Extended spectrum beta-lactamases in Escherichia coli from municipal wastewater

Tatiana Čornejová 1, Jan Venglovsky 1, Gabriela Gregova 1, Marta Kmetova 2, Vladimir Kmet 3
1 - University of Veterinary Medicine and Pharmacy, Košice, Slovakia
2 - Faculty of Medicine, Department of Medical Microbiology and Clinical Microbiology, P. J. Safarik University, Kosice, Slovakia
3 - Institute of Animal Physiology, Slovak Academy of Sciences, Košice, Slovakia
Ann Agric Environ Med
2015; 22 (3):
ICID: 1167710
Article type: Original article
 
 
Introduction and objective. Over the past decades, awareness of the environmental load of resistant organisms has increased. The presented paper focuses on antibiotic resistance and detection of resistance genes in environmental E. coli and on the evaluation of biofilm formation in ESBLs (extended spectrum beta-lactamase) producing E. coli isolated from an urban wastewater treatment plant.
Materials and method. Wastewater samples and artificially added polystyrene pellets were used as the source for E. coli isolation. Minimal inhibitory concentrations of 19 antibiotics were determined according to CLSI (2013). Biofilm formation was investigated by crystal violet or resazurin methods. CTX-M, carbapenemases, qnrS, mobile elements and virulence factors were determined by PCR. Clonal relatedness of strains was detected by principal component analysis by a Maldi biotyper.
Results. ESBL phenotype was detected in 26% of environmental strains. CTX-M, CMY-2 and qnrS genes of antibiotic resistance were detected. IMP gene together with integron 1 in one ertapenem resistant E. coli was also recorded. There was no evident correlation between antibiotic resistance, virulence and biofilm production.
Conclusions. The results showed that the wastewater is a source of ESBLs, carbapenemases and plasmid fluoroquinolone resistance. Strains with biofilm production, antibiotic resistance of CTX-M group, CMY-2, qnrS genes and virulence factors present a potential environmental health risk.
DOI: 10.5604/12321966.1167710
PMID 26403112 - click here to show this article in PubMed
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