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. 2009 Sep 22;64(6):1170–1174. doi: 10.1093/jac/dkp341

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© The Author 2009. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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(a) Genetic organization of transposons Tn6001, Tn6001.1 and Tn6001.2 in P. aeruginosa isolates. Genes are shown as arrows, with their orientation of transcription indicated by the arrowheads. A4, aacA4 gene. The sizes and location of the multiplex PCR amplicons are displayed in Tn6001. IRi, left-hand integron inverted repeat (25 bp); IRt, right-hand integron inverted repeat (25 bp); TIRL: left-hand transposon inverted repeat; f-TIRR: potential right-hand transposon inverted repeat. (b) Three different bla_VIM-2-harbouring integron cassettes were amplified by two primer sets.