Regulating polymyxin resistance in Gram-negative bacteria: roles of two-component systems PhoPQ and PmrAB

被引:63
作者
Huang, Jiayuan [1 ,2 ]
Li, Chen [1 ,3 ,4 ]
Song, Jiangning [1 ,3 ]
Velkov, Tony [5 ]
Wang, Lushan [6 ]
Zhu, Yan [1 ,2 ]
Li, Jian [1 ,2 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Melbourne, Vic 3800, Australia
[2] Monash Univ, Dept Microbiol, Melbourne, Vic 3800, Australia
[3] Monash Univ, Dept Biochem & Mol Biol, Melbourne, Vic 3800, Australia
[4] Swiss Fed Inst Technol, Dept Biol, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[5] Univ Melbourne, Fac Med Dent & Hlth Sci, Sch Biomed Sci, Dept Pharmacol & Therapeut, Melbourne, Vic 3010, Australia
[6] Shandong Univ, State Key Lab Microbial Technol, Qingdao 266237, Peoples R China
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
lipid A modification; PhoPQ; PmrAB; polymyxin resistance; two-component system; CATIONIC ANTIMICROBIAL PEPTIDES; COLISTIN-RESISTANCE; PSEUDOMONAS-AERUGINOSA; KLEBSIELLA-PNEUMONIAE; ACINETOBACTER-BAUMANNII; ESCHERICHIA-COLI; SENSOR KINASE; PHOSPHOETHANOLAMINE MODIFICATION; SALMONELLA-TYPHIMURIUM; MUTATIONAL ANALYSIS;
D O I
10.2217/fmb-2019-0322
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Polymyxins (polymyxin B and colistin) are last-line antibiotics against multidrug-resistant Gram-negative pathogens. Polymyxin resistance is increasing worldwide, with resistance most commonly regulated by two-component systems such as PmrAB and PhoPQ. This review discusses the regulatory mechanisms of PhoPQ and PmrAB in mediating polymyxin resistance, from receiving an external stimulus through to activation of genes responsible for lipid A modifications. By analyzing the reported nonsynonymous substitutions in each two-component system, we identified the domains that are critical for polymyxin resistance. Notably, for PmrB 71% of resistance-conferring nonsynonymous mutations occurred in the HAMP (present in histidine kinases, adenylate cyclases, methyl accepting proteins and phosphatase) linker and DHp (dimerization and histidine phosphotransfer) domains. These results enhance our understanding of the regulatory mechanisms underpinning polymyxin resistance and may assist with the development of new strategies to minimize resistance emergence.
引用
收藏
页码:445 / 459
页数:15
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