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Antibiotic-chemoattractants enhance neutrophil clearance of Staphylococcus aureus.
- Source :
-
Nature communications [Nat Commun] 2021 Oct 25; Vol. 12 (1), pp. 6157. Date of Electronic Publication: 2021 Oct 25. - Publication Year :
- 2021
-
Abstract
- The pathogen Staphylococcus aureus can readily develop antibiotic resistance and evade the human immune system, which is associated with reduced levels of neutrophil recruitment. Here, we present a class of antibacterial peptides with potential to act both as antibiotics and as neutrophil chemoattractants. The compounds, which we term 'antibiotic-chemoattractants', consist of a formylated peptide (known to act as chemoattractant for neutrophil recruitment) that is covalently linked to the antibiotic vancomycin (known to bind to the bacterial cell wall). We use a combination of in vitro assays, cellular assays, infection-on-a-chip and in vivo mouse models to show that the compounds improve the recruitment, engulfment and killing of S. aureus by neutrophils. Furthermore, optimizing the formyl peptide sequence can enhance neutrophil activity through differential activation of formyl peptide receptors. Thus, we propose antibiotic-chemoattractants as an alternate approach for antibiotic development.<br /> (© 2021. The Author(s).)
- Subjects :
- Amino Acid Sequence
Animals
Anti-Bacterial Agents chemistry
Anti-Bacterial Agents therapeutic use
Bacterial Load drug effects
Chemotactic Factors chemistry
Chemotactic Factors therapeutic use
Drug Resistance, Bacterial drug effects
Immunotherapy
Mice
Neutrophils immunology
Neutrophils metabolism
Peptides chemistry
Peptides pharmacology
Phagocytosis drug effects
Receptors, Formyl Peptide metabolism
Staphylococcal Infections immunology
Staphylococcal Infections microbiology
Staphylococcal Infections therapy
Vancomycin chemistry
Vancomycin pharmacology
Anti-Bacterial Agents pharmacology
Chemotactic Factors pharmacology
Neutrophils drug effects
Staphylococcus aureus drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 34697316
- Full Text :
- https://doi.org/10.1038/s41467-021-26244-5