Bactericidal Activity to Escherichia coli : Different Modes of Action of Two 24-Mer Peptides SAAP-148 and OP-145, Both Derived from Human Cathelicidine LL-37

• Published in: Antibiotics (Basel) Vol. 12; no. 7; p. 1163
• Main Authors: Ön, Ayse, Vejzovic, Djenana, Jennings, James, Parigger, Lena, Cordfunke, Robert A, Drijfhout, Jan Wouter, Lohner, Karl, Malanovic, Nermina
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 08.07.2023; MDPI
• Subjects: Antigens; Antiinfectives and antibacterials; Antimicrobial activity; Antimicrobial agents; Antimicrobial peptides; Bacteria; Bactericidal activity; Calorimetry; Cardiolipin; Cytoplasmic membranes; Depolarization; Differential scanning calorimetry; E coli; Escherichia coli; Genotype & phenotype; Gram-negative bacteria; Gram-positive bacteria; Lipids; lipid–peptide interaction; Lipopolysaccharides; LPS; membrane permeabilization; Membrane potential; Membranes; Mode of action; Peptides; Permeability; Phenotypes; Phosphatidylethanolamine; Phosphatidylglycerol; Zeta potential; lipid–peptide interaction; LPS; membrane permeabilization
• ISSN: 2079-6382; 2079-6382
• DOI: 10.3390/antibiotics12071163

OP-145 and SAAP-148, two 24-mer antimicrobial peptides derived from human cathelicidin LL-37, exhibit killing efficacy against both Gram-positive and Gram-negative bacteria at comparable peptide concentrations. However, when it comes to the killing activity against , the extent of membrane permeabilization does not align with the observed bactericidal activity. This is the case in living bacteria as well as in model membranes mimicking the cytoplasmic membrane (CM). In order to understand the killing activity of both peptides on a molecular basis, here we studied their mode of action, employing a combination of microbiological and biophysical techniques including differential scanning calorimetry (DSC), zeta potential measurements, and spectroscopic analyses. Various membrane dyes were utilized to monitor the impact of the peptides on bacterial and model membranes. Our findings unveiled distinct binding patterns of the peptides to the bacterial surface and differential permeabilization of the CM, depending on the smooth or rough/deep-rough lipopolysaccharide (LPS) phenotypes of strains. Interestingly, the antimicrobial activity and membrane depolarization were not significantly different in the different LPS phenotypes investigated, suggesting a general mechanism that is independent of LPS. Although the peptides exhibited limited permeabilization of membranes, DSC studies conducted on a mixture of synthetic phosphatidylglycerol/phosphatidylethanolamine/cardiolipin, which mimics the CM of Gram-negative bacteria, clearly demonstrated disruption of lipid chain packing. From these experiments, we conclude that depolarization of the CM and alterations in lipid packing plays a crucial role in the peptides' bactericidal activity.