNH01, DNH11, DNH13 and DNH20) and isoniazid--acylhydrazones (INZ1-7, INZ9 and INZ11) as adjuvants to enhance PMB efficacy against CR-GNB. MIC, MBC and drug combination assays were conducted using multidrug-resistant clinical isolates of and . In addition, the effects of PMB and PMB + DNH derivatives were assessed through flow cytometry and scanning electron microscopy (SEM). DNH01, DNH11 and DNH20, unlike the INH-acylhydrazones, significantly restored PMB activity (MIC ≤ 2 μg/ml) in 80% of the tested isolates. Flow cytometry and SEM assays confirmed that DNH derivatives rescued the activity of PMB, yielding results comparable to those expected for PMB alone but at 256-fold lower concentrations. These findings suggest DNH derivatives hold substantial promise as PMB adjuvants to combat PMB-resistant CR-GNB infections.
多黏菌素 B(PMB)是治疗碳青霉烯类耐药革兰氏阴性菌(CR-GNB)感染的少数治疗选择之一。然而,PMB 耐药 CR-GNB 菌株的出现促使人们探索抗生素佐剂作为潜在的治疗途径。因此,本研究评估了 3,5-二硝基苯甲酸衍生物(DNH01、DNH11、DNH13 和 DNH20)和异烟肼-酰肼(INZ1-7、INZ9 和 INZ11)作为佐剂增强 PMB 对 CR-GNB 疗效的潜力。使用多药耐药临床分离株和 进行 MIC、MBC 和药物组合测定。此外,通过流式细胞术和扫描电子显微镜(SEM)评估 PMB 和 PMB+DNH 衍生物的作用。与 INH-酰肼不同,DNH01、DNH11 和 DNH20 显著恢复了 80%测试分离株中 PMB 的活性(MIC≤2μg/ml)。流式细胞术和 SEM 测定证实,DNH 衍生物挽救了 PMB 的活性,产生的结果与单独使用 PMB 相当,但浓度低 256 倍。这些发现表明 DNH 衍生物作为 PMB 佐剂具有很大的潜力,可以对抗 PMB 耐药的 CR-GNB 感染。