| Literature DB >> 31006638 |
Lindsay R Kalan1, Jacquelyn S Meisel2, Michael A Loesche3, Joseph Horwinski3, Ioana Soaita3, Xiaoxuan Chen3, Aayushi Uberoi3, Sue E Gardner4, Elizabeth A Grice5.
Abstract
Chronic wounds are a major complication of diabetes associated with high morbidity and health care expenditures. To investigate the role of colonizing microbiota in diabetic wound healing, clinical outcomes, and response to interventions, we conducted a longitudinal, prospective study of patients with neuropathic diabetic foot ulcers (DFU). Metagenomic shotgun sequencing revealed that strain-level variation of Staphylococcus aureus and genetic signatures of biofilm formation were associated with poor outcomes. Cultured wound isolates of S. aureus elicited differential phenotypes in mouse models that corresponded with patient outcomes, while wound "bystanders" such as Corynebacterium striatum and Alcaligenes faecalis, typically considered commensals or contaminants, also significantly impacted wound severity and healing. Antibiotic resistance genes were widespread, and debridement, rather than antibiotic treatment, significantly shifted the DFU microbiota in patients with more favorable outcomes. These findings suggest that the DFU microbiota may be a marker for clinical outcomes and response to therapeutic interventions.Entities:
Keywords: antibiotic resistance; chronic wounds; diabetes; metagenomics; microbiome; wound healing
Mesh:
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Year: 2019 PMID: 31006638 PMCID: PMC6526540 DOI: 10.1016/j.chom.2019.03.006
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023