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• W2071176300 abstract "PSMs are a recently discovered family of short, amphipathic, α-helical peptides in staphylococci. Several PSMs are key virulence determinants, particularly in highly virulent Staphylococcus aureus strains. PSMα peptides of S. aureus facilitate neutrophil lysis after phagocytosis, and are key contributors to several infection types, including skin infection and bacteremia. Furthermore, all PSMs contribute to biofilm structuring and the dissemination of biofilm-associated infection. Cytolytic PSMs as produced by S. aureus appear to have evolved from original functions in the non-infectious lifestyle of staphylococci. The surfactant properties of PSMs, which they all share, are believed to facilitate growth on epithelial surfaces. The basic role of PSMs in staphylococcal physiology is underscored, for example, by their exceptionally strict and direct control by quorum-sensing and the presence of a dedicated secretion system. Targeting PSMs for anti-staphylococcal drug development may be a promising approach to overcome the problems associated with widespread antibiotic resistance in staphylococci." @default.
• W2071176300 created "2016-06-24" @default.
• W2071176300 creator A5056173398 @default.
• W2071176300 date "2014-03-01" @default.
• W2071176300 modified "2023-10-14" @default.
• W2071176300 title "Phenol-soluble modulins" @default.
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• W2071176300 doi "https://doi.org/10.1016/j.ijmm.2013.11.019" @default.
• W2071176300 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4014003" @default.
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