Multi‐drug resistant Staphylococcus epidermidis from chronic wounds impair healing in human wound model

Venous leg ulcers (VLUs) represent one of the most prevalent types of chronic wounds characterised by perturbed microbiome and biofilm‐forming bacteria. As one of the most abundant skin‐commensal, Staphylococcus epidermidis is known as beneficial for the host, however, some strains can form biofilms...

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Veröffentlicht in:Wound repair and regeneration 2024-11, Vol.32 (6), p.799-810
Hauptverfasser: Dinić, Miroslav, Verpile, Rebecca, Burgess, Jamie L., Ming, Jingjing, Marjanovic, Jelena, Beliz, Carmen Nicole, Plano, Lisa, Hower, Suzanne, Thaller, Seth R., Banerjee, Santanu, Lev‐Tov, Hadar, Tomic‐Canic, Marjana, Pastar, Irena
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container_end_page 810
container_issue 6
container_start_page 799
container_title Wound repair and regeneration
container_volume 32
creator Dinić, Miroslav
Verpile, Rebecca
Burgess, Jamie L.
Ming, Jingjing
Marjanovic, Jelena
Beliz, Carmen Nicole
Plano, Lisa
Hower, Suzanne
Thaller, Seth R.
Banerjee, Santanu
Lev‐Tov, Hadar
Tomic‐Canic, Marjana
Pastar, Irena
description Venous leg ulcers (VLUs) represent one of the most prevalent types of chronic wounds characterised by perturbed microbiome and biofilm‐forming bacteria. As one of the most abundant skin‐commensal, Staphylococcus epidermidis is known as beneficial for the host, however, some strains can form biofilms and hinder wound healing. In this study, S. epidermidis distribution in VLUs and associated resistome were analysed in ulcer tissue from patients. Virulence of S. epidermidis isolates from VLUs were evaluated by whole genome sequencing, antimicrobial susceptibility testing, in vitro biofilm and binding assays, and assessment of biofilm‐forming capability and pro‐inflammatory potential using human ex vivo wound model. We demonstrated that S. epidermidis isolates from VLUs inhibit re‐epithelialization through biofilm‐dependent induction of IL‐1β, IL‐8, and IL‐6 which was in accordance with impaired healing outcomes observed in patients. High extracellular matrix binding ability of VLU isolates was associated with antimicrobial resistance and expression levels of the embp and sdrG, responsible for bacterial binding to fibrinogen and fibrin, respectively. Finally, we showed that S. epidermidis from VLUs demonstrate pathogenic features with ability to impair healing which underscores the emergence of treatment‐resistant virulent lineages in patients with chronic ulcers.
doi_str_mv 10.1111/wrr.13231
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As one of the most abundant skin‐commensal, Staphylococcus epidermidis is known as beneficial for the host, however, some strains can form biofilms and hinder wound healing. In this study, S. epidermidis distribution in VLUs and associated resistome were analysed in ulcer tissue from patients. Virulence of S. epidermidis isolates from VLUs were evaluated by whole genome sequencing, antimicrobial susceptibility testing, in vitro biofilm and binding assays, and assessment of biofilm‐forming capability and pro‐inflammatory potential using human ex vivo wound model. We demonstrated that S. epidermidis isolates from VLUs inhibit re‐epithelialization through biofilm‐dependent induction of IL‐1β, IL‐8, and IL‐6 which was in accordance with impaired healing outcomes observed in patients. High extracellular matrix binding ability of VLU isolates was associated with antimicrobial resistance and expression levels of the embp and sdrG, responsible for bacterial binding to fibrinogen and fibrin, respectively. 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subjects Anti-Bacterial Agents - pharmacology
Biofilms - drug effects
Chronic Disease
Drug Resistance, Multiple, Bacterial
Female
Humans
infection
keratinocytes
Male
Microbial Sensitivity Tests
Original ‐basic Science
Staphylococcal Infections - microbiology
Staphylococcus epidermidis
translational research
Varicose Ulcer - microbiology
venous leg ulcer
wound healing
Wound Healing - drug effects
Wound Infection - drug therapy
Wound Infection - microbiology
title Multi‐drug resistant Staphylococcus epidermidis from chronic wounds impair healing in human wound model
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