多粘菌素
微生物学
抗菌剂
多糖
多粘菌素B
革兰氏阴性菌
细菌
细胞毒性
脂质A
细菌外膜
肺炎克雷伯菌
抗生素
生物
化学
体外
生物化学
大肠杆菌
遗传学
基因
作者
Xiangfeng Lai,Seong Hoong Chow,Anton P. Le Brun,Benjamin W. Muir,Phillip J. Bergen,John White,Heidi H. Yu,Jiping Wang,Jill Danne,Jhih‐Hang Jiang,Francesca L. Short,Mei‐Ling Han,Richard A. Strugnell,Jiangning Song,Neil R. Cameron,Anton Y. Peleg,Jian Li,Hsin‐Hui Shen
出处
期刊:Small
[Wiley]
日期:2023-10-05
卷期号:20 (6)
被引量:1
标识
DOI:10.1002/smll.202305052
摘要
The rapid increase and spread of Gram-negative bacteria resistant to many or all existing treatments threaten a return to the preantibiotic era. The presence of bacterial polysaccharides that impede the penetration of many antimicrobials and protect them from the innate immune system contributes to resistance and pathogenicity. No currently approved antibiotics target the polysaccharide regions of microbes. Here, describe monolaurin-based niosomes, the first lipid nanoparticles that can eliminate bacterial polysaccharides from hypervirulent Klebsiella pneumoniae, are described. Their combination with polymyxin B shows no cytotoxicity in vitro and is highly effective in combating K. pneumoniae infection in vivo. Comprehensive mechanistic studies have revealed that antimicrobial activity proceeds via a multimodal mechanism. Initially, lipid nanoparticles disrupt polysaccharides, then outer and inner membranes are destabilized and destroyed by polymyxin B, resulting in synergistic cell lysis. This novel lipidic nanoparticle system shows tremendous promise as a highly effective antimicrobial treatment targeting multidrug-resistant Gram-negative pathogens.
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