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一种抗分枝杆菌的共轭寡聚电解质,对有效。

An anti-mycobacterial conjugated oligoelectrolyte effective against .

机构信息

Department of Chemistry, National University of Singapore, 4 Science Drive 2, 117543 Singapore, Singapore.

Center for Polymers and Organic Solids, Department of Chemistry and Biochemistry, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.

出版信息

Sci Transl Med. 2024 Feb 21;16(735):eadi7558. doi: 10.1126/scitranslmed.adi7558.

Abstract

Infections caused by nontuberculous mycobacteria have increased more than 50% in the past two decades and more than doubled in the elderly population. (Mab), one of the most prevalent of these rapidly growing species, is intrinsically resistant to numerous antibiotics. Current standard-of-care treatments are not satisfactory, with high failure rate and notable adverse effects. We report here a potent anti-Mab compound from the flexible molecular framework afforded by conjugated oligoelectrolytes (COEs). A screen of structurally diverse, noncytotoxic COEs identified a lead compound, COE-PNH, which was bactericidal against replicating, nonreplicating persisters and intracellular Mab.COE-PNH had low propensity for resistance development, with a frequency of resistance below 1.25 × 10 and showed no detectable resistance upon serial passaging. Mechanism of action studies were in line with COE-PNH affecting the physical and functional integrity of the bacterial envelope and disrupting the mycomembrane and associated essential bioenergetic pathways. Moreover, COE-PNH was well-tolerated and efficacious in a mouse model of Mab lung infection. This study highlights desirable in vitro and in vivo potency and safety index of this COE structure, which represents a promising anti-mycobacterial to tackle an unmet medical need.

摘要

在过去的二十年中,非结核分枝杆菌引起的感染增加了 50%以上,在老年人群中增加了一倍以上。(Mab)是这些快速生长的物种中最常见的一种,对许多抗生素具有内在抗性。目前的标准治疗方法并不令人满意,失败率高,不良反应明显。我们在这里报告一种来自共轭低聚物(COE)提供的灵活分子框架的有效抗 Mab 化合物。对结构多样、非细胞毒性的 COE 进行筛选,确定了一种先导化合物 COE-PNH,该化合物对复制、非复制的持续存在者和细胞内 Mab 具有杀菌作用。COE-PNH 不易产生耐药性,耐药频率低于 1.25×10,连续传代后无耐药性。作用机制研究表明,COE-PNH 影响细菌包膜的物理和功能完整性,并破坏真菌膜和相关必需的生物能量途径。此外,COE-PNH 在 Mab 肺部感染的小鼠模型中具有良好的耐受性和疗效。这项研究突出了这种 COE 结构在体外和体内的高活性和安全性指数,代表了一种有前途的抗分枝杆菌药物,可以解决未满足的医疗需求。

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