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Rigshospitalet - a part of Copenhagen University Hospital
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Integrated univariate, multivariate and correlation-based network analyses reveal metabolite-specific effects on bacterial growth and biofilm formation in necrotizing soft tissue infections

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  1. Quantitative proteome profiling of normal human circulating microparticles

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  2. Long-term patient-important outcomes after septic shock: a protocol for 1-year follow-up of the CLASSIC-trial

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  3. Periocular necrotizing soft tissue infection in Greater Copenhagen

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Necrotizing soft-tissue infections (NSTIs) have multiple causes, risk factors, anatomical locations, and pathogenic mechanisms. In patients with NSTI, circulating metabolites may serve as a substrate having impact on bacterial adaptation at the site of infection. Metabolic signatures associated with NSTI may reveal the potential to be useful as diagnostic and prognostic markers and novel targets for therapy. This study used untargeted metabolomics analyses of plasma from NSTI patients (n = 34) and healthy (noninfected) controls (n = 24) to identify the metabolic signatures and connectivity patterns among metabolites associated with NSTI. Metabolite-metabolite association networks were employed to compare the metabolic profiles of NSTI patients and noninfected surgical controls. Out of 97 metabolites detected, the abundance of 33 was significantly altered in NSTI patients. Analysis of metabolite-metabolite association networks showed a more densely connected network: Specifically, 20 metabolites differentially connected between NSTI and controls. A selected set of significantly altered metabolites was tested in vitro to investigate potential influence on NSTI group A streptococcal strain growth and biofilm formation. Using chemically defined media supplemented with the selected metabolites, ornithine, ribose, urea, and glucuronic acid, revealed metabolite-specific effects on both bacterial growth and biofilm formation. This study identifies for the first time an NSTI-specific metabolic signature with implications for optimized diagnostics and therapies.

Original languageEnglish
JournalJournal of Proteome Research
Volume19
Issue number2
Pages (from-to)688-698
Number of pages11
ISSN1535-3893
DOIs
Publication statusPublished - 7 Feb 2020

    Research areas

  • bacterial infection, differential network analysis, metabolomics, necrotizing fasciitis, necrotizing soft-tissue infections, streptococcus

ID: 58863173