Chronic wound microenvironment mediates selection of biofilm-forming multi drug resistant Staphylococcus epidermidis with capability to impair healing.
Irena PastarMiroslav DinicRebecca VerpileJingjing MengJelena MarjanovicJamie BurgessLisa PlanoSuzanne HowerSeth ThallerSantanu BanerjeeHadar Lev-TovMarjana Tomic-CanicPublished in: Research square (2023)
Venous leg ulcers (VLU) are the most common chronic wounds characterized by bacterial biofilms and perturbed microbiome. Staphylococcus epidermidis is primarily known as skin commensal beneficial for the host, however, some strains can form biofilms and cause infections. By employing shotgun metagenomic sequencing we show that genetic signatures of antimicrobial resistance, adhesion and biofilm formation in VLU isolates correlate with in vitro bacterial traits. We demonstrate that the capability of chronic wound isolates to form biofilms and elicit IL-8 and IL-1β expression in human ex vivo wounds, correlates with the non-healing outcomes in patients with VLU. In contrast, commensal strains were incapable of surviving in the human ex vivo wounds. We show that major fitness traits of S. epidermis from VLU involve genes for resistance to methicillin and mupirocin, while the biofilm formation relied on the minimal number of genetic elements responsible for bacterial binding to fibronectin and fibrinogen. This underscores the importance of the emergence of treatment resistant virulent lineages in patients with non-healing wounds.
Keyphrases
- biofilm formation
- candida albicans
- staphylococcus aureus
- genome wide
- drug resistant
- escherichia coli
- wound healing
- pseudomonas aeruginosa
- antimicrobial resistance
- endothelial cells
- acinetobacter baumannii
- multidrug resistant
- poor prognosis
- dna methylation
- induced pluripotent stem cells
- cystic fibrosis
- copy number
- body composition
- stem cells
- physical activity
- methicillin resistant staphylococcus aureus
- single cell
- skeletal muscle
- pluripotent stem cells
- microbial community
- long non coding rna
- genome wide identification
- binding protein
- insulin resistance
- anaerobic digestion
- type iii