Journal of Antimicrobial Chemotherapy, Vol 42, 315-320, Copyright © 1998 by The British Society for Antimicrobial Chemotherapy
H Hanaki, H Labischinski, Y Inaba, N Kondo, H Murakami and K Hiramatsu
The peptidoglycan compositions of vancomycin-resistant Staphylococcus
aureus (VRSA) strain Mu50 (MIC 8 mg/L) and hetero-VRSA strain Mu3 (MIC 3
mg/L) were compared in order to understand the mechanism of vancomycin
resistance. As compared with Mu3, the cell wall of Mu50 had increased
amounts of glutamine-non-amidated muropeptides and decreased cross-linking
of peptidoglycan with a greatly decreased dimer/monomer ratio of
muropeptides. In agreement with this observation, the peptidoglycan of Mu50
bound 1.4 times more vancomycin than that of Mu3. The increase in
non-amidated muropeptides and the reduced cross-linking of the cell-wall
peptidoglycan may contribute to the vancomycin resistance by increasing the
consumption of vancomycin by the pre- existing cell wall of Mu50 and
reducing the amount of vancomycin reaching the cytoplasmic membrane where
the vital targets of the antibiotic are situated.
ORIGINAL ARTICLES
Increase in glutamine-non-amidated muropeptides in the peptidoglycan of vancomycin-resistant Staphylococcus aureus strain Mu50
Department of Bacteriology, Juntendo University, Tokyo, Japan.
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