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      Adhesion of Staphylococcus aureus to Corneocytes from Atopic Dermatitis Patients Is Controlled by Natural Moisturizing Factor Levels

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          ABSTRACT

          The bacterial pathogen Staphylococcus aureus plays an important role in atopic dermatitis (AD), a chronic disorder that mostly affects children. Colonization of the skin of AD patients by S. aureus exacerbates the disease, but the molecular determinants of the bacterium-skin adhesive interactions are poorly understood. Specifically, reduced levels of natural moisturizing factor (NMF) in the stratum corneum have been shown to be associated with more severe AD symptoms, but whether this is directly related to S. aureus adhesion is still an open question. Here, we demonstrate a novel relationship between NMF expression in AD skin and strength of bacterial adhesion. Low-NMF corneocytes, unlike high-NMF ones, are covered by a dense layer of nanoscale villus protrusions. S. aureus bacteria isolated from AD skin bind much more strongly to corneocytes when the NMF level is reduced. Strong binding forces originate from a specific interaction between the bacterial adhesion clumping factor B (ClfB) and skin ligands. Remarkably, mechanical tension dramatically strengthens ClfB-mediated adhesion, as observed with catch bonds, demonstrating that physical stress plays a role in promoting colonization of AD skin by S. aureus. Collectively, our findings demonstrate that patient NMF levels regulate the strength of S. aureus-corneocyte adhesion, the first step in skin colonization, and suggest that the ClfB binding mechanism could represent a potential target for new therapeutic treatments.

          IMPORTANCE

          Bacterium-skin interactions play important roles in skin disorders, yet their molecular details are poorly understood. In this study, we decipher the molecular forces at play during adhesion of Staphylococcus aureus to skin corneocytes in the clinically important context of atopic dermatitis (AD), also known as eczema. We identify a unique relationship between the level of natural moisturizing factor (NMF) in the skin and the strength of bacterium-corneocyte adhesion. Bacterial adhesion is primarily mediated by the surface protein clumping factor B (ClfB) and is enhanced by physical stress, highlighting the role of protein mechanobiology in skin colonization. Similar to a catch bond behavior, this mechanism represents a promising target for the development of novel antistaphylococcal agents.

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          Most cited references32

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          Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.

          Atopic disease, including atopic dermatitis (eczema), allergy and asthma, has increased in frequency in recent decades and now affects approximately 20% of the population in the developed world. Twin and family studies have shown that predisposition to atopic disease is highly heritable. Although most genetic studies have focused on immunological mechanisms, a primary epithelial barrier defect has been anticipated. Filaggrin is a key protein that facilitates terminal differentiation of the epidermis and formation of the skin barrier. Here we show that two independent loss-of-function genetic variants (R510X and 2282del4) in the gene encoding filaggrin (FLG) are very strong predisposing factors for atopic dermatitis. These variants are carried by approximately 9% of people of European origin. These variants also show highly significant association with asthma occurring in the context of atopic dermatitis. This work establishes a key role for impaired skin barrier function in the development of atopic disease.
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            Filaggrin mutations associated with skin and allergic diseases.

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              Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

              Ichthyosis vulgaris (OMIM 146700) is the most common inherited disorder of keratinization and one of the most frequent single-gene disorders in humans. The most widely cited incidence figure is 1 in 250 based on a survey of 6,051 healthy English schoolchildren. We have identified homozygous or compound heterozygous mutations R501X and 2282del4 in the gene encoding filaggrin (FLG) as the cause of moderate or severe ichthyosis vulgaris in 15 kindreds. In addition, these mutations are semidominant; heterozygotes show a very mild phenotype with incomplete penetrance. The mutations show a combined allele frequency of approximately 4% in populations of European ancestry, explaining the high incidence of ichthyosis vulgaris. Profilaggrin is the major protein of keratohyalin granules in the epidermis. During terminal differentiation, it is cleaved into multiple filaggrin peptides that aggregate keratin filaments. The resultant matrix is cross-linked to form a major component of the cornified cell envelope. We find that loss or reduction of this major structural protein leads to varying degrees of impaired keratinization.
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                Author and article information

                Contributors
                Role: Invited Editor
                Role: Editor
                Journal
                mBio
                MBio
                mbio
                mbio
                mBio
                mBio
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2150-7511
                14 August 2018
                Jul-Aug 2018
                : 9
                : 4
                : e01184-18
                Affiliations
                [a ]Institute of Life Sciences, Université Catholique de Louvain, Louvain-la-Neuve, Belgium
                [b ]National Children’s Research Centre, Our Lady’s Children’s Hospital, Dublin, Ireland
                [c ]Pediatric Dermatology, Our Lady’s Children’s Hospital, Dublin, Ireland
                [d ]Clinical Medicine, Trinity College Dublin, Dublin, Ireland
                [e ]Coronel Institute of Occupational Health, Academic Medical Center, Amsterdam, The Netherlands
                [f ]Department of Microbiology, Moyne Institute of Preventive Medicine, School of Genetics and Microbiology, Trinity College Dublin, Dublin, Ireland
                [g ]Walloon Excellence in Life Sciences and Biotechnology (WELBIO), Wavre, Belgium
                University of California, Berkeley
                University of Washington
                Author notes
                Address correspondence to Alan D. Irvine, irvinea@ 123456tcd.ie , Joan A. Geoghegan, geoghegj@ 123456tcd.ie , or Yves F. Dufrêne, Yves.Dufrene@ 123456uclouvain.be .

                C.F. and P.V. contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-3788-0668
                Article
                mBio01184-18
                10.1128/mBio.01184-18
                6094479
                30108169
                61d5d23c-b1a4-41a8-a5ca-a6e75e0a895e
                Copyright © 2018 Feuillie et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 29 May 2018
                : 6 July 2018
                Page count
                supplementary-material: 5, Figures: 7, Tables: 0, Equations: 0, References: 35, Pages: 11, Words: 6422
                Funding
                Funded by: European research concil;
                Award ID: 693630
                Award Recipient : Award Recipient : Award Recipient :
                Funded by: FNRS-WELBIO;
                Award ID: 2015A-05
                Award Recipient : Award Recipient : Award Recipient :
                Funded by: Concerted Research Action;
                Award Recipient : Award Recipient : Award Recipient :
                Funded by: FNRS;
                Award Recipient : Award Recipient : Award Recipient :
                Categories
                Research Article
                Custom metadata
                July/August 2018

                Life sciences
                adhesion,atopic dermatitis,biofilms,skin,staphylococcus aureus
                Life sciences
                adhesion, atopic dermatitis, biofilms, skin, staphylococcus aureus

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