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 Segura, C.
Right arrow Articles by Coira, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Segura, C.
Right arrow Articles by Coira, A.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, June 1998, p. 1524-1526, Vol. 42, No. 6
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Contribution of beta -Lactamases to beta -Lactam Susceptibilities of Susceptible and Multidrug-Resistant Mycobacterium tuberculosis Clinical Isolates

C. Segura,1,2,* M. Salvadó,1,2 I. Collado,3 J. Chaves,3 and A. Coira3

Laboratori de Referència de Catalunya1 and Departament de Genética y Microbiología,2 Universitat Autònoma de Barcelona, and Institut Municipal d'Investigació Mèdica,3 Barcelona, Spain

Received 4 September 1997/Returned for modification 18 December 1997/Accepted 24 March 1998

The beta -lactamases in 154 clinical Mycobacterium tuberculosis strains were studied. Susceptibilities to beta -lactam antibiotics, their combination with clavulanate (2:1), and two fluoroquinolones were determined in 24 M. tuberculosis strains susceptible to antimycobacterial drugs and in nine multiresistant strains. All 154 M. tuberculosis isolates showed a single chromosomal beta -lactamase pattern (pI 4.9 and 5.1). M. tuberculosis beta -lactamase hydrolyzes cefotaxime with a maximum rate of 22.5 ± 2.19 IU/liter (strain 1382). Neither amoxicillin, carbenicillin, cefotaxime, ceftriaxone, nor aztreonam was active alone. Except for aztreonam, beta -lactam combinations with clavulanate produced better antimycobacterial activity.


* Corresponding author. Mailing address: Cerdeña 257, 3o 1a, Barcelona 08013, Spain. Phone: (34)-3-2630920. Fax: (34)-3-2630671. E-mail: msalvador{at}lrc.es.


Antimicrobial Agents and Chemotherapy, June 1998, p. 1524-1526, Vol. 42, No. 6
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Hugonnet, J.-E., Tremblay, L. W., Boshoff, H. I., Barry, C. E. 3rd, Blanchard, J. S. (2009). Meropenem-Clavulanate Is Effective Against Extensively Drug-Resistant Mycobacterium tuberculosis. Science 323: 1215-1218 [Abstract] [Full Text]  
  • Wang, F., Cassidy, C., Sacchettini, J. C. (2006). Crystal Structure and Activity Studies of the Mycobacterium tuberculosis {beta}-Lactamase Reveal Its Critical Role in Resistance to {beta}-Lactam Antibiotics.. Antimicrob. Agents Chemother. 50: 2762-2771 [Abstract] [Full Text]  
  • Flores, A. R., Parsons, L. M., Pavelka,, M. S. Jr (2005). Genetic analysis of the {beta}-lactamases of Mycobacterium tuberculosis and Mycobacterium smegmatis and susceptibility to {beta}-lactam antibiotics. Microbiology 151: 521-532 [Abstract] [Full Text]  
  • Philalay, J. S., Palermo, C. O., Hauge, K. A., Rustad, T. R., Cangelosi, G. A. (2004). Genes Required for Intrinsic Multidrug Resistance in Mycobacterium avium. Antimicrob. Agents Chemother. 48: 3412-3418 [Abstract] [Full Text]