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一种根除多重耐药细菌感染并减缓耐药性产生的大分子方法。

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

作者信息

Chin Willy, Zhong Guansheng, Pu Qinqin, Yang Chuan, Lou Weiyang, De Sessions Paola Florez, Periaswamy Balamurugan, Lee Ashlynn, Liang Zhen Chang, Ding Xin, Gao Shujun, Chu Collins Wenhan, Bianco Simone, Bao Chang, Tong Yen Wah, Fan Weimin, Wu Min, Hedrick James L, Yang Yi Yan

机构信息

Institute of Bioengineering and Nanotechnology, 31 Biopolis Way, Singapore, 138669, Singapore.

NUS Graduate School for Integrative Sciences and Engineering (NGS), 28 Medical Drive, Singapore, 117456, Singapore.

出版信息

Nat Commun. 2018 Mar 2;9(1):917. doi: 10.1038/s41467-018-03325-6.

DOI:10.1038/s41467-018-03325-6
PMID:29500445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5834525/
Abstract

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-ED/LD: 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.

摘要

多粘菌素仍然是治疗多重耐药(MDR)感染的最后一道防线。随着多粘菌素耐药性的出现,迫切需要开发能够缓解多重耐药的有效抗菌剂。在此,我们报告了具有独特机制且不会诱导耐药性的可生物降解胍基功能化聚碳酸酯。与传统抗生素不同,重复使用这些聚合物不会导致耐药性。对细菌的转录组分析进一步表明,经过30次处理后,细菌会对抗生素产生耐药性,但对这些大分子不会产生耐药性。重要的是,在多重耐药鲍曼不动杆菌、大肠杆菌、肺炎克雷伯菌、耐甲氧西林金黄色葡萄球菌、盲肠结扎和穿刺诱导的多微生物腹膜炎以及铜绿假单胞菌肺部感染小鼠模型中,这些大分子在体内具有很高的治疗效果,同时保持无毒(例如,鲍曼不动杆菌感染的治疗指数-ED/LD:1473)。这些可生物降解的合成大分子已被证明在体内具有广谱抗菌活性,作为针对多重耐药感染的全身性抗菌剂具有极好的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/1ef62157674f/41467_2018_3325_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/207b21556228/41467_2018_3325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/de9e66eb4b00/41467_2018_3325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/01cba6e858da/41467_2018_3325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/c1bce41a3b9c/41467_2018_3325_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/755a7f754ea8/41467_2018_3325_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/9b5e15f19980/41467_2018_3325_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/1ef62157674f/41467_2018_3325_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/207b21556228/41467_2018_3325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/de9e66eb4b00/41467_2018_3325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/01cba6e858da/41467_2018_3325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/c1bce41a3b9c/41467_2018_3325_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/755a7f754ea8/41467_2018_3325_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/9b5e15f19980/41467_2018_3325_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c8/5834525/1ef62157674f/41467_2018_3325_Fig7_HTML.jpg

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