Nicola C Osborne, Rosa Catania, Snow Stolnik, Karen Robinson
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The liposomes were characterized for αLA and amoxicillin content, particle size, membrane fluidity and permeability, prior to their addition to cultures of <i>H. pylori</i> strains and clinical isolates. αLA-modified liposomes enhanced the antibacterial action of amoxicillin against <i>H. pylori</i>, as determined using a viable count method. The liposomal formulation achieved a 3-log reduction in bacterial density, compared to a 1.5- to 2-log reduction by amoxicillin in solution. The application of imaging cytometry revealed a significantly increased association of αLA-modified liposomes with <i>H. pylori</i> cells, compared to non-αLA control liposomes. In conclusion, this study demonstrated, for the first time, that the incorporation of αLA increased the attraction of the liposomes to <i>H. pylori</i> and increased antibiotic potency. This suggests that αLA incorporation into liposomes may not only act as an antimicrobial, but also as a potential <i>in vivo</i> targeting strategy.</p>","PeriodicalId":49819,"journal":{"name":"Microbiology-Sgm","volume":"171 5","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12125478/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>Alpha</i>-linolenic acid-modified liposomes associate with and modulate antibiotic activity against <i>Helicobacter pylori</i>.\",\"authors\":\"Nicola C Osborne, Rosa Catania, Snow Stolnik, Karen Robinson\",\"doi\":\"10.1099/mic.0.001562\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fatty acids have antimicrobial activity against a wide range of bacteria. 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The liposomal formulation achieved a 3-log reduction in bacterial density, compared to a 1.5- to 2-log reduction by amoxicillin in solution. The application of imaging cytometry revealed a significantly increased association of αLA-modified liposomes with <i>H. pylori</i> cells, compared to non-αLA control liposomes. In conclusion, this study demonstrated, for the first time, that the incorporation of αLA increased the attraction of the liposomes to <i>H. pylori</i> and increased antibiotic potency. 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Alpha-linolenic acid-modified liposomes associate with and modulate antibiotic activity against Helicobacter pylori.
Fatty acids have antimicrobial activity against a wide range of bacteria. We therefore aimed to incorporate omega-3 unsaturated alpha-linolenic acid (αLA) into the membrane of antibiotic-loaded liposomes to create a system with dual antibacterial activity against Helicobacter pylori. Liposomes containing 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine, cholesterol, sphingomyelin and the far-red fluorescent DiD label, with varying content of αLA (mol% to total lipid), were fabricated using the thin film evaporation method and hydrated with PBS or amoxicillin solution. The liposomes were characterized for αLA and amoxicillin content, particle size, membrane fluidity and permeability, prior to their addition to cultures of H. pylori strains and clinical isolates. αLA-modified liposomes enhanced the antibacterial action of amoxicillin against H. pylori, as determined using a viable count method. The liposomal formulation achieved a 3-log reduction in bacterial density, compared to a 1.5- to 2-log reduction by amoxicillin in solution. The application of imaging cytometry revealed a significantly increased association of αLA-modified liposomes with H. pylori cells, compared to non-αLA control liposomes. In conclusion, this study demonstrated, for the first time, that the incorporation of αLA increased the attraction of the liposomes to H. pylori and increased antibiotic potency. This suggests that αLA incorporation into liposomes may not only act as an antimicrobial, but also as a potential in vivo targeting strategy.
期刊介绍:
We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms.
Topics include but are not limited to:
Antimicrobials and antimicrobial resistance
Bacteriology and parasitology
Biochemistry and biophysics
Biofilms and biological systems
Biotechnology and bioremediation
Cell biology and signalling
Chemical biology
Cross-disciplinary work
Ecology and environmental microbiology
Food microbiology
Genetics
Host–microbe interactions
Microbial methods and techniques
Microscopy and imaging
Omics, including genomics, proteomics and metabolomics
Physiology and metabolism
Systems biology and synthetic biology
The microbiome.