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Acapsular clinical Staphylococcus aureus isolates lack agr function.

J Fischer1, J C Lee, G Peters

  • 1Institute of Medical Microbiology, University Hospital Münster, Münster, Germany; The Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|November 15, 2013
PubMed
Summary
This summary is machine-generated.

Staphylococcus aureus strains with a non-functional accessory gene regulator (agr) system were less likely to produce capsular polysaccharide (CP). This suggests agr influences CP expression in clinical isolates.

Keywords:
Staphylococcus aureusagrcapsuleclinical isolatesvirulence

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Area of Science:

  • Microbiology
  • Infectious Diseases
  • Molecular Biology

Background:

  • Staphylococcus aureus is a significant cause of bacterial infections.
  • Capsular polysaccharide (CP) aids S. aureus in evading host defenses.
  • The accessory gene regulator (agr) system controls virulence factors in S. aureus.

Purpose of the Study:

  • To investigate the relationship between capsular polysaccharide (CP) expression and accessory gene regulator (agr) activity in clinical Staphylococcus aureus isolates.
  • To determine if agr functionality impacts CP production in patient-derived S. aureus strains.

Main Methods:

  • Assessed CP production and agr expression in 195 clinical S. aureus isolates.
  • Utilized Northern blot analysis to evaluate agr locus functionality and CP expression.

Main Results:

  • A notable association was found between agr functionality and CP production.
  • S. aureus strains with a non-functional agr locus were significantly more likely to be CP-negative.
  • Conversely, strains with a functional agr locus showed a higher propensity for CP production.

Conclusions:

  • The accessory gene regulator (agr) system appears to play a role in regulating capsular polysaccharide (CP) expression in clinical S. aureus isolates.
  • Understanding this interaction may offer new insights into S. aureus pathogenesis and treatment strategies.