Abstract
Background:
Staphylococcus epidermidis, a commensal skin pathogen, is a key pathogen in surgical site infections (SSIs). This study characterized clinical isolates obtained from an abdominal operation to guide decolonization therapy.
Methods:
In total, 146 S. epidermidis isolates obtained from pre-operative skin swabs of patients undergoing gynecological procedures were analyzed. PCR was performed to detect mecA, efflux pump genes (qacA/B, smr, etc.), and biofilm-associated genes (icaA-D, aap). Methicillin-resistant S. epidermidis (MRSE) isolates were typed by multi-locus sequence typing. Broth microdilution was used to assess susceptibility to benzalkonium chloride (BAC) and chlorhexidine digluconate (CHG). Biofilm formation was measured in the presence or absence of sub-inhibitory antiseptic exposure.
Results:
Of the isolates, 49.3% were MRSE, and 63.0% and 29.5% carried qacA/B and smr, respectively. MRSE showed higher minimum inhibitory concentration (MIC50) values for both antiseptics. qac-positive strains exhibited significantly increased BAC MIC50 (1 vs. 0.25 µg/mL; p < 0.001). Biofilm-forming isolates (16.4%) had three-fold higher BAC MIC50 (p < 0.01). Sub-MIC exposure to BAC/CHG induced biofilm formation in prior non-producers (p < 0.05); among these, 81.3% were qac-positive, and 62.5% were MRSE.
Conclusions:
The high prevalence of MRSE and efflux genes contributed to antiseptic tolerance. Sub-inhibitory antiseptic concentrations may enhance biofilm formation in resistant strains, underscoring the need for optimized decolonization tactics to prevent SSI.
Keywords
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