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Journal of Clinical Microbiology, February 2003, p. 772-777, Vol. 41, No. 2
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.2.772-777.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Occurrence of Extended-Spectrum and AmpC Beta-Lactamases in Bloodstream Isolates of Klebsiella pneumoniae: Isolates Harbor Plasmid-Mediated FOX-5 and ACT-1 AmpC Beta-Lactamases

Philip E. Coudron,1* Nancy D. Hanson,2 and Michael W. Climo3

Pathology and Laboratory Medicine Service/113,1 Department of Medicine, McGuire Veterans Affairs Medical Center, Richmond, Virginia 23249-0001,3 Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, Nebraska 681782

Received 12 August 2002/ Returned for modification 4 October 2002/ Accepted 12 November 2002

We tested 190 Klebsiella pneumoniae bloodstream isolates recovered from 189 patients in 30 U.S. hospitals in 23 states to determine the occurrence of extended-spectrum ß-lactamase (ESBL) and AmpC ß-lactamase producers. Based on growth inhibition by clavulanic acid by disk and MIC test methods, 18 (9.5%) of the isolates produced ESBLs. Although the disk diffusion method with standard breakpoints identified 28 cefoxitin-nonsusceptible isolates, only 5 (18%) of these were confirmed as AmpC producers. Of two AmpC confirmatory tests, the three-dimensional extract test was easier to perform than was the double-disk approximation test using a novel inhibitor, Syn2190. Three of the five AmpC producers carried the blaFOX-5 gene, while the other two isolates harbored the blaACT-1 gene. All AmpC genes were transferable. In vitro susceptibility testing with standard inocula showed that all five AmpC-producing strains were susceptible to cefepime, imipenem, and ertapenem but that with a high inoculum, more of these strains were susceptible to the carbapenems than to cefepime. All but 1 of 14 screen-positive AmpC nonproducers (and ESBL nonproducers) were susceptible to ceftriaxone and cefepime at the standard inoculum as were 6 of 6 isolates that were randomly selected and tested with a high inoculum. These results indicate that (i) a significant number of K. pneumoniae bloodstream isolates harbor ESBL or AmpC ß-lactamases, (ii) confirmatory tests are necessary to identify true AmpC producers, and (iii) in vitro, carbapenems are active against AmpC-producing strains of K. pneumoniae.


* Corresponding author. Mailing address: Pathology & 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, February 2003, p. 772-777, Vol. 41, No. 2
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.2.772-777.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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