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    Streptokinase reduces Streptococcus dysgalactiae subsp. equisimilis biofilm formation (2024)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Tölken, Lea A.
    Neufend, Janine V.
    Oppegaard, Oddvar
    Methling, Karen
    Moll, Kirsten
    Redanz, Sylvio
    Katsburg, Miriam M. D. (WE 7)
    Ali, Murtadha Q.
    Shumba, Patience
    Kreikemeyer, Bernd
    Skrede, Steinar
    Fulde, Marcus (WE 7)
    Norrby-Teglund, Anna
    Lalk, Michael
    Kittang, Bård R.
    Siemens, Nikolai
    Quelle
    BMC microbiology
    Bandzählung: 24
    Heftzählung: 1
    Seiten: 378
    ISSN: 1471-2180
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://bmcmicrobiol.biomedcentral.com/articles/10.1186/s12866-024-03540-w
    DOI: 10.1186/s12866-024-03540-w
    Pubmed: 39350011
    Kontakt
    Institut für Mikrobiologie und Tierseuchen

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51843 / 66949
    mikrobiologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    Background: Streptococcus dysgalactiae subspecies equisimilis (SDSE) is increasingly recognized as an emerging cause of invasive diseases including necrotizing soft tissue infections (NSTIs). In contrast to the closely related Streptococcus pyogenes, SDSE infections mainly affect older and comorbid patients. Biofilm formation has been demonstrated in soft tissue biopsies of S. pyogenes NSTI cases.

    Results: Here, we show that bacterial aggregations indicative of biofilms are also present in SDSE NSTI. Although streptokinase (Ska) activity and biofilm formation did not correlate in a diverse set of clinical SDSE isolates, addition of exogenous Ska at an early time point prevented biofilm formation for selected strains. Deletion of ska in SDSE S118 strain resulted in increased biofilm forming capacity. Ska-deficient mutant strain was characterized by a higher metabolic activity and consequent metabolome profiling of biofilms identified higher deposition of a wide range of metabolites as compared to the wild-type.

    Conclusions: Our results argue that Ska suppresses biofilm formation in SDSE independent of its original plasminogen converting activity. However, the impact of biofilms and its consequences for patient outcomes in streptococcal NSTIs remain to be elucidated.