J Med Microbiol Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
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 PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R. J.
Right arrow Articles by Williams, J. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Williams, R. J.
Right arrow Articles by Williams, J. D.
Agricola
Right arrow Articles by Williams, R. J.
Right arrow Articles by Williams, J. D.

The Journal of Medical Microbiology, Vol 17, Issue 3 283-293, Copyright © 1984 by Society for General Microbiology


JOURNAL ARTICLE

Mechanisms of beta-lactam resistance in British isolates of Pseudomonas aeruginosa

R. J. Williams, D. M. Livermore, M. A. Lindridge, A. A. Said and J. D. Williams

The mechanisms of resistance to beta-lactam antibiotics in 191 isolates of Pseudomonas aeruginosa were examined. These represented the most resistant organisms of 1866 isolates collected during a national survey of antibiotic resistance in this species. One hundred and seventy-two isolates were selected because they were resistant to carbenicillin (MIC greater than 128 mg/L) and 19 because the MICs of cefotaxime were greater than the MICs of carbenicillin. Of the carbenicillin-resistant isolates, 35 produced plasmid-mediated beta-lactamases known to be active against carbenicillin and seven produced unusual beta-lactamases; in 131 strains, resistance could not be attributed to beta-lactamase production and was considered to be intrinsic. The unusual antibiogram in which the MIC of cefotaxime was greater than the MIC of carbenicillin was associated with overproduction of the chromosomally-determined Sabath and Abrahams ' beta-lactamase. Selection of strains with this last mechanism represents a novel resistance problem and one which may increase with increased use of newer antipseudomonal beta-lactams.


This article has been cited by other articles:


Home page
Clin. Microbiol. Rev.Home page
P. Gilbert and A. J. McBain
Potential Impact of Increased Use of Biocides in Consumer Products on Prevalence of Antibiotic Resistance
Clin. Microbiol. Rev., April 1, 2003; 16(2): 189 - 208.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
J. D. Cavallo, P. Plesiat, G. Couetdic, F. Leblanc, R. Fabre, and Groupe d'Etude de la Resistance de Pseudomonas aer
Mechanisms of {beta}-lactam resistance in Pseudomonas aeruginosa: prevalence of OprM-overproducing strains in a French multicentre study (1997)
J. Antimicrob. Chemother., December 1, 2002; 50(6): 1039 - 1043.
[Abstract] [Full Text] [PDF]


Home page
Protein Eng Des SelHome page
A. Savoie, F. Sanschagrin, T. Palzkill, N. Voyer, and R. C. Levesque
Structure-function analysis of {alpha}-helix H4 using PSE-4 as a model enzyme representative of class A {beta}-lactamases
Protein Eng. Des. Sel., April 1, 2000; 13(4): 267 - 274.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
I. Ziha-Zarifi, C. Llanes, T. Köhler, J.-C. Pechere, and P. Plesiat
In Vivo Emergence of Multidrug-Resistant Mutants of Pseudomonas aeruginosa Overexpressing the Active Efflux System MexA-MexB-OprM
Antimicrob. Agents Chemother., February 1, 1999; 43(2): 287 - 291.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 1984 Society for General Microbiology.