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Published online ahead of print on 15 June 2009 as doi:10.1099/jmm.0.010017-0
Journal of Medical Microbiology 2009;58:1080.

J Med Microbiol (2009), DOI: 10.1099/jmm.0.010017-0
© 2009 Society for General Microbiology
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Relevance of resistance levels to carbapenems and integron-borne blaIMP-1, blaIMP-7, blaIMP-10 and blaVIM-2 in clinical isolates of Pseudomonas aeruginosa

Wei-Hua Zhao1, Gelin Chen, Ribu Ito and Zhi-Qing Hu

Showa University School of Medicine

1 E-mail: whzhao{at}med.showa-u.ac.jp

Received February 4, 2009
Accepted April 15, 2009

The molecular detection and surveillance of the resistant genes harbored by Pseudomonas aeruginosa become more and more important, to assess and control their spread and colonization in hospitals, and to guide treatment of the infections. In this study, we analyzed the resistance mechanisms of carbapenem-resistant clinical isolates of P. aeruginosa and identified the associated integron-borne metallo-β-lactamase (MBL) genes. Twenty-seven imipenem-resistant clinical isolates of P. aeruginosa were divided into three groups according to their resistance levels to carbapenems. Strains bearing blaIMP-10 showed extremely high level resistance to imipenem with MICs of 512 to 2048 µg ml-1. By comparison, strains bearing the blaIMP-1, blaIMP-7 and blaVIM-2 showed the middle level of resistance with MICs of 32 to 256 µg ml-1. The non-MBL-producing strains showed low level of resistance with MICs of 8 to 32 µg ml-1. The same trend in resistance levels was also observed when resistance to other carbapenems such as meropenem and panipenem were determined. DNA sequencing showed that the MBL gene cassettes were carried by class 1 integrons. The blaIMP-1, blaIMP-7 and blaIMP-10 gene cassettes were preceded by a hybrid Pant promoter, TGGACA-N17-TAAACT, and the blaVIM-2 gene cassette was preceded by a weak Pant promoter, TGGACA-N17-TAAGCT. Most of the MBL genes were linked with one or two resistance genes encoding aminoglycoside-modifying enzymes, such as aac(6')Iae, aac(6')II, aacA7, aacC4, aadA1, aadA2 and aadA6, highlighting the multidrug-resistant properties of these clinical isolates.







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