<i>Legionella pneumophila</i>-Induced NETs Do Not Bear LL-37 Peptides.
Iliadi. Valeria V; Marti. Stefania S; Skeva. Aikaterini A; Marmanis. Konstantinos K; Tsavdaridou. Theofani T; Euthymiou. Georgios G; Tryfonopoulou. Eleni E; Themelidis. Dimitrios D; Xanthopoulou. Athina A; Chlichlia. Katerina K; Koffa. Maria M; Konstantinidis. Theocharis T; Panopoulou. Maria M
Key Findings
- Legionella triggers NET formation without LL‑37, limiting antimicrobial effect
- IL‑1β is present on NETs during infection
- Clarithromycin treatment causes NETs to acquire LL‑37, which then inhibits bacterial proliferation
Practical Outcomes
- For biohackers, the main takeaway is that simply adding LL‑37 isn’t enough to fight Legionella; the antibiotic clarithromycin appears to enable LL‑37‑decorated NETs. However, using antibiotics as a health‑optimizing tool carries risks and isn’t a recommended longevity strategy. More research is needed before any LL‑37 supplementation or clarithromycin‑based protocol can be advised.
Summary
The study shows that during Legionella infection neutrophils release DNA traps (NETs) but these traps normally lack the antimicrobial peptide LL‑37, so they don’t stop the bacteria. When patients are treated with the antibiotic clarithromycin, the NETs do pick up LL‑37 and can suppress bacterial growth. This suggests the drug, not the peptide alone, changes how the immune traps work.
Abstract
<i>Legionella pneumophila</i> (<i>L. pneumophila</i>) infection is characterized by a wide spectrum of manifestations, from influenza-like illness to life-threatening atypical pneumonia with multiorgan failure. The aim of our study was the assessment of in vitro and ex vivo neutrophil activation in <i>L. pneumophila</i> infections, as well as the role of neutrophils' peptides such as LL-37 in infection. The ability of neutrophils to form ex vivo extracellular traps (NETs) in response to bacterial infection was examined by immunofluorescence. In parallel, patients' sera, as well as opsonized standard <i>L. pneumophila</i> strains, were used for in vitro activation of neutrophils from healthy individuals. The serum levels of interleukins were assessed using the LEGENDplexTM Multi-Analyte Flow Assay Kit. Furthermore, citrullinated cf-DNA as a marker of neutrophil extracellular traps (NETs) was detected in the serum of patients with acute infection. It was demonstrated that neutrophils released NETs in vitro and ex vivo upon <i>L. pneumophila</i> (interaction in an autophagy-independent manner. Notably, IL-1b was detected on NETs, but an antimicrobial peptide LL-37 was absent. The lack of antimicrobial activity failed to inhibit bacterial proliferation. In addition, in vitro and ex vivo NETs formation was observed during the Clarithromycin treatment. Those NETs were decorated with bioactive antimicrobial peptide LL-37, which inhibits bacterial proliferation. The findings provide evidence that neutrophils release NETs in vitro and ex vivo by expressing the IL1β protein in them. The lack of expression of the antimicrobial peptide LL-37 on the NETs demonstrates the inability of the cells to inhibit proliferation, and consequently the elimination of <i>L. pneumophila</i>. Clarithromycin plays a dual role in the elimination.
Study Information
pubmed
2025
2025-10-03T00:00:00.000Z
10.3390/microorganisms13102298
38