Affiliation:
1. The Rockefeller University, New York
2. Wyeth, Pearl River, New York
Abstract
ABSTRACT
A combination of biochemical and genetic experiments were performed in order to better understand the mechanism of expression of high-level vancomycin resistance in
Staphylococcus aureus
. The transcription of
pbp2
of the highly vancomycin- and oxacillin-resistant strain COLVA
200
and its mutant derivative with inactivated
mecA
were put under the control of an inducible promoter, and the dependence of oxacillin and vancomycin resistance and cell wall composition on the concentration of the isopropyl-β-
d
-thiogalactopyranoside inducer was determined. The results indicate that
mecA—
the genetic determinant of oxacillin resistance—while essential for oxacillin resistance, is not involved with the expression of vancomycin resistance. Penicillin binding protein 2A, the protein product of
mecA
, appears to be unable to utilize the depsipeptide cell wall precursor produced in the vancomycin-resistant cells for transpeptidation. The key penicillin binding protein essential for vancomycin resistance and for the synthesis of the abnormally structured cell walls characteristic of vancomycin-resistant
S. aureus
(A. Severin, K. Tabei, F. Tenover, M. Chung, N. Clarke, and A. Tomasz, J. Biol. Chem.
279
:3398-3407, 2004) is penicillin binding protein 2.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
49 articles.
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