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Updated: Aug 5, 2026

Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression
Published on: April 18, 2025
Ranalexin-1G: A Promising Antimicrobial Peptide Targeting Virulence and Host-Pathogen Interactions in Pseudomonas
Marina Acunzo1, Carla Zannella1,2, Rosa Giugliano1
1Department of Woman, Child and General and Specialized Surgery, University of Campania Luigi Vanvitelli, 80138 Naples, Italy.
Background:
Lung infections represent a major cause of morbidity and mortality in patients with cystic fibrosis (CF) and are predominantly associated with chronic infection by Pseudomonas aeruginosa. The clinical management of CF lung disease is increasingly compromised by the emergence of multidrug-resistant strains, biofilm formation, and the expression of multiple virulence determinants. Antimicrobial peptides (AMPs), evolutionarily conserved effectors of innate immunity, have emerged as promising therapeutic candidates due to their ability to exert both bactericidal and anti-virulence activities. In this study, we investigated the antimicrobial and mechanistic effects of Ranalexin-1G, an AMP derived from the skin secretion of Rana grylio, against P. aeruginosa, for which its antibacterial activity has not previously been reported in the literature.
Methods:
Antibacterial activity was determined against the reference strain and three clinical isolates of P. aeruginosa by broth microdilution assays, time-kill kinetics and anti-biofilm assays, while peptide-mediated modulation of virulence was evaluated through transcriptional analysis of key virulence-associated genes by RT-PCR. The impact of Ranalexin-1G on host-pathogen interactions was further assessed using bacterial invasion assays in human bronchial epithelial cells (BEAS-2B).
Results:
Ranalexin-1G exerted a rapid bactericidal effect within 6 h at non-cytotoxic concentrations and displayed modest anti-biofilm effects, with greater efficacy in inhibiting biofilm formation. Mechanistically, peptide treatment resulted in a reduction in the expression of selected genes involved in biofilm formation and virulence, including those associated with alginate biosynthesis and type III secretion system-mediated cytotoxicity. Consistently, Ranalexin-1G markedly impaired bacterial invasion of epithelial cells, indicating interference with early host-pathogen interaction processes. Notably, the peptide displayed robust antimicrobial activity against multidrug-resistant P. aeruginosa clinical isolates from CF patients.
Conclusions:
Collectively, these findings suggest that Ranalexin-1G acts through a dual mechanism involving direct bactericidal activity and modulation of selected virulence pathways, supporting further investigation of its potential as an anti-virulence and host-directed approach for the treatment of chronic P. aeruginosa infections in cystic fibrosis.
Insights
Ranalexin-1G, a novel antimicrobial peptide, effectively kills multidrug-resistant Pseudomonas aeruginosa and inhibits its virulence. This peptide shows promise for treating chronic P. aeruginosa infections in cystic fibrosis patients.
Area of Science:
- Microbiology
- Infectious Diseases
- Peptide Therapeutics
Background:
- Lung infections are a major cause of mortality in cystic fibrosis (CF) patients, often due to chronic Pseudomonas aeruginosa infections.
- Multidrug-resistant strains, biofilm formation, and virulence factors complicate CF lung disease management.
- Antimicrobial peptides (AMPs) are promising therapeutic candidates due to their bactericidal and anti-virulence properties.
Purpose of the Study:
- To investigate the antimicrobial and mechanistic effects of Ranalexin-1G, an AMP from Rana grylio skin secretions, against Pseudomonas aeruginosa.
- To evaluate Ranalexin-1G's efficacy against multidrug-resistant P. aeruginosa strains from CF patients.
Main Methods:
- Antibacterial activity assessed via broth microdilution, time-kill kinetics, and anti-biofilm assays.
- Virulence gene expression analyzed using RT-PCR.
- Impact on host-pathogen interactions evaluated through bacterial invasion assays in human bronchial epithelial cells (BEAS-2B).
Main Results:
- Ranalexin-1G demonstrated rapid bactericidal effects at non-cytotoxic concentrations within 6 hours.
- The peptide showed modest anti-biofilm activity, with greater efficacy in inhibiting biofilm formation.
- Ranalexin-1G reduced the expression of virulence-associated genes and impaired bacterial invasion of epithelial cells.
- Effective antimicrobial activity was observed against multidrug-resistant P. aeruginosa clinical isolates from CF patients.
Conclusions:
- Ranalexin-1G exhibits a dual mechanism of action: direct bactericidal activity and modulation of virulence pathways.
- These findings support Ranalexin-1G's potential as an anti-virulence and host-directed therapy for chronic P. aeruginosa infections in CF.
- Further investigation is warranted for Ranalexin-1G's therapeutic application in cystic fibrosis.
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