This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Barnaud, G.
Right arrow Articles by Arlet, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Barnaud, G.
Right arrow Articles by Arlet, G.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, March 2004, p. 1040-1042, Vol. 48, No. 3
0066-4804/04/$08.00+0     DOI: 10.1128/AAC.48.3.1040-1042.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Selection during Cefepime Treatment of a New Cephalosporinase Variant with Extended-Spectrum Resistance to Cefepime in an Enterobacter aerogenes Clinical Isolate

G. Barnaud,1,2* Y. Benzerara,1 J. Gravisse,2 L. Raskine,2 M. J. Sanson-Le Pors,2 R. Labia,3 and G. Arlet1

Service de Bactériologie, Hôpital Tenon AP-HP,1 Service de Bactériologie-Virologie, Hôpital Lariboisière AP-HP, Paris,2 CNRS-UBO-MNHN, Unité FRE 2125, Quimper, France3

Received 23 May 2003/ Returned for modification 22 July 2003/ Accepted 11 November 2003

Enterobacter aerogenes resistant to cefepime (MIC, 32 µg/ml) was isolated from a patient treated with cefepime for an infection caused by a strain of E. aerogenes overproducing its AmpC ß-lactamase (MIC of cefepime, 0.5 µg/ml). The AmpC ß-lactamase of the resistant strain had an L-293-P amino acid substitution and a high kcat/Km ratio for cefepime. Both of these modifications were necessary for resistance to cefepime.


* Corresponding author. Mailing address: Service de Microbiologie et Hygiène, Hôpital Louis-Mourier AP-HP, 178 rue des Renouillers, 92701 Colombes Cedex, France. Phone: 33 1 47 60 60 10. Fax: 33 1 47 60 60 48. E-mail: guilene.barnaud{at}lmr.ap-hop-paris.fr.


Antimicrobial Agents and Chemotherapy, March 2004, p. 1040-1042, Vol. 48, No. 3
0066-4804/04/$08.00+0     DOI: 10.1128/AAC.48.3.1040-1042.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Doi, Y., Paterson, D. L., Adams-Haduch, J. M., Sidjabat, H. E., O'Keefe, A., Endimiani, A., Bonomo, R. A. (2009). Reduced Susceptibility to Cefepime among Escherichia coli Clinical Isolates Producing Novel Variants of CMY-2 {beta}-Lactamase. Antimicrob. Agents Chemother. 53: 3159-3161 [Abstract] [Full Text]  
  • Rodriguez-Martinez, J.-M., Poirel, L., Nordmann, P. (2009). Extended-Spectrum Cephalosporinases in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 53: 1766-1771 [Abstract] [Full Text]  
  • Tran, Q.-T., Dupont, M., Lavigne, J.-P., Chevalier, J., Pages, J.-M., Sotto, A., Davin-Regli, A. (2009). Occurrence of Efflux Mechanism and Cephalosporinase Variant in a Population of Enterobacter aerogenes and Klebsiella pneumoniae Isolates Producing Extended-Spectrum {beta}-Lactamases. Antimicrob. Agents Chemother. 53: 1652-1656 [Abstract] [Full Text]  
  • Petersen, P. J., Jones, C. H., Venkatesan, A. M., Bradford, P. A. (2009). Efficacy of Piperacillin Combined with the Penem {beta}-Lactamase Inhibitor BLI-489 in Murine Models of Systemic Infection. Antimicrob. Agents Chemother. 53: 1698-1700 [Abstract] [Full Text]  
  • Petersen, P. J., Jones, C. H., Venkatesan, A. M., Mansour, T. S., Projan, S. J., Bradford, P. A. (2009). Establishment of In Vitro Susceptibility Testing Methodologies and Comparative Activities of Piperacillin in Combination with the Penem {beta}-Lactamase Inhibitor BLI-489. Antimicrob. Agents Chemother. 53: 370-384 [Abstract] [Full Text]  
  • Jacoby, G. A. (2009). AmpC {beta}-Lactamases. Clin. Microbiol. Rev. 22: 161-182 [Abstract] [Full Text]  
  • Hee Lee, S., Lee, J. H., Heo, M. J., Bae, I. K., Jeong, S. H., Cha, S.-S., Wachino, J.-i., Arakawa, Y. (2007). Exact Location of the Region Responsible for the Extended Substrate Spectrum in Class C {beta}-Lactamases. Antimicrob. Agents Chemother. 51: 3778-3779 [Full Text]  
  • Mammeri, H., Poirel, L., Nordmann, P. (2007). Extension of the hydrolysis spectrum of AmpC {beta}-lactamase of Escherichia coli due to amino acid insertion in the H-10 helix. J Antimicrob Chemother 60: 490-494 [Abstract] [Full Text]  
  • Wachino, J.-i., Kurokawa, H., Suzuki, S., Yamane, K., Shibata, N., Kimura, K., Ike, Y., Arakawa, Y. (2006). Horizontal Transfer of blaCMY-Bearing Plasmids among Clinical Escherichia coli and Klebsiella pneumoniae Isolates and Emergence of Cefepime-Hydrolyzing CMY-19. Antimicrob. Agents Chemother. 50: 534-541 [Abstract] [Full Text]  
  • Hidri, N., Barnaud, G., Decre, D., Cerceau, C., Lalande, V., Petit, J. C., Labia, R., Arlet, G. (2005). Resistance to ceftazidime is associated with a S220Y substitution in the omega loop of the AmpC {beta}-lactamase of a Serratia marcescens clinical isolate. J Antimicrob Chemother 55: 496-499 [Abstract] [Full Text]