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Journal of Clinical Microbiology, May 2000, p. 1791-1796, Vol. 38, No. 5
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Occurrence and Detection of AmpC Beta-Lactamases
among Escherichia coli, Klebsiella pneumoniae,
and Proteus mirabilis Isolates at a Veterans Medical
Center
Philip E.
Coudron,1,*
Ellen S.
Moland,2 and
Kenneth
S.
Thomson2
Pathology and Laboratory Medicine
Service/113, McGuire Veterans Affairs Medical Center, Richmond,
Virginia 23249-0001,1 and Department of
Medical Microbiology and Immunology, Creighton University School of
Medicine, Omaha, Nebraska 681782
Received 21 September 1999/Returned for modification 26 November
1999/Accepted 18 February 2000
AmpC beta-lactamases are cephalosporinases that confer resistance
to a wide variety of
-lactam drugs and that may thereby create
serious therapeutic problems. Although reported with increasing frequency, the true rate of occurrence of AmpC beta-lactamases in
Escherichia coli, Klebsiella pneumoniae, and
Proteus mirabilis remains unknown. We tested a total of
1,286 consecutive, nonrepeat isolates of these three species and found
that, overall, 45 (3.5%) yielded a cefoxitin zone diameter less than
18 mm (screen positive) and that 16 (1.2%) demonstrated AmpC bands by
isoelectric focusing. Based on the species, of 683 E. coli,
371 K. pneumoniae, and 232 P. mirabilis
isolates tested, 13 (1.9%), 28 (7.6%), and 4 (1.7%), respectively,
demonstrated decreased zone diameters and 11 (1.6%), 4 (1.1%), and 1 (0.4%), respectively, demonstrated AmpC bands. Cefoxitin resistance
was transferred for all but 8 (E. coli) of the 16 AmpC
producers. We also describe a three-dimensional extract test, which was
used to detect phenotypically isolates that harbor AmpC beta-lactamase.
Of the 45 cefoxitin-resistant isolates, the three-dimensional extract
test accurately identified all 16 AmpC producers and 28 of 29 (97%)
isolates as non-AmpC producers. Interestingly, most (86%) isolates in
the latter group were K. pneumoniae isolates. These data
confirm that, at our institution, E. coli, K. pneumoniae, and P. mirabilis harbor plasmid-mediated
AmpC enzymes.
*
Corresponding author. Mailing address: Pathology and
Laboratory Medicine Service/113, McGuire Veterans Affairs Medical
Center, 1201 Broad Rock Blvd., Richmond, VA 23249-0001. Phone: (804)
675-5809. Fax: (804) 675-5518. E-mail:
Philip.Coudron{at}med.va.gov.
Journal of Clinical Microbiology, May 2000, p. 1791-1796, Vol. 38, No. 5
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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