Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2022 pubmed 32 citations

Coating and Corruption of Human Neutrophils by Bacterial Outer Membrane Vesicles.

du Teil Espina. Marines M; Fu. Yanyan Y; van der Horst. Demi D; Hirschfeld. Claudia C; López-Álvarez. Marina M; Mulder. Lianne M LM; Gscheider. Costanza C; Haider Rubio. Anna A; Huitema. Minke M; Becher. Dörte D; Heeringa. Peter P; van Dijl. Jan Maarten JM

Key Findings

  • P. gingivalis outer membrane vesicles (OMVs) coat and activate neutrophils without killing them
  • Neutrophil‑released antimicrobial peptides LL‑37 and myeloperoxidase are degraded by OMV‑bound gingipain proteases
  • Degradation of LL‑37 helps the bacteria survive and promotes chronic inflammation, a pattern also seen with another oral pathogen

Practical Outcomes

  • Keep your mouth clean and consider therapies that target gingipain enzymes to protect LL‑37’s antimicrobial action. Reducing periodontal infection may help maintain innate immunity and lower systemic inflammation linked to diseases like arthritis or Alzheimer’s.

Summary

The study shows that a gum‑disease bacterium, Porphyromonas gingivalis, releases tiny vesicles that stick to your immune cells (neutrophils) and make them release antimicrobial peptides like LL‑37, but the bacteria’s enzymes then chew up LL‑37, letting the bugs survive and keep inflammation going. This helps explain why gum disease can link to other health problems.

Abstract

Porphyromonas gingivalis is a keystone oral pathogen that successfully manipulates the human innate immune defenses, resulting in a chronic proinflammatory state of periodontal tissues and beyond. Here, we demonstrate that secreted outer membrane vesicles (OMVs) are deployed by P. gingivalis to selectively coat and activate human neutrophils, thereby provoking degranulation without neutrophil killing. Secreted granule components with antibacterial activity, especially LL-37 and myeloperoxidase (MPO), are subsequently degraded by potent OMV-bound proteases known as gingipains, thereby ensuring bacterial survival. In contrast to neutrophils, the P. gingivalis OMVs are efficiently internalized by macrophages and epithelial cells. Importantly, we show that neutrophil coating is a conserved feature displayed by OMVs of at least one other oral pathogen, namely, Aggregatibacter actinomycetemcomitans. We conclude that P. gingivalis deploys its OMVs for a neutrophil-deceptive strategy to create a favorable inflammatory niche and escape killing. <b>IMPORTANCE</b> Severe periodontitis is a dysbiotic inflammatory disease that affects about 15% of the adult population, making it one of the most prevalent diseases worldwide. Importantly, periodontitis has been associated with the development of nonoral diseases, such as rheumatoid arthritis, pancreatic cancer, and Alzheimer's disease. Periodontal pathogens implicated in periodontitis can survive in the oral cavity only by avoiding the insults of neutrophils while at the same time promoting an inflamed environment where they successfully thrive. Our present findings show that outer membrane vesicles secreted by the keystone pathogen Porphyromonas gingivalis provide an effective delivery tool of virulence factors that protect the bacterium from being killed while simultaneously activating human neutrophils.

Study Information

Provider

pubmed

Year

2022

Date

2022-08-24T00:00:00.000Z

DOI

10.1128/spectrum.00753-22

Citations

32

References

67