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Antimicrobial Agents and Chemotherapy, December 1998, p. 3163-3168, Vol. 42, No. 12
Division of Infectious Diseases, Department
of Medicine, Vanderbilt University School of Medicine, Nashville,
Tennessee 37232-2605,1 and
Department of
Veterans Affairs Medical Center, Nashville, Tennessee
37212-26372
Received 9 February 1998/Returned for modification 10 June
1998/Accepted 9 September 1998
In contrast to most Staphylococcus aureus isolates in
which the gene for staphylococcal
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Characterization of a Chromosomal Gene Encoding
Type B
-Lactamase in Phage Group II Isolates of
Staphylococcus aureus
-lactamase (blaZ) is
plasmid borne, isolates typeable by group II bacteriophages frequently
carry blaZ on the chromosome. Furthermore, the chromosomal
gene encodes the type B variant of staphylococcal
-lactamase for
which the nucleotide and deduced amino acid sequences have not yet been reported. To better understand
-lactamase production among phage group II staphylococci and the nature of the type B
-lactamase, we
determined the type and amount of enzyme produced by 24 phage group II
isolates. Of these isolates, 1 did not produce
-lactamase, 8 produced the type B enzyme, and 15 produced the type C enzyme. In all
eight type B
-lactamase-producing isolates, blaZ was
located on the chromosome. This was in contrast to the type C
-lactamase-producing isolates, in which blaZ was located
on a 21-kb plasmid. The nucleotide sequence corresponding to the leader
peptide and the N-terminal 85% of the mature exoenzyme form of type B
S. aureus was determined. The deduced amino acid sequence
revealed 3 residues in the leader peptide and 12 residues in the
exoenzyme portion of the
-lactamase that differ from the prototypic
type A
-lactamase sequence. These include the serine-to-asparagine
change at residue 216 found in the kinetically similar type C enzyme, a
threonine-to-lysine change at residue 128 close to the SDN loop
(residues 130 to 132), and several substitutions not found in any of
the other staphylococcal
-lactamases. In summary, modern isolates of
S. aureus typeable by group II phages produce type B or
type C staphylococcal
-lactamase. The type B gene resides on the
chromosome and has a sequence that, when compared to the sequences of
the other staphylococcal
-lactamases, corresponds well with its
kinetic properties.
*
Corresponding author. Mailing address: Medical Service
(111E), VA Medical Center, 1310 24th Ave. South, Nashville, TN
37212-2637. Phone: (615) 327-4751, ext. 5512. Fax: (615) 321-6327. E-mail: doug.kernodle{at}vanderbilt.edu.
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