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    Characterization of blaCTX-M-1 gene regions on plasmids from Escherichia coliisolates collected in the GERM-Vet resistance monitoring program 2008-2015 fromdiseased food-producing animals (2019)

    Art
    Poster
    Autoren
    Schink, A.-K. (WE 7)
    Michael, G. B.
    Hanke, D. (WE 7)
    Kaspar, H.
    Falgenhauer, L.
    Imirzalioglu, C.
    Chakraborty, T.
    Schwarz, S. (WE 7)
    Kongress
    Zoonoses 2019 - International Symposium on Zoonoses Research
    Berlin, 16. – 18.10.2019
    Quelle
    Zoonoses 2019 - International Symposium on Zoonoses Research : Book of Abstracts — International Symposium on Zoonoses Research (Hrsg.)
    Berlin, 2019 — S. 242
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://evis.events/event/79/attachments/23/154/Book_of_Abstracts_Zoonoses2019.pdf
    Kontakt
    Institut für Mikrobiologie und Tierseuchen

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51843 / 66949
    mikrobiologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    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.