Sphingosine kills intracellular Pseudomonas aeruginosa and Staphylococcus aureus.

Pseudomonas aeruginosa Staphyloccus aureus Sphingosine ceramide cystic fibrosis sphingolipids

Journal

Pathogens and disease
ISSN: 2049-632X
Titre abrégé: Pathog Dis
Pays: United States
ID NLM: 101595366

Informations de publication

Date de publication:
19 Jul 2024
Historique:
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: aheadofprint

Résumé

Sphingosine has been previously shown to kill many strains of pathogenic bacteria including Pseudomonas aeruginosa, Staphyloccus aureus, Acinetobacter and atypical mycobacteria. However, these studies were performed on isolated or extracellular bacteria and it is unknown whether sphingosine also targets intracellular bacteria. Here, we demonstrate that exogenously-added sphingosine directly binds to extracellular P. aeruginosa and S. aureus, but also targets and binds to intracellular bacteria. Intracellular sphingosine and bacteria were identified by sequential immunostainings. We further show that exogenously-added sphingosine also kills intracellular P. aeruginosa and S. aureus using modified gentamycin assays. Intracellular killing of P. aeruginosa and S. aureus by sphingosine is not mediated by improved phagosomal-lysosomal fusion. In summary, our data indicate that sphingosine binds to and most likely also directly kills extra- and intracellular P. aeruginosa and S. aureus.

Identifiants

pubmed: 39030066
pii: 7717365
doi: 10.1093/femspd/ftae016
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of FEMS.

Auteurs

Helene May (H)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Yongjie Liu (Y)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Stephanie Kadow (S)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Michael J Edwards (MJ)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Simone Keitsch (S)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Barbara Wilker (B)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Markus Kamler (M)

Department of Thoracic and Cardiovascular Surgery, Thoracic Transplantation, University Hospital Essen, University Duisburg-Essen, West German Heart and Vascular Center, Essen, Germany.

Heike Grassmé (H)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Yuqing Wu (Y)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Erich Gulbins (E)

Institute of Molecular Biology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Classifications MeSH