Skip Navigation


JAC Advance Access originally published online on November 16, 2007
Journal of Antimicrobial Chemotherapy 2008 61(1):219-220; doi:10.1093/jac/dkm444
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
61/1/219    most recent
dkm444v1
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 arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Walsh, F.
Right arrow Articles by Rogers, T. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Walsh, F.
Right arrow Articles by Rogers, T. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2007. 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

Research letters

Detection of blaVIM-2 carbapenemase in Pseudomonas aeruginosa in Ireland

F. Walsh* and T. R. Rogers

Department of Clinical Microbiology, Trinity College Dublin, St James's Hospital, Dublin 8, Ireland


* Corresponding author. Tel: +353-1-896-3620; E-mail: walshf1@tcd.ie

Keywords: P. aeruginosa , metallo-β-lactamases , MBLs

The first 10% of the full text of this article appears below.

Sir,

Pseudomonas aeruginosa is one of the most frequently isolated Gram-negative pathogens associated with hospital-acquired infections. The carbapenems, imipenem and meropenem, have a broad spectrum of activity and are considered the agents of choice for the treatment of P. aeruginosa infections. However, metallo-β-lactamases (MBLs), which readily hydrolyse most β-lactams, including carbapenems, are increasingly being identified among P. aeruginosa clinical isolates. The VIM-type MBLs have been widespread in Asia, Southern Europe and . . . [Full Text of this Article]


    Funding
 

    Transparency declarations
 

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
M. C. Arendrup, G. Garcia-Effron, W. Buzina, K. L. Mortensen, N. Reiter, C. Lundin, H. E. Jensen, C. Lass-Florl, D. S. Perlin, and B. Bruun
Breakthrough Aspergillus fumigatus and Candida albicans Double Infection during Caspofungin Treatment: Laboratory Characteristics and Implication for Susceptibility Testing
Antimicrob. Agents Chemother., March 1, 2009; 53(3): 1185 - 1193.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
G. Garcia-Effron, D. P. Kontoyiannis, R. E. Lewis, and D. S. Perlin
Caspofungin-Resistant Candida tropicalis Strains Causing Breakthrough Fungemia in Patients at High Risk for Hematologic Malignancies
Antimicrob. Agents Chemother., November 1, 2008; 52(11): 4181 - 4183.
[Abstract] [Full Text] [PDF]