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. 2011 Aug;49(8):2905-10.
doi: 10.1128/JCM.00753-11. Epub 2011 Jun 22.

Wide dispersion of ST175 clone despite high genetic diversity of carbapenem-nonsusceptible Pseudomonas aeruginosa clinical strains in 16 Spanish hospitals

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Wide dispersion of ST175 clone despite high genetic diversity of carbapenem-nonsusceptible Pseudomonas aeruginosa clinical strains in 16 Spanish hospitals

María García-Castillo et al. J Clin Microbiol. 2011 Aug.

Abstract

During the COMParative Activity of Carbapenems Testing (COMPACT) surveillance study, 448 Pseudomonas aeruginosa clinical isolates were obtained from 16 Spanish hospitals. Nonsusceptibility (EUCAST breakpoints) to imipenem (35%), meropenem (33%), and/or doripenem (33%) was observed with 175 isolates (39%). Simultaneous resistance to these three drugs was observed with 126 of the 175 isolates (72%). Except for colistin, high resistance rates were observed among noncarbapenem antibiotics. Clonal relatedness was investigated by pulsed-field gel electrophoresis (PFGE) with SpeI, discriminating 68 patterns. Multilocus sequence typing (MLST) was performed on 84 isolates representing different PFGE types and all participating hospitals. Thirty-nine sequence types (STs) could be distinguished, and of these, ST175 (48 isolates, 10 hospitals), ST646 (16 isolates, 4 hospitals), ST532 (13 isolates, 3 hospitals), and ST111 (13 isolates, 7 hospitals) were the most frequently encountered. Minimum-spanning tree analysis confirmed a wide dissemination of different clones among participant hospitals, particularly ST175. PFGE pattern comparison within the four most frequent STs revealed that ST175 isolates were relatively uniform, while ST646, ST532, and ST111 isolates were highly diverse, with almost every isolate belonging to a unique pulsotype, even when originating from the same center. The population of carbapenem-nonsusceptible P. aeruginosa isolates from 16 hospitals is highly diverse, with one ST (ST175) representing a highly conserved clone disseminated in 10 of the 16 participant hospitals. This ST175 clone should be added to the list of P. aeruginosa clones at high risk for epidemic spread, such as the Liverpool, Manchester, and Melbourne clones previously found in cystic fibrosis patients and ST235 in the nosocomial setting.

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Figures

Fig. 1.
Fig. 1.
MIC distribution of 175 clinical P. aeruginosa isolates for each carbapenem studied that were not susceptible to at least imipenem (MIC, >4 μg/ml), meropenem (MIC, >2 μg/ml), or doripenem (MIC, > 1 μg/ml).
Fig. 2.
Fig. 2.
Minimum-spanning tree of 175 P. aeruginosa clinical isolates. Each color represents a single hospital (n = 16). Wide lines represent single-locus variants, dotted lines represent multilocus variants, and the size of the circles represents the number of isolates found with the respective ST.
Fig. 3.
Fig. 3.
PFGE-SpeI of the different pulsotypes detected for ST175 (A) and ST646 (B) in isolates from different hospitals.

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