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. 2012 Oct;50(10):3202-7.
doi: 10.1128/JCM.01423-12. Epub 2012 Jul 18.

High metabolic potential may contribute to the success of ST131 uropathogenic Escherichia coli

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High metabolic potential may contribute to the success of ST131 uropathogenic Escherichia coli

Tarek M Gibreel et al. J Clin Microbiol. 2012 Oct.

Abstract

Uropathogenic Escherichia coli (UPEC) is the predominant cause of urinary tract infection in both hospital and community settings. The recent emergence of multidrug-resistant clones like the O25b:H4-ST131 lineage represents a significant threat to health, and numerous studies have explored the virulence potential of these organisms. Members of the ST131 clone have been described as having variable carriage of key virulence factors, and it has been suggested that additional unidentified factors contribute to virulence. Here we demonstrated that ST131 isolates have high metabolic potential and biochemical profiles that distinguish them from isolates of many other sequence types (STs). A collection of 300 UPEC isolates recovered in 2007 and 2009 in the Northwest region of England were subjected to metabolic profiling using the Vitek2 Advanced Expert System (AES). Of the 47 tests carried out, 30 gave a positive result with at least one of the 300 isolates examined. ST131 isolates demonstrated significant association with eight tests, including those for peptidase, decarboxylase, and alkalinization activity. Metabolic activity also correlated with antibiotic susceptibility profiles, with resistant organisms displaying the highest metabolic potential. This is the first comprehensive study of metabolic potential in the ST131 lineage, and we suggest that high metabolic potential may have contributed to the fitness of members of the ST131 clone, which are able to exploit the available nutrients in both the intestinal and urinary tract environments.

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Figures

Fig 1
Fig 1
UPGMA cluster analysis based on the biochemical profiles of major sequence types.
Fig 2
Fig 2
Biotype profiling of ST131 isolates: cluster analysis based on metabolic profiles.
Fig 3
Fig 3
Distribution of metabolic profiles of UPEC isolates. ST131 isolates displayed at the left side of the x axis (left of the black line crossing the x axis) were predominantly susceptible, and those on the right side were resistant (as projected earlier by cluster analysis).

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