New endogenous antimicrobial peptides (AMPs) derived from chromogranin A (CgA) are secreted by nervous, endocrine and
immune cells during stress. They display antimicrobial activities by lytic effects at micromolar range using a pore-forming mechanism
against Gram-positive bacteria, filamentous fungi and yeasts. These AMPs can also penetrate quickly into neutrophils (without lytic
effects), where, similarly to “cell penetrating peptides”, they interact with cytoplasmic calmodulin, and induce calcium influx via Store
Operated Channels therefore triggering neutrophils activation. Staphylococcus aureus and Salmonella enteritis are bacteria responsible
for severe infections. We investigated here the effects of S. aureus and S. enteritis bacterial proteases on CgA-derived peptides and
evaluated their antimicrobial activities. We showed that the Glu-C protease produced by S. aureus V8 induces the loss of the AMPs
antibacterial activities and produces new antifungal peptides. In addition, four antimicrobial CGA-derived peptides (chromofungin, procatestatin,
human/bovine catestatin) are degraded when treated with bacterial supernatants from S. aureus and S. enteritis, whereas,
cateslytin, the short active form of catestatin, resists to this degradation. Finally, we demonstrate that several antimicrobial CgA-derived
peptides are able to act synergistically with antibiotics against bacteria and fungi indicating their roles in innate defense.
Keywords: Innate immunity, antimicrobial peptides, antibiotics, chromogranins, catestatin, chromofungin, Staphylococcus aureus,
Salmonella enteritis, neutrophils, bacterial proteases, synergy, neuroendocrine system, immune system.
Rights & PermissionsPrintExport