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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 1
2007 pubmed

Sensitivity of Chlamydia suis to cathelicidin peptides.

Donati. Manuela M; Di Francesco. Antonietta A; Gennaro. Renato R; Benincasa. Monica M; Magnino. Simone S; Pignanelli. Salvatore S; Shurdhi. Alisa A; Moroni. Alessandra A; Mazzoni. Claudio C; Merialdi. Giuseppe G; Baldelli. Raffaella R; Cevenini. Roberto R

Key Findings

  • SMAP‑29 reduced Chlamydia inclusion numbers at 10 µg/ml in most isolates
  • Some isolates were resistant even at 80 µg/ml
  • LL‑37 and PG‑1 showed no anti‑chlamydial effect at 80 µg/ml

Practical Outcomes

  • LL‑37 isn’t effective against this Chlamydia strain, so it isn’t a viable antimicrobial supplement for this purpose. The results suggest focusing on other peptides if targeting similar bacteria, but the findings have limited direct relevance to human health or typical biohacking protocols.

Summary

The study tested several natural antimicrobial peptides, including LL‑37, against a pig‑related Chlamydia infection. LL‑37 didn’t work even at high doses, while another peptide (SMAP‑29) showed some activity. For most biohackers, this doesn’t give a useful new health hack.

Abstract

Nine Chlamydia suis isolates, obtained from pigs with conjunctivitis, were molecularly characterized by ompA sequencing and their in vitro susceptibility to six cathelicidin peptides (SMAP-29, BAC-7, BMAP-27, BMAP-27, BMAP-28, PG-1, LL-37) determined in cell culture. SMAP-29 was the most active peptide, reducing the intracellular inclusion number by > or =50% at a concentration of 10 microg/ml (3 microM) in six of the nine isolates tested. Three molecularly identical isolates were insensitive at a concentration as high as 80 microg/ml (25 microM). Of the remaining cathelicidin peptides tested, BAC-7 and BMAP-27 were active against six C. suis isolates at a concentration of 80 microg/ml (25 and 26 microM, respectively). Cathelicidins LL-37 and PG-1 did not show any anti-chlamydial activity at 80 microg/ml.

Study Information

Provider

pubmed

Year

2007

Date

2007-02-16T00:00:00.000Z

DOI

10.1016/j.vetmic.2007.02.011