Staphylococcus aureus virulence factors associated with infected skin lesions: influence on the local immune response

Patricia M Mertz1, Tatiana C P Cardenas, Richard V Snyder

  • 1Miami Dermatology Research Institute, Miami, Florida, USA.

Archives of Dermatology
|October 17, 2007
PubMed
Abstract

Insights

Staphylococcus aureus skin infections show specific toxin-producing bacteria linked to white blood cell (WBC) counts. Exfoliative toxins (ETA/ETB) correlate with low WBC counts, while Panton-Valentine leukocidin (PVL) links to high counts.

Area of Science:

  • Microbiology
  • Immunology
  • Dermatology

Background:

  • Staphylococcus aureus is a common cause of skin infections.
  • Certain S. aureus strains produce toxins that can modulate the host immune response.
  • Understanding the relationship between these toxins and the host's inflammatory response is crucial for managing skin infections.

Purpose of the Study:

  • To investigate the presence of immune system-modulating toxin genes in S. aureus isolates from skin lesions.
  • To correlate the identified toxin profiles with white blood cell (WBC) counts in the infected lesions.

Main Methods:

  • Collected specimens from 105 infected skin lesions for bacterial culture and WBC counts.
  • Utilized real-time PCR to detect toxin genes (ETA, ETB, PVL, TSST) in 84 S. aureus isolates.
  • Compared toxin gene profiles between low (0-5 WBCs/LPF) and high (>5 WBCs/LPF) WBC count groups using chi-squared analysis.

Main Results:

  • A high prevalence of exfoliative toxin A/B (ETA/ETB) and Panton-Valentine leukocidin (PVL) genes was observed in S. aureus isolates, irrespective of initial WBC counts.
  • Low WBC counts were associated with ETA and ETB, whereas high WBC counts correlated with PVL and toxic shock syndrome toxin (TSST).
  • No significant differences in the clinical appearance of skin lesions were noted between the groups.

Conclusions:

  • Specific S. aureus virulence factors, including ETA, ETB, and PVL, are associated with varying WBC counts in infected skin lesions.
  • The precise mechanisms by which these toxins influence WBC counts in skin infections require further investigation.

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