Suppr超能文献

小分子 IITR00693(2-氨基三亚甲基蜜胺)增强多黏菌素 B 对 和 的活性。

Small Molecule IITR00693 (2-Aminoperimidine) Synergizes Polymyxin B Activity against and .

机构信息

Department of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Uttarakhand247 667, India.

Department of Microbiology, All India Institute of Medical Sciences, Rishikesh, Uttarakhand249 201, India.

出版信息

ACS Infect Dis. 2023 Mar 10;9(3):692-705. doi: 10.1021/acsinfecdis.2c00622. Epub 2023 Jan 30.

Abstract

The rise of antibiotic resistance among skin-infecting pathogens poses an urgent threat to public health and has fueled the search for new therapies. Enhancing the potency of currently used antibiotics is an alternative for the treatment of infections caused by drug-resistant pathogens. In this study, we aimed to identify a small molecule that can potentiate currently used antibiotics. IITR00693 (2-aminoperimidine), a novel antibacterial small molecule, potentiates the antibacterial activity of polymyxin B against and . Herein, we investigated in detail the mode of action of this interaction and the molecule's capability to combat soft-tissue infections caused by and . A microdilution checkerboard assay was performed to determine the synergistic interaction between polymyxin B and IITR00693 in clinical isolates of and . Time-kill kinetics, post-antibiotic effect, and resistance generation studies were performed to assess the pharmacodynamics of the combination. Assays based on different fluorescent probes were performed to decipher the mechanism of action of this combination. The efficacy of the IITR00693-polymyxin B combination was determined in a murine acute wound infection model. IITR00693 exhibited broad-spectrum antibacterial activity. IITR00693 potentiated polymyxin B and colistin against polymyxin-resistant . IITR00693 prevented the generation of resistant mutants against multiple antibiotics. The IITR00693-polymyxin B combination decreased the count by >3 log CFU in a murine acute wound infection model. IITR00693 is a potential and promising candidate for the treatment of soft-tissue infections along with polymyxins.

摘要

抗生素耐药性在皮肤感染病原体中的出现对公共健康构成了紧迫威胁,并推动了新疗法的研究。增强现有抗生素的效力是治疗耐药病原体感染的替代方法。在这项研究中,我们旨在确定一种可以增强现有抗生素效力的小分子。新型抗菌小分子 IITR00693(2-氨基六氢嘧啶)增强了多粘菌素 B 对 和 的抗菌活性。在此,我们详细研究了这种相互作用的作用模式以及该分子对抗 和 引起的软组织感染的能力。通过微量稀释棋盘试验确定了多粘菌素 B 和 IITR00693 在 和 的临床分离株中的协同相互作用。进行时间杀伤动力学、抗生素后效应和耐药性产生研究以评估组合的药效动力学。进行基于不同荧光探针的测定以解析该组合的作用机制。在小鼠急性伤口感染模型中确定了 IITR00693-多粘菌素 B 组合的疗效。ITR00693 表现出广谱抗菌活性。ITR00693 增强了多粘菌素 B 和粘菌素对多粘菌素耐药 的作用。ITR00693 防止了针对多种抗生素的耐药突变体的产生。IITR00693-多粘菌素 B 组合在小鼠急性伤口感染模型中使 计数减少了 >3 个对数 CFU。ITR00693 是一种有前途的候选药物,可与多粘菌素一起用于治疗软组织感染。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验