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Background and objectives:
The aim of the study was to analyse the genetic environment of plasmid-borne blaCTX-M-1 genes ofEscherichia coli isolates from diseased food-producing animals.
Materials and methods:
The ESBL gene blaCTX-M-1 was identified in 352 of 7,810 E. coli isolates from diseased food-producing animals collected in GERM-Vet (2008-2015).Fifty representative isolates were subjected to plasmid transfer experiments and whole genome sequencing. The transformed plasmids were characterized by PCR-based replicon typing and PCR assays for the detection of co-located resistance genes.
Results:
The plasmids were positive for nine different replicons or replicon combinations, one plasmid was non-typeable. ISEcp1, bracketed by 5-bp direct repeats,was associated with blaCTX-M-1 on most IncI1 plasmids. On IncN, IncFII and most IncF plasmids ISEcp1 was truncated by IS26 in the upstream region and downstream a Δmrx-mph(A) cluster was detected followed by IS26at varying positions in the sequences of different plasmids. Commonly detected co-located antimicrobial resistance genes conferred resistance to sulphonamides, aminoglycosides and tetracycline.
Conclusions:
The genetic environment of the blaCTX-M-1 genes was diverse, but similarities among the different plasmid families were noted. IncN, IncI1 and IncF plasmids play a role in the dissemination of blaCTX-M-1;the co-located antimicrobial resistance genes may facilitate the spread and persistence of this ESBL gene.