Sphingosine is able to prevent and eliminate Staphylococcus epidermidis biofilm formation on different orthopedic implant materials in vitro.


Journal

Journal of molecular medicine (Berlin, Germany)
ISSN: 1432-1440
Titre abrégé: J Mol Med (Berl)
Pays: Germany
ID NLM: 9504370

Informations de publication

Date de publication:
02 2020
Historique:
received: 07 08 2019
accepted: 18 11 2019
revised: 11 11 2019
pubmed: 22 12 2019
medline: 30 4 2021
entrez: 22 12 2019
Statut: ppublish

Résumé

Periprosthetic infection (PPI) is a devastating complication in joint replacement surgery. On the background of an aging population, the number of joint replacements and associated complications is expected to increase. The capability for biofilm formation and the increasing resistance of different microbes to antibiotics have complicated the treatment of PPI, requiring the need for the development of alternative treatment options. The bactericidal effect of the naturally occurring amino alcohol sphingosine has already been reported. In our study, we demonstrate the antimicrobial efficacy of sphingosine on three different strains of biofilm producing Staphylococcus epidermidis, representing one of the most frequent microbes involved in PPI. In an in vitro analysis, sphingosine's capability for prevention and treatment of biofilm-contamination on different common orthopedic implant surfaces was tested. Coating titanium implant samples with sphingosine not only prevented implant contamination but also revealed a significant reduction of biofilm formation on the implant surfaces by 99.942%. When testing the antimicrobial efficacy of sphingosine on sessile biofilm-grown Staphylococcus epidermidis, sphingosine solution was capable to eliminate 99.999% of the bacteria on the different implant surfaces, i.e., titanium, steel, and polymethylmethacrylate. This study provides evidence on the antimicrobial efficacy of sphingosine for both planktonic and sessile biofilm-grown Staphylococcus epidermidis on contaminated orthopedic implants. Sphingosine may provide an effective and cheap treatment option for prevention and reduction of infections in joint replacement surgery. KEY MESSAGES: • Here we established a novel technology for prevention of implant colonization by sphingosine-coating of orthopedic implant materials. • Sphingosine-coating of orthopedic implants prevented bacterial colonization and significantly reduced biofilm formation on implant surfaces by 99.942%. • Moreover, sphingosine solution was capable to eliminate 99.999% of sessile biofilm-grown Staphylococcus epidermidis on different orthopedic implant surfaces.

Identifiants

pubmed: 31863153
doi: 10.1007/s00109-019-01858-x
pii: 10.1007/s00109-019-01858-x
pmc: PMC7007894
doi:

Substances chimiques

Anti-Bacterial Agents 0
Polymethacrylic Acids 0
Steel 12597-69-2
polymethacrylic acid 25087-26-7
Titanium D1JT611TNE
Sphingosine NGZ37HRE42

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

209-219

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : Gu 335/34-1
Pays : International

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Auteurs

Sascha Beck (S)

Department of Molecular Biology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122, Essen, Germany. sascha.beck@uk-essen.de.
Department of Orthopedics and Orthopedic Surgery, Saarland University Medical Center and Saarland University Faculty of Medicine, Homburg, Germany. sascha.beck@uk-essen.de.

Carolin Sehl (C)

Department of Molecular Biology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122, Essen, Germany.

Sylvia Voortmann (S)

Institute for Experimental Immunology and Imaging, Medical Research Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Hedda Luise Verhasselt (HL)

Institute of Medical Microbiology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Michael J Edwards (MJ)

Department of Surgery, University of Cincinnati, Cincinnati, USA.

Jan Buer (J)

Institute of Medical Microbiology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Mike Hasenberg (M)

Institute for Experimental Immunology and Imaging, Medical Research Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Erich Gulbins (E)

Department of Molecular Biology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122, Essen, Germany.
Department of Surgery, University of Cincinnati, Cincinnati, USA.

Katrin Anne Becker (KA)

Department of Molecular Biology, Medical School Essen, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122, Essen, Germany. katrin.anne.becker@uni-due.de.

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Classifications MeSH