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Multiresistant Pseudomonas aeruginosa serogroup Ο:11 outbreak in an intensive care unit
Authors:Panayotis T. Tassios  Vassiliki Gennimata  Lemonia Spaliara-Kalogeropoulou  Dimitris Kairis  Chryssa Koutsia  Alkiviadis C. Vatopoulos  Nicholas J. Legakis
Affiliation:Department of Microbiology, Medical School, University of Athens, Athens, Greece;Microbiology Laboratory, Voula General Hospital, Athens, Greece;Department of Hygiene and Epidemiology, Medical School, University of Athens, Athens, Greece
Abstract:Objective: To determine whether 15 multiresistant Pseudomonas aeruginosa isolates from an intensive care unit (ICU) outbreak were related, were endemic, and belonged to the Ο:12 European clone.
Methods: Forty-six P. aeruginosa isolates from a large hospital were investigated with respect to their antibiotic resistance profiles, serogroups, bacteriocin types and DNA fingerprints obtained by pulsed-field gel electrophoresis (PFGE) of genomic DNA digested with Xba l.
Results: Fourteen of the ICU outbreak isolates were indeed identical with respect to their serogroup, Ο:11, pyocin type, 10/a, and PFGE type, A. Clone A was endemic and dominant throughout the hospital, even though, within the ICU, it underwent phenotypic alterations, such as loss of cell wall lipopolysaccharide side-chains, or acquisition of ceftazidime and imipenem resistance. Bacteriocin typing was more discriminatory than serotyping, but PFGE could differentiate further among phenotypically identical strains. It also allowed the tracking of an Ο:6 strain, as it was becoming gradually more resistant and undergoing a bacteriocin-type conversion while remaining genotypically unaltered.
Conclusions: Using three typing methods, a nosocomial multiresistant strain distinct from the previously described dominant European Ο:12 clone was characterized, and the ability of PFGE to identify clonal isolates even when these appear phenotypically distinct was demonstrated.
Keywords:Pseudomonas aeruginosa    nosocomial infection    antibiotic resistance    serotyping    bacteriocin typing    pulsed-field gel electrophoresis
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