Polysaccharide-Targeting Lipid Nanoparticles to Kill Gram-Negative Bacteria.
Xiangfeng LaiSeong Hoong ChowAnton P Le BrunBenjamin W MuirPhillip J BergenJacinta WhiteHeidi H YuJiping WangJill DanneJhih-Hang JiangFrancesca L ShortMei-Ling HanRichard A StrugnellJiangning SongNeil R CameronAnton Y PelegJian LiHsin-Hui ShenPublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
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.
Keyphrases
- gram negative
- multidrug resistant
- klebsiella pneumoniae
- drug resistant
- acinetobacter baumannii
- water soluble
- cancer therapy
- single cell
- fatty acid
- immune response
- staphylococcus aureus
- walled carbon nanotubes
- big data
- stem cells
- cell therapy
- combination therapy
- machine learning
- artificial intelligence
- biofilm formation
- loop mediated isothermal amplification
- bone marrow
- replacement therapy
- iron oxide
- drug administration