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 Chanal, C.
Right arrow Articles by Sirot, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chanal, C.
Right arrow Articles by Sirot, J.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, July 2000, p. 1930-1935, Vol. 44, No. 7
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Prevalence of beta -Lactamases among 1,072 Clinical Strains of Proteus mirabilis: a 2-Year Survey in a French Hospital

C. Chanal,1,* R. Bonnet,1 C. De Champs,1 D. Sirot,1 R. Labia,2 and J. Sirot1

Laboratoire de Bactériologie, Faculté de Médecine, 63001 Clermont-Ferrand Cedex,1 and UMR 175, CNRS-MNHN, 29000 Quimper,2 France

Received 27 September 1999/Returned for modification 22 February 2000/Accepted 12 April 2000

beta -Lactam resistance was studied in 1,072 consecutive P. mirabilis clinical strains isolated at the Clermont-Ferrand teaching hospital between April 1996 and March 1998. The frequency of amoxicillin resistance was 48.5%. Among the 520 amoxicillin-resistant isolates, three resistance phenotypes were detected: penicillinase (407 strains [78.3%]), extended-spectrum beta -lactamase (74 strains [14.2%]), and inhibitor resistance (39 strains [7.5%]). The penicillinase phenotype isolates were divided into three groups according to the level of resistance to beta -lactams, which was shown to be related to the strength of the promoter. The characterization of the different beta -lactamases showed that amoxicillin resistance in P. mirabilis was almost always (97%) associated with TEM or TEM-derived beta -lactamases, most of which evolved via TEM-2.


* Corresponding author. Mailing address: Laboratoire de Bactériologie, Faculté de Médecine, 28, Place Henri Dunant, 63001 Clermont-Ferrand Cedex, France. Phone: 33 (0)4 73 60 80 18. Fax: 33 (0)4 73 27 74 94. E. mail: Catherine.CHANAL{at}u-clermont1.fr.


Antimicrobial Agents and Chemotherapy, July 2000, p. 1930-1935, Vol. 44, No. 7
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Savini, V., Catavitello, C., Talia, M., Di Berardino, F., Manna, A., Balbinot, A., Febbo, F., Carlino, D., Fioritoni, F., Di Bonaventura, G., D'Antonio, D. (2008). Ulcer Infection by ES{beta}L-Producing Proteus mirabilis: A Case Report. INT J LOW EXTREM WOUNDS 7: 99-101 [Abstract]  
  • Aragon, L. M., Mirelis, B., Miro, E., Mata, C., Gomez, L., Rivera, A., Coll, P., Navarro, F. (2008). Increase in {beta}-lactam-resistant Proteus mirabilis strains due to CTX-M- and CMY-type as well as new VEB- and inhibitor-resistant TEM-type {beta}-lactamases. J Antimicrob Chemother 61: 1029-1032 [Abstract] [Full Text]  
  • Park, Y.-J., Lee, S., Kim, Y. R., Oh, E.-J., Woo, G.-J., Lee, K. (2006). Occurrence of extended-spectrum {beta}-lactamases and plasmid-mediated AmpC {beta}-lactamases among Korean isolates of Proteus mirabilis. J Antimicrob Chemother 57: 156-158 [Full Text]  
  • Literacka, E., Empel, J., Baraniak, A., Sadowy, E., Hryniewicz, W., Gniadkowski, M. (2004). Four Variants of the Citrobacter freundii AmpC-Type Cephalosporinases, Including Novel Enzymes CMY-14 and CMY-15, in a Proteus mirabilis Clone Widespread in Poland. Antimicrob. Agents Chemother. 48: 4136-4143 [Abstract] [Full Text]  
  • Nagano, N., Shibata, N., Saitou, Y., Nagano, Y., Arakawa, Y. (2003). Nosocomial Outbreak of Infections by Proteus mirabilis That Produces Extended-Spectrum CTX-M-2 Type {beta}-Lactamase. J. Clin. Microbiol. 41: 5530-5536 [Abstract] [Full Text]  
  • Barlow, M., Hall, B. G. (2003). Experimental Prediction of the Natural Evolution of Antibiotic Resistance. Genetics 163: 1237-1241 [Abstract] [Full Text]  
  • Naas, T., Zerbib, M., Girlich, D., Nordmann, P. (2003). Integration of a Transposon Tn1-Encoded Inhibitor-Resistant {beta}-Lactamase Gene, blaTEM-67 from Proteus mirabilis, into the Escherichia coli Chromosome. Antimicrob. Agents Chemother. 47: 19-26 [Abstract] [Full Text]  
  • Mutnick, A. H, Kirby, J. T, Jones, R. N (2003). CANCER Resistance Surveillance Program: Initial Results from Hematology-Oncology Centers in North America. The Annals of Pharmacotherapy 37: 47-56 [Abstract] [Full Text]  
  • Miro, E., Navarro, F., Mirelis, B., Sabate, M., Rivera, A., Coll, P., Prats, G. (2002). Prevalence of Clinical Isolates of Escherichia coli Producing Inhibitor-Resistant {beta}-Lactamases at a University Hospital in Barcelona, Spain, over a 3-Year Period. Antimicrob. Agents Chemother. 46: 3991-3994 [Abstract] [Full Text]  
  • Bonnet, R., Marchandin, H., Chanal, C., Sirot, D., Labia, R., De Champs, C., Jumas-Bilak, E., Sirot, J. (2002). Chromosome-Encoded Class D {beta}-Lactamase OXA-23 in Proteus mirabilis. Antimicrob. Agents Chemother. 46: 2004-2006 [Abstract] [Full Text]  
  • Pagani, L., Migliavacca, R., Pallecchi, L., Matti, C., Giacobone, E., Amicosante, G., Romero, E., Rossolini, G. M. (2002). Emerging Extended-Spectrum {beta}-Lactamases in Proteus mirabilis. J. Clin. Microbiol. 40: 1549-1552 [Abstract] [Full Text]  
  • Barlow, M., Hall, B. G. (2002). Predicting Evolutionary Potential: In Vitro Evolution Accurately Reproduces Natural Evolution of the TEM {beta}-Lactamase. Genetics 160: 823-832 [Abstract] [Full Text]