Genomic and biological characterization of bacteriophages against Enterobacter cloacae, a high-priority pathogen
Enterobacter cloacae is a clinically significant pathogen due to its multi-resistance to antibiotics, presenting a challenge in the treatment of infections. As concerns over antibiotic resistance escalate, novel therapeutic approaches have been explored. Bacteriophages, characterized by their remark...
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Veröffentlicht in: | Virology (New York, N.Y.) N.Y.), 2024-07, Vol.595, p.110100-110100, Article 110100 |
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Sprache: | eng |
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Zusammenfassung: | Enterobacter cloacae is a clinically significant pathogen due to its multi-resistance to antibiotics, presenting a challenge in the treatment of infections. As concerns over antibiotic resistance escalate, novel therapeutic approaches have been explored. Bacteriophages, characterized by their remarkable specificity and ability to self-replicate within target bacteria, are emerging as a promising alternative therapy. In this study, we isolated and partially characterized nine lytic bacteriophages targeting E. cloacae, with two selected for comprehensive genomic analysis based on their host range and bacteriolytic activity. All identified phages exhibited a narrow host range, demonstrated stability within a temperature range of 30–60 °C, displayed pH tolerance from 3 to 10, and showed an excellent bacteriolytic capacity for up to 18 h. Notably, the fully characterized phage genomes revealed an absence of lysogenic, virulence, or antibiotic-resistance genes, positioning them as promising candidates for therapeutic intervention against E. cloacae-related diseases. Nonetheless, translating this knowledge into practical therapeutic applications mandates a deeper understanding of bacteriophage interactions within complex biological environments.
•Lytic bacteriophages exhibit host-specific activity against E. cloacae.•The phages exhibited efficient bacteriolytic activity for up to 18 h at 0.1 MOI.•Thorough characterization reveals the absence of undesirable genes in phage genomes. |
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ISSN: | 0042-6822 1096-0341 |
DOI: | 10.1016/j.virol.2024.110100 |