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Journal of Clinical Microbiology, December 1999, p. 4065-4070, Vol. 37, No. 12
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Detection and Reporting of Organisms Producing Extended-Spectrum
-Lactamases: Survey of Laboratories in Connecticut
Fred C.
Tenover,1,*
M. Jasmine
Mohammed,1
Timothy S.
Gorton,2 and
Zygmunt
F.
Dembek3
Hospital Infections Program, Centers for
Disease Control and Prevention, Atlanta, Georgia
303331; University of Connecticut,
Department of Pathobiology, Storrs, Connecticut
062692; and Epidemiology Program,
Connecticut Department of Public Health, Hartford, Connecticut
06134-03083
Received 30 June 1999/Returned for modification 5 August
1999/Accepted 1 September 1999
Extended-spectrum
-lactamases (ESBLs) are enzymes produced in
some gram-negative bacilli that mediate resistance to extended-spectrum cephalosporins and aztreonam. They are most common in
Klebsiella spp. and Escherichia coli but are
present in a variety of Enterobacteriaceae. Resistance
mediated by these enzymes can be difficult to detect depending on the
antimicrobial agents tested. AmpC
-lactamases are related to the
chromosomal enzymes of Enterobacter and
Citrobacter spp. and also mediate resistance to
extended-spectrum cephalosporins and aztreonam in addition to
cephamycins, such as cefoxitin. Unlike ESBLs, however, AmpC
-lactamases are not inhibited by clavulanic acid or other similar
compounds. To assess the abilities of various antimicrobial
susceptibility testing methods to detect ESBLs, we sent three
ESBL-producing organisms, one AmpC-producing organism, and a control
strain that was susceptible to extended-spectrum cephalosporins to 38 laboratories in Connecticut for testing. Eight (21.0%) of 38 labs
failed to detect extended-spectrum cephalosporin or aztreonam
resistance in any of the ESBL- or AmpC-producing isolates. Errors were
encountered with both automated and disk diffusion methods. Conversely,
seven (18.4%) labs categorized at least some of the four resistant
isolates as potential ESBL producers and reported the results with the
extended-spectrum cephalosporins and aztreonam as resistant as
suggested by current National Committee for Clinical Laboratory
Standards (NCCLS) guidelines. The percentage of laboratories that
failed to detect resistance in the ESBL or AmpC isolates ranged from
23.7 to 31.6% depending on the type of enzyme present in the test
organism. This survey suggests that many laboratories have difficulty
detecting resistance in ESBL and AmpC-producing organisms and may be
unaware of the NCCLS guidelines on modifying susceptibility testing
reports for ESBL-producing strains.
*
Corresponding author. Mailing address: Nosocomial
Pathogens Laboratory Branch (G08), Hospital Infections Program, Centers for Disease Control and Prevention, 1600 Clifton Rd., Atlanta, GA
30333. Phone: (404) 639-3246. Fax: (404) 639-1381. E-mail: fnt1{at}CDC.GOV.
Journal of Clinical Microbiology, December 1999, p. 4065-4070, Vol. 37, No. 12
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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