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How do bacteria resist human antimicrobial peptides?
Ist Teil von
Trends in Microbiology, 2002-04, Vol.10 (4), p.179-186
Ort / Verlag
England: Elsevier Ltd
Erscheinungsjahr
2002
Link zum Volltext
Quelle
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
Beschreibungen/Notizen
Cationic antimicrobial peptides (CAMPs), such as defensins, cathelicidins and thrombocidins, are an important human defense mechanism, protecting skin and epithelia against invading microorganisms and assisting neutrophils and platelets.
Staphylococcus aureus,
Salmonella enterica and other bacterial pathogens have evolved countermeasures to limit the effectiveness of CAMPs, including the repulsion of CAMPs by reducing the net negative charge of the bacterial cell envelope through covalent modification of anionic molecules (e.g. teichoic acids, phospholipids and lipid A); expelling CAMPs through energy-dependent pumps; altering membrane fluidity; and cleaving CAMPs with proteases. Mutants susceptible to CAMPs are more efficiently inactivated by phagocytes and are virulence-attenuated, indicating that CAMP resistance plays a key role in bacterial infections.
The efficacy of cationic antimicrobial peptides, ‘natural antibiotics’ of the innate immune system, is limited by a variety of sophisticated microbial mechanisms that have recently attracted increasing interest.