Probing the Penetration of Antimicrobial Polymyxin Lipopeptides into Gram-Negative Bacteria

被引:111
作者
Deris, Zakuan Z. [1 ,3 ]
Swarbrick, James D. [2 ]
Roberts, Kade D. [2 ]
Azad, Mohammad A. K. [1 ]
Akter, Jesmin [1 ]
Horne, Andrew S. [2 ]
Nation, Roger L. [1 ]
Rogers, Kelly L. [4 ]
Thompson, Phillip E. [2 ]
Velkov, Tony [1 ]
Li, Jian [1 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Melbourne, Vic 3800, Australia
[2] Monash Univ, Monash Inst Pharmaceut Sci, Dept Med Chem, Melbourne, Vic 3800, Australia
[3] Univ Sains Malaysia, Sch Med Sci, Dept Med Microbiol & Parasitol, Kubang Kerian 16150, Kelantan, Malaysia
[4] Walter & Eliza Hall Inst Med Res, Ctr Dynam Imaging, Parkville, Vic 3052, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
RESISTANT ACINETOBACTER-BAUMANNII; INFECTIOUS-DISEASES-SOCIETY; IN-VITRO PHARMACODYNAMICS; PSEUDOMONAS-AERUGINOSA; KLEBSIELLA-PNEUMONIAE; MULTIDRUG-RESISTANCE; B NONAPEPTIDE; OUTER-MEMBRANE; PEPTIDE RESISTANCE; COLISTIN;
D O I
10.1021/bc500094d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The dry antibiotic development pipeline coupled with the emergence of multidrug resistant Gram-negative 'superbugs' has driven the revival of the polymyxin lipopeptide antibiotics. Polymyxin resistance implies a total lack of antibiotics for the treatment of life-threatening infections. The lack of molecular imaging probes that possess native polymyxin-like antibacterial activity is a barrier to understanding the resistance mechanisms and the development of a new generation of polymyxin lipopeptides. Here we report the regioselective modification of the polymyxin B core scaffold at the N-terminus with the dansyl fluorophore to generate an active probe that mimics polymyxin B pharmacologically. Time-lapse laser scanning confocal microscopy imaging of the penetration of probe (1) into Gram-negative bacterial cells revealed that the probe initially accumulates in the outer membrane and subsequently penetrates into the inner membrane and finally the cytoplasm. The implementation of this polymyxin-mimetic probe will advance the development of platforms for the discovery of novel polymyxin lipopeptides with efficacy against polymyxin-resistant strains.
引用
收藏
页码:750 / 760
页数:11
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