...
首页> 外文期刊>Nature Communications >A macromolecular approach to eradicate multidrug resistant bacterial infections while mitigating drug resistance onset
【24h】

A macromolecular approach to eradicate multidrug resistant bacterial infections while mitigating drug resistance onset

机译:消除多药耐药性细菌感染同时减轻耐药性发作的大分子方法

获取原文
           

摘要

Polymyxins remain the last line treatment for multidrug-resistant (MDR) infections. As polymyxins resistance emerges, there is an urgent need to develop effective antimicrobial agents capable of mitigating MDR. Here, we report biodegradable guanidinium-functionalized polycarbonates with a distinctive mechanism that does not induce drug resistance. Unlike conventional antibiotics, repeated use of the polymers does not lead to drug resistance. Transcriptomic analysis of bacteria further supports development of resistance to antibiotics but not to the macromolecules after 30 treatments. Importantly, high in vivo treatment efficacy of the macromolecules is achieved in MDR A. baumannii-, E. coli-, K. pneumoniae-, methicillin-resistant S. aureus-, cecal ligation and puncture-induced polymicrobial peritonitis, and P. aeruginosa lung infection mouse models while remaining non-toxic (e.g., therapeutic index—ED50/LD50: 1473 for A. baumannii infection). These biodegradable synthetic macromolecules have been demonstrated to have broad spectrum in vivo antimicrobial activity, and have excellent potential as systemic antimicrobials against MDR infections.
机译:多粘菌素仍然是耐多药(MDR)感染的最后治疗方法。随着多粘菌素耐药性的出现,迫切需要开发能够减轻MDR的有效抗菌剂。在这里,我们报告具有独特机制且不引起耐药性的可生物降解的胍基官能化聚碳酸酯。与常规抗生素不同,重复使用聚合物不会导致耐药性。细菌的转录组学分析进一步支持了对抗生素的抗药性发展,但对30种处理后的大分子无抗药性。重要的是,在耐多药鲍曼不动杆菌,大肠杆菌,肺炎克雷伯氏菌,耐甲氧西林的金黄色葡萄球菌,盲肠结扎和穿刺诱导的微生物性腹膜炎和铜绿假单胞菌中,可以获得大分子的高体内治疗功效。肺部感染小鼠模型,同时保持无毒(例如,鲍曼不动杆菌感染的治疗指数-ED50 / LD50:1473)。这些可生物降解的合成大分子已被证明具有广谱的体内抗菌活性,并且具有作为对抗MDR感染的系统性抗菌剂的极好的潜力。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号