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Genomic Characterization of MDR Escherichia coli Harboring blaOXA-48 on the IncL/M-type Plasmid Isolated from Blood
S Alousi1, T Salloum1, H Arabaghian1
1Department of Natural Sciences, School of Arts & Sciences, Lebanese American University, Byblos, Lebanon.
Abstract:
Escherichia coli is responsible for a wide variety of community and hospital acquired extraintestinal infections, and the emergence of ESBL resistant isolates is a major clinical concern. In this study, we characterized the genomic attributes of an OXA-48 and CTX-M-3 producing E. coli EC-IMP153. Whole-genome initial assembly produced 146 contigs with a combined 5,504,170 bp in size and a G+C content of 50.5%. wgSNPs-based phylogenetic comparison with 36 publically available genomes was also performed. Comprehensive genomic analysis showed that EC-IMP153 belonged to sequence type ST-405 and harbored several resistance determinants including the β-lactam resistance genes blaOXA-48, blaCTX-M-3, blaTEM-1B, blaOXA-1, and blaCMY-70, aminoglycoside fyuA and aac(3)IId, tetracycline tet(A) and tet(R), and fluoroquinolone gyrA, parC, and mfd resistance determinants. Plasmids with the following incompatibility groups were detected in silico and confirmed using PBRT: IncI1-α, IncL, IncW, Col (BS512), and IncF. To our knowledge this is the first in-depth genomic analysis of an OXA-48 producing E. coli ST-405 isolated from a patient in Lebanon and linked to a blood stream infection. Continuous monitoring is necessary to better understand the continued diffusion of such pathogens, especially in view of the population movements triggered by unrest in the Middle East.
Insights
This study details the genomic analysis of an OXA-48 and CTX-M-3 producing Escherichia coli strain (EC-IMP153) from Lebanon. The findings highlight its multidrug resistance and ST-405 lineage, crucial for understanding pathogen spread.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Extraintestinal pathogenic Escherichia coli (E. coli) infections are a significant public health concern.
- The rise of multidrug-resistant (MDR) E. coli, particularly those producing extended-spectrum beta-lactamases (ESBLs), poses a major clinical challenge.
- OXA-48 and CTX-M-3 are critical carbapenemase and ESBL enzymes, respectively, conferring resistance to important antibiotics.
Purpose of the Study:
- To perform a comprehensive genomic characterization of an OXA-48 and CTX-M-3 co-producing E. coli isolate (EC-IMP153).
- To identify the genetic basis of antibiotic resistance and understand the phylogenetic context of the isolate.
- To provide insights into the emergence and dissemination of MDR E. coli in Lebanon.
Main Methods:
- Whole-genome sequencing (WGS) and initial assembly to determine genome size and contig number.
- Phylogenetic analysis using whole-genome single nucleotide polymorphisms (wgSNPs) compared to public E. coli genomes.
- In silico and experimental plasmid analysis to identify resistance gene-carrying plasmids.
Main Results:
- The E. coli isolate EC-IMP153 genome consisted of 146 contigs (5,504,170 bp, 50.5% G+C content).
- EC-IMP153 belongs to Sequence Type 405 (ST-405) and carries multiple resistance genes (blaOXA-48, blaCTX-M-3, blaTEM-1B, blaOXA-1, blaCMY-70, fyuA, aac(3)IId, tet(A), tet(R), gyrA, parC, mfd).
- Multiple plasmid incompatibility groups (IncI1-α, IncL, IncW, Col(BS512), IncF) were detected, carrying resistance determinants.
Conclusions:
- This is the first in-depth genomic analysis of an OXA-48 producing E. coli ST-405 from a bloodstream infection in Lebanon.
- The isolate possesses a significant MDR profile, including ESBL and carbapenemase genes, posing a threat to patient treatment.
- Continuous genomic surveillance is essential to track the spread of such MDR pathogens, especially considering regional population movements.
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