Affiliation:
1. Pathology and Laboratory Medicine Service/113, McGuire Veterans Affairs Medical Center, Richmond, Virginia 23249-0001,1 and
2. Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, Nebraska 681782
Abstract
ABSTRACT
AmpC beta-lactamases are cephalosporinases that confer resistance to a wide variety of β-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.
Publisher
American Society for Microbiology
Cited by
172 articles.
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