Multiresistant Pseudomonas aeruginosa serogroup Ο:11 outbreak in an intensive care unit |
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Authors: | Panayotis T. Tassios Vassiliki Gennimata Lemonia Spaliara-Kalogeropoulou Dimitris Kairis Chryssa Koutsia Alkiviadis C. Vatopoulos Nicholas J. Legakis |
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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 |
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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. |
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Keywords: | Pseudomonas aeruginosa nosocomial infection antibiotic resistance serotyping bacteriocin typing pulsed-field gel electrophoresis |
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