Literature DB >> 24447915

Phenol-soluble modulins.

Michael Otto1.   

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. Published by Elsevier GmbH.

Entities:  

Keywords:  Biofilm; Cytolysis; Leukotoxin; Neutrophils; Phenol-soluble modulins; Staphylococcus aureus; Staphylococcus epidermidis; Toxins

Mesh:

Substances:

Year:  2013        PMID: 24447915      PMCID: PMC4014003          DOI: 10.1016/j.ijmm.2013.11.019

Source DB:  PubMed          Journal:  Int J Med Microbiol        ISSN: 1438-4221            Impact factor:   3.473


  67 in total

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Authors:  W E Kloos; M S Musselwhite
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9.  Phenol-soluble modulins in staphylococci: What are they originally for?

Authors:  Saravanan Periasamy; Som S Chatterjee; Gordon Y C Cheung; Michael Otto
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  61 in total

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Authors:  Korbin H J West; Wenqi Shen; Emma L Eisenbraun; Tian Yang; Joseph K Vasquez; Alexander R Horswill; Helen E Blackwell
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2.  Use of a Stereochemical Strategy To Probe the Mechanism of Phenol-Soluble Modulin α3 Toxicity.

Authors:  Zhihui Yao; Brian P Cary; Craig A Bingman; Chenxuan Wang; Dale F Kreitler; Kenneth A Satyshur; Katrina T Forest; Samuel H Gellman
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Review 3.  Host-Pathogen Interactions in Gram-Positive Bacterial Pneumonia.

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Journal:  Clin Microbiol Rev       Date:  2019-05-29       Impact factor: 26.132

4.  Survival of Staphylococcus epidermidis in Fibroblasts and Osteoblasts.

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5.  Mass spectrometric identification of phenol-soluble modulins in the ATCC® 43300 standard strain of methicillin-resistant Staphylococcus aureus harboring two distinct phenotypes.

Authors:  K S Jang; M Park; J Y Lee; J S Kim
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2017-01-14       Impact factor: 3.267

6.  Subinhibitory Concentrations of Mupirocin Stimulate Staphylococcus aureus Biofilm Formation by Upregulating cidA.

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7.  Conformational Switch to a β-Turn in a Staphylococcal Quorum Sensing Signal Peptide Causes a Dramatic Increase in Potency.

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8.  Structure-Function Analyses of a Staphylococcus epidermidis Autoinducing Peptide Reveals Motifs Critical for AgrC-type Receptor Modulation.

Authors:  Tian Yang; Yftah Tal-Gan; Alexandra E Paharik; Alexander R Horswill; Helen E Blackwell
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9.  Modulation of Staphylococcus aureus Biofilm Matrix by Subinhibitory Concentrations of Clindamycin.

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10.  Increased in vitro phenol-soluble modulin production is associated with soft tissue infection source in clinical isolates of methicillin-susceptible Staphylococcus aureus.

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Journal:  J Infect       Date:  2016-01-09       Impact factor: 6.072

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