Laboratoire de Chimie de Coordination du CNRS, 205 Route de Narbonne, BP 44099, 31077 Toulouse Cedex 4, France.
LCC-CNRS, Université de Toulouse, CNRS, 31400 Toulouse, France.
Biomacromolecules. 2023 Jul 10;24(7):3215-3227. doi: 10.1021/acs.biomac.3c00266. Epub 2023 Jun 3.
The incessant, global increase in antimicrobial resistance (AMR) is a very big challenge for healthcare systems. AMR is predicted to grow at an alarming pace, with a dramatic increase in morbidity, mortality, and a 100 trillion US$ loss to the global economy by 2050. The mortality rate caused by methicillin-resistant . (MRSA) is much higher as compared to infections caused by drug-susceptible . . Additionally, there is a big paucity of therapeutics available for treatment of serious infections caused by MRSA. Thus, the discovery and development of novel therapies is an urgent, unmet medical need. In this context, we synthesized AE4G0, a low-generation cationic-phosphorus dendrimer expressing potent antimicrobial activity against . and sp., and demonstrating a broad selectivity index against eukaryotic cells. AE4G0 exhibits concentration-dependent, bactericidal activity and synergizes with gentamicin, especially against gentamicin-resistant MRSA NRS119. Fluorescence and scanning electron microscopy demonstrate that treatment with AE4G0 led to the utter destruction of . ATCC 29213 without inducing resistance, despite repeated exposure. When tested , AE4G0 demonstrates significant efficacy against . ATCC 29213, alone and in combination with gentamicin against gentamicin-resistant . NRS119 in the murine skin model of infection. Taken together, AE4G0 demonstrates the potential to be translated as a novel therapeutic option for the treatment of topical, drug-resistant . infections.
不断增加的全球抗菌药物耐药性(AMR)是对医疗保健系统的一个巨大挑战。预计 AMR 将以惊人的速度增长,发病率、死亡率将大幅上升,到 2050 年,全球经济将损失 100 万亿美元。耐甲氧西林金黄色葡萄球菌(MRSA)引起的死亡率要远远高于对药物敏感的金黄色葡萄球菌引起的感染。此外,用于治疗由 MRSA 引起的严重感染的治疗方法非常有限。因此,发现和开发新的治疗方法是一个迫切的、未满足的医疗需求。在这种情况下,我们合成了 AE4G0,一种低代阳离子磷树突状聚合物,对金黄色葡萄球菌和表皮葡萄球菌具有强大的抗菌活性,并对真核细胞具有广泛的选择性指数。AE4G0 表现出浓度依赖性的杀菌活性,并与庆大霉素协同作用,特别是对庆大霉素耐药的 MRSA NRS119。荧光和扫描电子显微镜表明,尽管反复暴露,AE4G0 治疗可导致金黄色葡萄球菌 ATCC 29213 完全破坏,而不会诱导耐药性。当用于测试时,AE4G0 单独使用或与庆大霉素联合使用,对感染的小鼠皮肤模型中的 ATCC 29213 具有显著疗效。综上所述,AE4G0 具有转化为治疗局部、耐药金黄色葡萄球菌感染的新型治疗选择的潜力。