Staphylococcus aureus infection on cut wounds in the mouse skin: experimental staphylococcal botryomycosis

H Akiyama1, H Kanzaki, J Tada

  • 1Department of Dermatology, Okayama University Medical School, Japan.

Insights

Staphylococcus aureus can form biofilms in skin wounds of immunosuppressed mice. These bacterial structures, encased in protective layers, trigger inflammation and tissue damage over time.

Area of Science:

  • Microbiology
  • Immunology
  • Dermatology

Background:

  • Staphylococcus aureus is a common pathogen causing skin infections.
  • Neutropenia, a condition of low white blood cell count, increases susceptibility to infections.
  • Biofilm formation by bacteria contributes to persistent and difficult-to-treat infections.

Purpose of the Study:

  • To investigate the in vivo behavior of Staphylococcus aureus in a neutropenic mouse wound model.
  • To characterize the early stages of bacterial colonization and host response.
  • To determine if Staphylococcus aureus forms biofilm-like structures in dermal and subcutaneous tissues.

Main Methods:

  • Cutaneous wounds were created on cyclophosphamide-treated (neutropenic) mice.
  • Staphylococcus aureus was inoculated onto the wounds.
  • Biopsy specimens were collected at various time points (1-60 hours post-inoculation).
  • Light and electron microscopy were used for examination.
  • Ruthenium red staining was employed to detect extracellular matrix components.

Main Results:

  • Staphylococcus aureus colonized wounds and subcutaneous tissue within 1 hour.
  • Bacterial clusters formed by 6 hours.
  • Fibril-like and membrane-like structures surrounding bacteria were observed by 1 and 3 hours, respectively.
  • These structures stained positive with Ruthenium red, indicating extracellular matrix.
  • Inflammatory cells infiltrated by 36 hours.
  • Tissue degeneration and necrosis were evident by 60 hours.

Conclusions:

  • Staphylococcus aureus can form biofilm-like structures in vivo in a neutropenic host.
  • These structures appear to protect bacteria from host immune cells.
  • The findings suggest a potential mechanism for persistent S. aureus wound infections in immunocompromised individuals.