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Acinetobacter baumannii Global Clone-Specific Resistomes Explored in Clinical Isolates Recovered from Egypt
Samira M Hamed1, Walid F Elkhatib2,3, Hanka Brangsch4
1Department of Microbiology and Immunology, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), Giza 12451, Egypt.
Antibiotics (Basel, Switzerland)
|July 29, 2023
Summary
This study analyzed 46 Acinetobacter baumannii clinical isolates, revealing extensive antibiotic resistance. The carbapenem resistance gene blaOXA-23 was prevalent across all global clone lineages in Egyptian isolates.
Area of Science:
- Medical Microbiology
- Genomic Epidemiology
- Antimicrobial Resistance
Background:
- Acinetobacter baumannii is a critical opportunistic pathogen known for rapid acquisition of antibiotic resistance.
- Understanding the genomic basis of drug resistance in clinical isolates is crucial for effective treatment strategies.
Purpose of the Study:
- To investigate the genomic epidemiology and characterize the resistome of multidrug-resistant Acinetobacter baumannii clinical isolates.
- To identify key resistance genes and genetic elements contributing to antimicrobial resistance in specific global clone lineages.
Main Methods:
- Whole-genome sequencing of 46 Acinetobacter baumannii clinical isolates.
- Antimicrobial susceptibility testing using broth microdilution.
- In silico multi-locus sequence typing and resistome analysis.
Main Results:
- High rates of multi-, extensive-, and pan-drug resistance were observed, with limited susceptibility to colistin, amikacin, and trimethoprim/sulfamethoxazole.
- The blaOXA-23 carbapenem resistance gene was the most prevalent, found in 69.6% of isolates across all identified global clones.
- Novel sequence types were identified, and specific resistance genes like blaOXA-23 and sul1 were distributed across all global clones.
Conclusions:
- The study highlights the significant contribution of five global clones to Acinetobacter baumannii infections in Egypt.
- Comprehensive analysis revealed GC-specific resistomes and the widespread dissemination of blaOXA-23, emphasizing the urgent need for antimicrobial stewardship.

