Human histone fragments display antibacterial properties against Pseudomonas aeruginosa.

Authors

Nourice Jaber, Angela Di Somma, Armando A Rodríguez Alfonso, Carolina Cané, Clarissa Read, Ludger Ständker, Sebastian Wiese, Angela Duilio, Jan Münch, Barbara Spellerberg

Published in

Frontiers in immunology. Volume 17. Pages 1879460. Epub Aug 12, 2026.

Abstract

Rising antimicrobial resistance rates require new therapeutic approaches such as antimicrobial peptides (AMPs), which are part of the innate immune defense, as alternatives to antibiotics. In this study, we aim to unravel the antibacterial activity of human histone H1.2 peptide against Pseudomonas aeruginosa and its potential immune modulatory role.
We used a hemofiltrate peptide database for antimicrobial peptide prediction to identify novel human AMPs. Thirteen sequences of histone H1 were identified as putative AMPs, synthesized, and tested against bacterial ESKAPE pathogens in a radial diffusion assay. SYTOX green assay, electrophoretic mobility shift assay, and differential proteomics assays were conducted to determine the mode of action of H1.2 peptide fragment. A crystal violet assay was performed to evaluate the inhibition of biofilm formation. The cytotoxicity of the peptide was tested in LDH and Alamar assays. Finally, to visualize the contributions of H1.2 in the formation of synthetic microwebs, scanning electron microscopy was performed.
The H1.2 peptide inhibited the growth of P. aeruginosa in a dose and pH-dependent manner without cytotoxicity towards mammalian THP-1 cells. It acts on intracellular targets to inhibit the growth of P. aeruginosa. STRING analysis from the differential proteomics assay showed that H1.2 targets the downregulation of proteins involved in the biogenesis of outer membrane proteins, including the folding and trafficking of outer membrane proteins across the cytoplasmic membrane. Scanning electron microscopy images showed that H1.2 forms microweb-like matrices capable of trapping and immobilizing P. aeruginosa.
The characterized antimicrobial activity of H1.2 points to a role for human histone H1 fragments in innate immunity and may represent a promising approach for the development of novel antibacterial therapies.

PMID:
42656251
Bibliographic data and abstract were imported from PubMed on 27 Aug 2026.

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