Bacterial resistance mechanisms against host defense peptides

被引:112
|
作者
Koprivnjak, Tomaz [1 ]
Peschel, Andreas [2 ]
机构
[1] Natl Inst Chem Slovenia, Dept Biotechnol, Ljubljana 1000, Slovenia
[2] Univ Tubingen, Cellular & Mol Microbiol Sect, Interfac Inst Microbiol & Infect Med, D-72076 Tubingen, Germany
关键词
Pathogens; Cationic peptides; Teichoic acids; Lipid A; D-alanylation; Aminoarabinose; Ethanolamine; Multidrug efflux pumps; Proteases; CATIONIC ANTIMICROBIAL PEPTIDES; PLATELET MICROBICIDAL PROTEIN; STAPHYLOCOCCUS-AUREUS STRAINS; IN-VITRO RESISTANCE; WALL TEICHOIC-ACID; POLYSACCHARIDE INTERCELLULAR ADHESIN; ALANYL-LIPOTEICHOIC ACID; OUTER-MEMBRANE PROTEASE; IIA PHOSPHOLIPASE A(2); D-ALANINE;
D O I
10.1007/s00018-011-0716-4
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
Host defense peptides and proteins are important components of the innate host defense against pathogenic microorganisms. They target negatively charged bacterial surfaces and disrupt microbial cytoplasmic membranes, which ultimately leads to bacterial destruction. Throughout evolution, pathogens devised several mechanisms to protect themselves from deleterious damage of host defense peptides. These strategies include (a) inactivation and cleavage of host defense peptides by production of host defense binding proteins and proteases, (b) repulsion of the peptides by alteration of pathogen's surface charge employing modifications by amino acids or amino sugars of anionic molecules (e.g., teichoic acids, lipid A and phospholipids), (c) alteration of bacterial membrane fluidity, and (d) expulsion of the peptides using multi drug pumps. Together with bacterial regulatory network(s) that regulate expression and activity of these mechanisms, they represent attractive targets for development of novel antibacterials.
引用
收藏
页码:2243 / 2254
页数:12
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