Evidence map›Paper›PMID 39350011›Full record

ArticleBMC microbiology2024

Streptokinase reduces Streptococcus dysgalactiae subsp. equisimilis biofilm formation.

Lea A Tölken, Janine V Neufend, Oddvar Oppegaard, Karen Methling, Kirsten Moll, Sylvio Redanz, Miriam M D Katsburg, Murtadha Q Ali, Patience Shumba, Bernd Kreikemeyer and 6 more

Abstract read
In one paragraph

Article in BMC microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. High-throughput chip-calorimeter using a BiMicrosystems & nanoengineering · 2025
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Lea A Tölken *Department of Molecular Genetics and Infection Biology, University of Greifswald, Greifswald, Germany.
Janine V Neufend *Department of Molecular Genetics and Infection Biology, University of Greifswald, Greifswald, Germany.
Oddvar OppegaardDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Karen MethlingDepartment of Cellular Biochemistry and Metabolomics, Institute of Biochemistry, University of Greifswald, Greifswald, Germany.
Kirsten MollCenter for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
Sylvio RedanzDepartment of Translational Rheumatology and Immunology, Institute of Musculoskeletal Medicine, University of Münster, Münster, Germany.
Miriam M D KatsburgCenter for Infection Medicine, Institute of Microbiology and Epizootics, Freie Universität Berlin, Berlin, Germany.
Murtadha Q AliDepartment of Molecular Genetics and Infection Biology, University of Greifswald, Greifswald, Germany.
Patience ShumbaDepartment of Molecular Genetics and Infection Biology, University of Greifswald, Greifswald, Germany.
Bernd KreikemeyerInstitute for Microbiology, Virology and Hygiene, University Medicine Rostock, Rostock, Germany.
Steinar SkredeDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Marcus FuldeCenter for Infection Medicine, Institute of Microbiology and Epizootics, Freie Universität Berlin, Berlin, Germany.
Anna Norrby-TeglundCenter for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden.
Michael LalkDepartment of Cellular Biochemistry and Metabolomics, Institute of Biochemistry, University of Greifswald, Greifswald, Germany.
Bård R KittangDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Nikolai SiemensDepartment of Molecular Genetics and Infection Biology, University of Greifswald, Greifswald, Germany. nikolai.siemens@uni-greifswald.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStreptococcus 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.

resultsHere, 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.

conclusionsOur 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.

Indexed as

BiofilmsStreptococcal InfectionsStreptococcusStreptokinaseBacterial ProteinsHumansSoft Tissue InfectionsBacterial ProteinsStreptokinaseBiofilmNecrotizing soft tissue infectionsStreptococcus dysgalactiae subsp. equisimilisStreptokinase

Identifiers

PMID39350011
PMCPMC11440690

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.