Townsend E C, Xu K, De La Cruz K, Huang L, Sandstrom S, Meudt J J, Shanmuganayagam D, Huttenlocher A, Gibson A L F, Kalan L R
Department of Medical Microbiology and Immunology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Microbiology Doctoral Training Program, University of Wisconsin-Madison, Madison, Wisconsin, USA.
mSphere. 2025 Sep 30;10(9):e0044125. doi: 10.1128/msphere.00441-25. Epub 2025 Aug 28.
Incomplete antiseptic efficacy against potentially pathogenic microbial taxa places some patients at disproportionate risk for developing a surgical site infection. Laboratory models capable of interrogating the effects of antiseptics on the skin and its complex microbial communities are desperately needed to improve and better tailor antiseptic formulations. This work aims to establish an porcine skin model to explore the impact of topical antiseptics on complex skin microbial communities and superficial skin lipids. Microbiome samples were treated with propidium monoazide to selectively evaluate DNA from viable microorganisms. Bacterial abundances were assessed via viability-qPCR and quantitative culture. Viable community populations were evaluated with 16S rRNA gene sequencing. Epidermal biopsies were collected at multiple time points for lipidomic assessment via LC/MS. The environment promoted shifts in porcine skin lipid composition and microbial communities over the experiment's duration. Compared to water-treated control skin, skin treated with the antiseptic chlorhexidine gluconate had significantly lower culturable counts and bioburden as determined by viability-qPCR. Compared to water-treated skin, viable microbial communities on CHG-treated skin displayed greater relative abundance of several gut-associated and Gram-negative bacterial taxa, including , , , and . Collectively, these findings highlight the utility of an porcine skin system for interrogating the impacts of antimicrobial disruption on complex microbial ecosystems, and ultimately, for the future testing and development of improved antiseptic formulations.
Broad-spectrum antiseptics are widely used to prevent surgical site infection and as wound cleansing agents. The impacts of such agents on beneficial microbes in the skin microbiome are understudied. Here, we describe an skin model to test the impacts of antiseptics or other topical agents on the healthy skin microbiome.
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