β-Lactamase Producing Escherichia coli Encoding bla CTX-M and bla CMY Genes in Chicken Carcasses from Egypt.
Elham Elsayed Abo-AlmagdRana Fahmi SabalaSamir Mohammed Abd-ElghanyCharlene R JacksonHazem RamadanKálmán ImreAdriana MorarViorel HermanKhalid Ibrahim SallamPublished in: Foods (Basel, Switzerland) (2023)
Escherichia coli with multidrug resistance and β-lactamase genes may constitute a great public health hazard due to the potential for their transmission to humans through the food chain. This study determined the prevalence, antibiotic resistance profiles, phylogroups, and β-lactamase genes of E. coli isolates from chicken carcasses marketed in Mansoura, Egypt. Interestingly, E. coli was detected in 98% (98/100) of the chicken carcasses examined, which seemed among the highest contamination rates by E. coli worldwide. From the 425 genetically verified uidA gene-positive E . coli , 85 isolates were further studied for antimicrobial resistance profiles, phylogroups, and β-lactamase genes. Interestingly, 89.41% of E. coli (76/85) strains tested against 24 different antibiotics were multidrug-resistant. Of the examined 85 E. coli isolates, 22 (25.88%) isolates harbored bla CTX-M and were resistant to ampicillin, cefazoline, and ceftriaxone, while three of them were resistant to ceftazidime besides. Nine (10.59%) E. coli strains harbored AmpC- β-lactamase bla CMY and were resistant to ampicillin. One isolate co-carried bla CMY and bla CTX-M genes, though it was negative for the bla TEM gene. Of the 35 isolates that harbored either extended-spectrum β-lactamase (ESBL) and/or AmpC β-lactamase genes, six strains (17.14%) were assigned to pathogenic phylogroup F and one to phylogroup E, whereas 28 (80%) isolates belonged to commensal phylogenetic groups.
Keyphrases
- escherichia coli
- klebsiella pneumoniae
- genome wide
- genome wide identification
- multidrug resistant
- public health
- biofilm formation
- bioinformatics analysis
- genome wide analysis
- antimicrobial resistance
- genetic diversity
- dna methylation
- risk assessment
- transcription factor
- gram negative
- copy number
- risk factors
- gene expression
- human health
- climate change
- health risk
- global health