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Inoculation of Staphylococcus xylosus in SJL/J mice to determine pathogenicity

Venita B Thornton1, Judith A Davis, Mark B St Clair

  • 1Uniformed Services University of the Health Sciences (USUHS), 4301 Jones Bridge Road, Bethesda, MD 20814, USA.

Contemporary Topics in Laboratory Animal Science
|August 9, 2003
PubMed

Insights

Staphylococcus xylosus, a nonpathogenic bacterium, caused skin lesions in mice. Treatment with Sulfamethoxazole-Trimethoprim resolved these experimental cutaneous lesions, demonstrating therapeutic efficacy.

Area of Science:

  • Microbiology
  • Dermatology
  • Infectious Diseases

Background:

  • Staphylococcus xylosus is typically a nonpathogenic commensal bacterium.
  • It is rarely implicated in causing infections in mammals.
  • Previous research has not extensively documented its pathogenic potential.

Purpose of the Study:

  • To investigate the pathogenicity of Staphylococcus xylosus.
  • To determine if intradermal tail inoculation causes lesions in SJL/J mice.
  • To evaluate the efficacy of Sulfamethoxazole-Trimethoprim in treating induced lesions.

Main Methods:

  • SJL/J mice were inoculated intradermally in the tail with Staphylococcus xylosus.
  • Inoculation involved silk sutures impregnated with bacteria and superficial abrasion.
  • Lesions were monitored, and bacterial recovery was performed. Treatment group received Sulfamethoxazole-Trimethoprim in drinking water.

Main Results:

  • Approximately 80% of inoculated mice developed cutaneous tail lesions.
  • Staphylococcus xylosus was successfully recovered from the induced lesions.
  • Sulfamethoxazole-Trimethoprim treatment led to the resolution of lesions in treated mice.

Conclusions:

  • Staphylococcus xylosus can induce pathologic cutaneous lesions in SJL/J mice.
  • Experimental S. xylosus infection in mice is treatable with Sulfamethoxazole-Trimethoprim.
  • This study highlights a potential pathogenic role for S. xylosus under specific experimental conditions.

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