In vitro bactericidal and bacteriolytic activity of ceragenin CSA-13 against planktonic cultures and biofilms of Streptococcus pneumoniae and other pathogenic streptococci.

PLoS One

Centro de Investigaciones Biológicas, CSIC, Madrid, Spain; CIBER de Enfermedades Respiratorias (CIBERES), Mallorca, Illes Balears, Spain.

Published: March 2015

Ceragenin CSA-13, a cationic steroid, is here reported to show a concentration-dependent bactericidal/bacteriolytic activity against pathogenic streptococci, including multidrug-resistant Streptococcus pneumoniae. The autolysis promoted by CSA-13 in pneumococcal cultures appears to be due to the triggering of the major S. pneumoniae autolysin LytA, an N-acetylmuramoyl-L-alanine amidase. CSA-13 also disintegrated pneumococcal biofilms in a very efficient manner, although at concentrations slightly higher than those required for bactericidal activity on planktonic bacteria. CSA-13 has little hemolytic activity which should allow testing its antibacterial efficacy in animal models.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090064PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0101037PLOS

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Article Synopsis
  • Ceragenins (CSAs) are promising new antimicrobials that imitate natural antimicrobial peptides found in the body, showing effectiveness against a major cause of hospital infections.* -
  • In experiments, CSAs CSA-13, CSA-44, and CSA-131 demonstrated strong bactericidal effects on various clinical isolates, even disrupting biofilms that protect bacteria on surfaces.* -
  • CSA-13 was particularly effective in preventing bacteria from sticking to lung epithelial cells, indicating its potential role in hindering bacterial infections and suggesting further development for therapeutic use.*
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Ceragenin-mediated disruption of Pseudomonas aeruginosa biofilms.

PLoS One

February 2024

Department of Medical Microbiology and Nanobiomedical Engineering, Medical University of Białystok, Białystok, Poland.

Background: Microbial biofilms, as a hallmark of cystic fibrosis (CF) lung disease and other chronic infections, remain a desirable target for antimicrobial therapy. These biopolymer-based viscoelastic structures protect pathogenic organisms from immune responses and antibiotics. Consequently, treatments directed at disrupting biofilms represent a promising strategy for combating biofilm-associated infections.

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Ceragenins, including CSA-13, are cationic antimicrobials that target the bacterial cell envelope differently than colistin. However, the molecular basis of their action is not fully understood. Here, we examined the genomic and transcriptome responses by Enterobacter hormaechei after prolonged exposure to either CSA-13 or colistin.

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Ceragenin CSA-13 displays high antibacterial efficiency in a mouse model of urinary tract infection.

Sci Rep

November 2022

Department of Medical Microbiology and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2C, 15-222, Białystok, Poland.

Ceragenins (CSAs) are synthetic, lipid-based molecules that display activities of natural antimicrobial peptides. Previous studies demonstrated their high in vitro activity against pathogens causing urinary tract infections (UTIs), but their efficiency in vivo was not explored to date. In this study, we aimed to investigate the bactericidal efficiency of ceragenins against E.

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Background: Stenotrophomonas maltophilia is a Gram-negative bacterium resistant to several antibiotics and its prevalence in cystic fibrosis (CF) patients is increasing.

Objectives: To evaluate the effects of ceragenins, non-peptide mimics of antimicrobial peptides, against both planktonic and biofilm forms of S. maltophilia and the cytotoxicity of ceragenins to the IB3-1 CF cell line.

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