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Clonal relatedness and conserved integron structures in epidemiologically unrelated Pseudomonas aeruginosa strains producing the VIM-1 metallo-{beta}-lactamase from different Italian hospitals.

RICCIO M. L.
•
PALLECCHI L.
•
DOCQUIER J. D.
altro
ROSSOLINI G. M.
2005
  • journal article

Periodico
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Abstract
Three epidemiologically independent Pseudomonas aeruginosa isolates, representative of the first VIM-1 metallo--lactamase producers detected at three different hospitals in northern Italy, were investigated to determine their genomic relatedness and to compare the structures of the genetic supports for the VIM-1 determinants. The three isolates, all of serotype O11, appeared to be clonally related according to the results of genotyping by macrorestriction analysis of genomic DNA by pulsed-field gel electrophoresis and random amplification of polymorphic DNA. Investigation of the genetic support for the blaVIM-1 determinant revealed that it was carried on identical or almost identical integrons (named In70.2 and In70.3) located within a conserved genomic context. The integrons were structurally related to In70 and In110, two plasmid-borne blaVIM-1-containing integrons from Achromobacter xylosoxidans and Pseudomonas putida isolates, respectively, from the same geographic area (northern Italy) and were found to be inserted close to the res site of a Tn5051-like transposon, different from any of those described previously, that was apparently carried on the bacterial chromosome. The present findings suggest that the three VIM-1-producing isolates are members of the same clonal complex which have been spreading in hospitals in northern Italy since the late 1990s and point to a common ancestry of their blaVIM-1-containing integrons.
DOI
10.1128/AAC.49.1.104–110.2005
Archivio
http://hdl.handle.net/11368/1695838
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-19944427459
Diritti
metadata only access
Soggetti
  • Pseudomonas aeruginos...

  • integron

  • metallo-beta-lactamas...

Scopus© citazioni
59
Data di acquisizione
Jun 7, 2022
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Data di acquisizione
Apr 19, 2024
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