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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