First Report and Characterization of a Plasmid-Encoded bla SFO-1 in a Multi-Drug-Resistant Aeromonas hydrophila Clinical Isolate.
Troy SkworDan Christopher JonesCaitlin CahakRyan J NewtonPublished in: Microorganisms (2024)
Antibiotic resistance remains one of the most pressing public health issues facing the world today. At the forefront of this battle lies the ever-increasing identification of extended-spectrum beta-lactamases and carbapenemases within human pathogens, conferring resistance towards broad-spectrum and last-resort antimicrobials. This study was prompted due to the identification of a pathogenic Aeromonas hydrophila isolate (strain MAH-4) collected from abdominal fluid, which presented a robust resistance pattern against second-, third-, and fourth-generation cephalosporins, ertapenem, ciprofloxacin, gentamicin, levofloxacin and moxifloxacin, and beta lactam/beta-lactamase inhibitor combinations. Whole genome sequencing was performed and identified a 328 kb plasmid (pMAH4) encoding 10 antibiotic resistance genes, including bla SFO-1 , bla TEM-1 , and bla OXA-1 of A. hydrophia MAH-4. This is the first report of beta-lactamase SFO-1 within a clinical strain of Aeromonas . Due to the remarkable sequence identity of pMAH4 to plasmids associated with Enterobacterales genera like Klebsiella and the extensive capabilities of Aeromonas for horizontal gene transfer, our identification of a clinical isolate encoding SFO-1 on a plasmid suggests antibiotic resistance gene mobility between Enterobacterales and non- Enterobacterales species.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- multidrug resistant
- drug resistant
- gram negative
- public health
- acinetobacter baumannii
- antibiotic resistance genes
- crispr cas
- endothelial cells
- genome wide
- copy number
- pseudomonas aeruginosa
- bioinformatics analysis
- wastewater treatment
- transcription factor
- genome wide identification