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Antimicrobial Agents and Chemotherapy, December 1998, p. 3163-3168, Vol. 42, No. 12
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Characterization of a Chromosomal Gene Encoding Type B beta -Lactamase in Phage Group II Isolates of Staphylococcus aureus

Rama Kishan R. Voladri1 and Douglas S. Kernodle1,2,*

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 beta -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 beta -lactamase for which the nucleotide and deduced amino acid sequences have not yet been reported. To better understand beta -lactamase production among phage group II staphylococci and the nature of the type B beta -lactamase, we determined the type and amount of enzyme produced by 24 phage group II isolates. Of these isolates, 1 did not produce beta -lactamase, 8 produced the type B enzyme, and 15 produced the type C enzyme. In all eight type B beta -lactamase-producing isolates, blaZ was located on the chromosome. This was in contrast to the type C beta -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 beta -lactamase that differ from the prototypic type A beta -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 beta -lactamases. In summary, modern isolates of S. aureus typeable by group II phages produce type B or type C staphylococcal beta -lactamase. The type B gene resides on the chromosome and has a sequence that, when compared to the sequences of the other staphylococcal beta -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.


Antimicrobial Agents and Chemotherapy, December 1998, p. 3163-3168, Vol. 42, No. 12
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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