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Identification, Synthesis, and In Vitro Activities of Antimicrobial Peptide from African Catfish against the Extended-Spectrum Beta-Lactamase (ESBL)-Producing Escherichia coli.
Okella, Hedmon; Odongo, Steven; Vertommen, Didier; Okello, Emmanuel.
Affiliation
  • Okella H; Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, CA 93274, USA.
  • Odongo S; Department of Biotechnical and Diagnostic Sciences, College of Veterinary Medicine, Animal Resources and Biosecurity, Makerere University, Kampala P.O. Box 7062, Uganda.
  • Vertommen D; de Duve Institute and MASSPROT Platform, UCLouvain, 1200 Brussels, Belgium.
  • Okello E; Veterinary Medicine Teaching and Research Center, School of Veterinary Medicine, University of California, Davis, CA 93274, USA.
Pharmaceutics ; 16(7)2024 Jun 22.
Article de En | MEDLINE | ID: mdl-39065546
ABSTRACT
The global surge in multi-drug resistant bacteria, including extended-spectrum ß-lactamase (ESBL)-producing Escherichia coli has led to a growing need for new antibacterial compounds. Despite being promising, the potential of fish-derived antimicrobial peptides (AMPs) in combating ESBL-producing E. coli is largely unexplored. In this study, native African catfish antimicrobial peptides (NACAPs) were extracted from the skin mucus of farmed African catfish, Clarias gariepinus, using a combination of 10% acetic acid solvent hydrolysis, 5 kDa ultrafiltration, and C18 hydrophobic interaction chromatography. Peptides were then sequenced using Orbitrap Fusion Lumos Tribrid Mass Spectrometry. The identified peptides were screened for potential antibacterial activity using Random Forest and AdaBoost machine learning algorithms. The most promising peptide was chemically synthesized and evaluated in vitro for safety on rabbit red blood cells and activity against ESBL-producing E. coli (ATCC 35218) utilizing spot-on-lawn and broth dilution methods. Eight peptides ranging from 13 to 22 amino acids with molecular weights between 968.42 and 2434.11 Da were identified. Peptide NACAP-II was non-hemolytic to rabbit erythrocytes (p > 0.05) with a zone of inhibition (ZOI) of 22.7 ± 0.9 mm and a minimum inhibitory concentration (MIC) of 91.3 ± 1.2 µg/mL. The peptide is thus a candidate antibacterial compound with enormous potential applications in the pharmaceutical industry. However, further studies are still required to establish an upscale production strategy and optimize its activity and safety in vivo.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pharmaceutics Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pharmaceutics Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique