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PMID: 1503440 Published · ppublish English Journal Article

Overproduction of a penicillin-binding protein is not the only mechanism of penicillin resistance in Enterococcus faecium.

Antimicrobial agents and chemotherapy ·Vol. 36 ·No. 4 ·1992-04-00 ·Pages 783-7

Klare I, Rodloff AC, Wagner J, Witte W, Hakenbeck R

Abstract

In 1989 and 1990, a large number of ampicillin-resistant strains of Enterococcus faecium were isolated from infected patients treated at intensive care units in Berlin, Germany. Twenty-five clinical isolates, including five different biotypes as classified by acid production from various sugars and a wide range of susceptibilities to ampicillin (MICs between 0.5 and 128 micrograms/ml), were selected for a detailed analysis of penicillin-binding proteins (PBPs). All strains contained a slowly reacting PBP with low penicillin affinity known to be present in enterococci. Overproduction of this PBP relative to susceptible isolates was noted, especially in all strains for which the MIC of ampicillin was 8 micrograms/ml, to a lesser degree in the more resistant strains, but not at all in the three highly resistant isolates for which the MIC was 128 micrograms/ml. In these three strains, this PBP appears to have a reduced affinity for beta-lactams. The results suggest that overproduction of PBP 6 correlates only with intermediate resistance levels and that higher resistance is mediated by yet another, still unknown mechanism, probably including reduction of beta-lactam affinity in one or more PBPs.

MeSH Terms
Bacterial Proteins Carrier Proteins/biosynthesis Enterococcus faecium/classification,drug effects,metabolism Hexosyltransferases Microbial Sensitivity Tests Muramoylpentapeptide Carboxypeptidase/biosynthesis Penicillin G/metabolism Penicillin Resistance Penicillin-Binding Proteins Penicillins/metabolism Peptidyl Transferases Tritium beta-Lactamases/analysis
Chemicals
Bacterial Proteins Carrier Proteins Penicillin-Binding Proteins Penicillins Tritium Peptidyl Transferases Hexosyltransferases Muramoylpentapeptide Carboxypeptidase beta-Lactamases Penicillin G
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Klare I
Robert-Koch Institut des Bundesgesundheitsamtes, Wernigerode, Germany.
Rodloff A C
Wagner J
Witte W
Hakenbeck R
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1992-04-00
Pages
783-7
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC189409
Subset
IM
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