The staphylococcal protease SspA perturbs the epidermal barrier and promotes IL-22-driven inflammation in allergen-exposed skin

Skin colonization by Staphylococcus aureus has emerged as a common feature of atopic dermatitis and other allergic diseases, yet it remains unclear how this bacterium contributes to inflammation and pathology. Our S. aureus secretome analysis and bioactivity-guided fractionation uncover that the serine protease SspA destroys keratinocyte junctions, increases epidermal permeability, and activates an epithelial inflammatory program linked to barrier dysfunction. SspA and house dust mite extract (HDM), when epicutaneously applied in combination, cause interleukin (IL)-22-dependent atopic dermatitis-like skin disease in mice. Spatial single-cell analysis and immunophenotyping of lesional skin of these mice reveal massive elongation and branching of epidermal nerve fibers and the formation of T cells simultaneously producing IL-13 and IL-22. Chemical denervation and the resultant dismantling of the neuroimmune signaling network reverse the pathology driven by SspA–HDM combination. These findings link S. aureus colonization to barrier perturbation, allergen sensitization, and neurogenic dermatitis.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-10-28
DOI
https://doi.org/10.1073/pnas.2611563123
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

The staphylococcal protease SspA perturbs the epidermal barrier and promotes IL-22-driven inflammation in allergen-exposed skin

Juan Miguel Jiménez‐Andrade, Katia Georgopoulos, Lindsey Neil Shaw, Jin Mo Park et al.
1 links
Proceedings of the National Academy of Sciences
Dermatology and Skin Diseases
article

The staphylococcal protease SspA perturbs the epidermal barrier and promotes IL-22-driven inflammation in allergen-exposed skin

Juan Miguel Jiménez‐Andrade, Katia Georgopoulos, Lindsey Neil Shaw, Jin Mo Park, Toshimi Yoshida, Kevin S. Wei, Juan Antonio Vazquez-Mora, Yanek Jiménez-Andrade, Ethan A. Lerner, Kathryn R. Hillette, Stefano Sol, Anna Mandinova, Miles Tran, Lilah Gmyrek
article en

Abstract

Skin colonization by Staphylococcus aureus has emerged as a common feature of atopic dermatitis and other allergic diseases, yet it remains unclear how this bacterium contributes to inflammation and pathology. Our S. aureus secretome analysis and bioactivity-guided fractionation uncover that the serine protease SspA destroys keratinocyte junctions, increases epidermal permeability, and activates an epithelial inflammatory program linked to barrier dysfunction. SspA and house dust mite extract (HDM), when epicutaneously applied in combination, cause interleukin (IL)-22-dependent atopic dermatitis-like skin disease in mice. Spatial single-cell analysis and immunophenotyping of lesional skin of these mice reveal massive elongation and branching of epidermal nerve fibers and the formation of T cells simultaneously producing IL-13 and IL-22. Chemical denervation and the resultant dismantling of the neuroimmune signaling network reverse the pathology driven by SspA–HDM combination. These findings link S. aureus colonization to barrier perturbation, allergen sensitization, and neurogenic dermatitis.

Proceedings of the National Academy of SciencesVol. 123(44)
Broad Institute (US), Brigham and Women's Hospital (US), Harvard University (US), University of South Florida (US), Massachusetts General Hospital (US), Harvard Stem Cell Institute (US), International Research Center for Medical Sciences, Kumamoto University (JP), Autonomous University of Tamaulipas (MX), Kumamoto University (JP)
U.S. Department of Defense, National Institute of Allergy and Infectious Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Good health and well-being
Openalex Percentile: Top 10%
Dermatology and Skin Diseases
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