Cold Stress Makes Escherichia coli Susceptible to Glycopeptide Antibiotics by Altering Outer Membrane Integrity

被引:67
作者
Stokes, Jonathan M. [1 ]
French, Shawn [1 ]
Ovchinnikova, Olga G. [2 ]
Bouwman, Catrien [2 ]
Whitfield, Chris [2 ]
Brown, Eric D. [1 ]
机构
[1] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
[2] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
ENTERICA SEROVAR TYPHIMURIUM; SALMONELLA-ENTERICA; ANTIBACTERIAL DISCOVERY; ANTIMICROBIAL PEPTIDES; PERMEABILITY BARRIER; MOLECULAR-BASIS; O-ANTIGEN; IN-VIVO; LIPOPOLYSACCHARIDE; RESISTANCE;
D O I
10.1016/j.chembiol.2015.12.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A poor understanding of the mechanisms by which antibiotics traverse the outer membrane remains a considerable obstacle to the development of novel Gram-negative antibiotics. Herein, we demonstrate that the Gram-negative bacterium Escherichia coli becomes susceptible to the narrow-spectrum antibiotic vancomycin during growth at low temperatures. Heterologous expression of an Enterococcus vanHBX vancomycin resistance cluster in E. coli confirmed that the mechanism of action was through inhibition of peptidoglycan biosynthesis. To understand the nature of vancomycin permeability, we screened for strains of E. coli that displayed resistance to vancomycin at low temperature. Surprisingly, we observed that mutations in outer membrane biosynthesis suppressed vancomycin activity. Subsequent chemical analysis of lipopolysaccharide from vancomycin-sensitive and -resistant strains confirmed that suppression was correlated with truncations in the core oligosaccharide of lipopolysaccharide. These unexpected observations challenge the current understanding of outermembrane permeability, and provide new chemical insights into the susceptibility of E. coli to glycopeptide antibiotics.
引用
收藏
页码:267 / 277
页数:11
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