Skip Navigation


JAC Advance Access originally published online on July 1, 2006
Journal of Antimicrobial Chemotherapy 2006 58(3):530-536; doi:10.1093/jac/dkl266
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
58/3/530    most recent
dkl266v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (8)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Yan, J.-J.
Right arrow Articles by Wu, J.-J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yan, J.-J.
Right arrow Articles by Wu, J.-J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Characterization of acquired ß-lactamases and their genetic support in multidrug-resistant Pseudomonas aeruginosa isolates in Taiwan: the prevalence of unusual integrons

Jing-Jou Yan1, Po-Ren Hsueh4, Jang-Jih Lu5, Feng-Yee Chang6, Wen-Chien Ko2 and Jiunn-Jong Wu3,*

1 Departments of Pathology, College of Medicine, National Cheng Kung University No. 1 University Road, Tainan 70101, Taiwan 2 Internal Medicine, College of Medicine, National Cheng Kung University No. 1 University Road, Tainan 70101, Taiwan 3 Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University No. 1 University Road, Tainan 70101, Taiwan 4 Department of Laboratory Medicine, National Taiwan University Hospital No.7 Chung San South Road, Taipei 10002, Taiwan 5 Departments of Pathology, Tri-service General Hospital Sec. 2, 325 Chenggong Road, Taipei 11490, Taiwan 6 Internal Medicine, Tri-service General Hospital Sec. 2, 325 Chenggong Road, Taipei 11490, Taiwan

Received 10 March 2006; returned 2 May 2006; revised 19 May 2006; accepted 1 June 2006


*Corresponding author. Tel: +886-6-2353535 ext. 5605; Fax: +886-6-2363956; E-mail: jjwu{at}mail.ncku.edu.tw

Objectives: The present study was conducted to investigate acquired ß-lactamases and their genetic support in 26 Pseudomonas aeruginosa isolates that were resistant to nearly all antipseudomonal drugs from six medical centres in Taiwan.

Methods: Acquired ß-lactamases and their genetic support were determined by PCR-based strategies.

Results: Four and 16 of the 26 isolates were found to produce VIM-2 and VIM-3 metallo-ß-lactamases (MBLs), respectively, and 1, 1 and 2 isolates produced OXA-17, OXA-10 and PSE-1, respectively. These bla genes are all in class 1 integrons that are probably chromosomally located. The blaVIM-3-containing integron, with a deletion between int1 and the blaVIM-3 structural gene, has six gene cassettes, blaVIM-3, a probable fosfomycin resistance determinant, aacA4, aacA4, aadB and aacA4. The blaVIM-2-containing integron, without detectable 5'-conserved segment, contains four genes cassettes (aacA7-blaVIM-2-dhfr-aacA5) and is ended by tniC. The blaOXA-10-containing integron includes a catB3 cassette and a fused gene cassette, which is made up of blaOXA-17 and a novel streptomycin–spectinomycin gene, designated aadA15. The blaOXA-17-containing integron has three gene cassettes (aacA4-catB2-blaOXA-17) but the 59-base element of the blaOXA-17 cassette is interrupted by a putative transposase gene. The blaPSE-1-containing integron has three gene cassettes, aacA4, an aadA3-related gene designated aadA3b and blaPSE-1. PFGE revealed genetic diversity among the multidrug-resistant isolates from different hospitals.

Conclusions: This study demonstrated the high prevalence of VIM-type MBLs and the presence of unusual bla-encoding integrons in multidrug-resistant P. aeruginosa isolates in Taiwan. The spread of blaVIM-2-related genes by horizontal transfer might have occurred.

Keywords: carbapenemases , penicillinases , gene cassettes , fosfomycin


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Antimicrob. Agents Chemother.Home page
O. Samuelsen, L. Buaro, M. A. Toleman, C. G. Giske, N. O. Hermansen, T. R. Walsh, and A. Sundsfjord
The First Metallo-{beta}-Lactamase Identified in Norway Is Associated with a TniC-Like Transposon in a Pseudomonas aeruginosa Isolate of Sequence Type 233 Imported from Ghana
Antimicrob. Agents Chemother., January 1, 2009; 53(1): 331 - 332.
[Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
S.-P. Tseng, P.-R. Hsueh, J.-C. Tsai, and L.-J. Teng
Tn6001, a Transposon-Like Element Containing the blaVIM-3-Harboring Integron In450
Antimicrob. Agents Chemother., November 1, 2007; 51(11): 4187 - 4190.
[Abstract] [Full Text] [PDF]


Home page
Clin. Microbiol. Rev.Home page
A. M. Queenan and K. Bush
Carbapenemases: the Versatile {beta}-Lactamases
Clin. Microbiol. Rev., July 1, 2007; 20(3): 440 - 458.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
J.-J. Wu, W.-C. Ko, S.-H. Tsai, and J.-J. Yan
Prevalence of Plasmid-Mediated Quinolone Resistance Determinants QnrA, QnrB, and QnrS among Clinical Isolates of Enterobacter cloacae in a Taiwanese Hospital
Antimicrob. Agents Chemother., April 1, 2007; 51(4): 1223 - 1227.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.