|
|
||||||||
1HBpital Saint-Joseph, Service de Microbiologie Clinique, 185 rue Raymond Losserand, 75674 Paris Cedex 14, France
2LRMA, Universite Paris VI, 15, rue de I'Ecole de MCdecine, 75270 Paris Cedex 06, France
3Physics Department, Roussel UCLAF, 93230 Romainville, France
1 Author for correspondence: Jean-Luc Mainardi. Tel: +33 1 42 34 68 63. Fax: +33 1 43 25 68 12
ABSTRACT
SUMMARY: The influence of NaCl on the susceptibility of Enterococcus faecalis to cefotaxime was tested with JH2-2, a laboratory strain, and 20 clinical strains grown on tryptic soy agar supplemented with 5% horse blood. Growth with 3% NaCl in the medium resulted in an increase in cefotaxime resistance and the appearance of a heterogeneous resistance phenotype: for the majority of the strains, the MlCs of cefotaxime increased from 4 to 512 pg m1-Y By a competition assay using cefotaxime and [3H]benzylpenicillin, it was shown for strain JH2-2 that at the MIC penicillin-binding protein (PBP) 2 and PBP3 were the apparent essential PBPs in medium without NaCI, whilst the low-affinity PBPs 4 and 1 were the apparent essential PBPs for cell growth in medium containing 3% NaCl. Analysis of JH2-2 peptidoglycan by HPLC and MS after growth in the presence of 3% NaCl showed a relative increase in unsubstituted monomers and a relative decrease in alanine- and dialanine-substituted monomers. It is therefore hypothesized that modification of the number of alanine-substituted precursors in the presence of NaCl could interfere with the functions of the different PBPs and thus play a role in cefotaxime resistance in E. faecalis.
This article has been cited by other articles:
![]() |
J. van Heijenoort Lipid Intermediates in the Biosynthesis of Bacterial Peptidoglycan Microbiol. Mol. Biol. Rev., December 1, 2007; 71(4): 620 - 635. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Hebert, P. Courtin, R. Torelli, M. Sanguinetti, M.-P. Chapot-Chartier, Y. Auffray, and A. Benachour Enterococcus faecalis Constitutes an Unusual Bacterial Model in Lysozyme Resistance Infect. Immun., November 1, 2007; 75(11): 5390 - 5398. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. David, B. Bozdogan, J.-L. Mainardi, R. Legrand, L. Gutmann, and R. Leclercq Mechanism of Intrinsic Resistance to Vancomycin in Clostridium innocuum NCIB 10674 J. Bacteriol., June 1, 2004; 186(11): 3415 - 3422. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Bouhss, N. Josseaume, A. Severin, K. Tabei, J.-E. Hugonnet, D. Shlaes, D. Mengin-Lecreulx, J. van Heijenoort, and M. Arthur Synthesis of the L-Alanyl-L-alanine Cross-bridge of Enterococcus faecalis Peptidoglycan J. Biol. Chem., November 22, 2002; 277(48): 45935 - 45941. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Duez, W. Zorzi, F. Sapunaric, A. Amoroso, I. Thamm, and J. Coyette The penicillin resistance of Enterococcus faecalis JH2-2r results from an overproduction of the low-affinity penicillin-binding protein PBP4 and does not involve a psr-like gene Microbiology, September 1, 2001; 147(9): 2561 - 2569. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Grohs, L. Gutmann, R. Legrand, B. Schoot, and J. L. Mainardi Vancomycin Resistance Is Associated with Serine-Containing Peptidoglycan in Enterococcus gallinarum J. Bacteriol., November 1, 2000; 182(21): 6228 - 6232. [Abstract] [Full Text] |
||||
![]() |
J. van Heijenoort and L. Gutmann Correlation between the structure of the bacterial peptidoglycan monomer unit, the specificity of transpeptidation, and susceptibility to beta -lactams PNAS, May 9, 2000; 97(10): 5028 - 5030. [Full Text] [PDF] |
||||
![]() |
J.-L. Mainardi, R. Legrand, M. Arthur, B. Schoot, J. van Heijenoort, and L. Gutmann Novel Mechanism of beta -Lactam Resistance Due to Bypass of DD-Transpeptidation in Enterococcus faecium J. Biol. Chem., May 26, 2000; 275(22): 16490 - 16496. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |