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Journal of Clinical Microbiology, September 2006, p. 3257-3262, Vol. 44, No. 9
0095-1137/06/$08.00+0     doi:10.1128/JCM.00433-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Evaluation of the New VITEK 2 Extended-Spectrum Beta-Lactamase (ESBL) Test for Rapid Detection of ESBL Production in Enterobacteriaceae Isolates

Teresa Spanu,1* Maurizio Sanguinetti,1 Mario Tumbarello,2 Tiziana D'Inzeo,1 Barbara Fiori,1 Brunella Posteraro,1 Rosaria Santangelo,1 Roberto Cauda,2 and Giovanni Fadda1

Institute of Microbiology,1 Department of Infectious Diseases, Catholic University of the Sacred Heart, Rome, Italy2

Received 28 February 2006/ Returned for modification 23 March 2006/ Accepted 7 July 2006

Extended-spectrum beta-lactamases (ESBLs) are a large, rapidly evolving group of enzymes that confer resistance to oxyimino cephalosporins and monobactams and are inhibited by clavulanate. Rapid reliable detection of ESBL production is a prerequisite for successful infection management and for monitoring resistance trends and implementation of intervention strategies. We evaluated the performance of the new VITEK 2 ESBL test system (bioMérieux, Inc, Hazelwood, Mo.) in the identification of ESBL-producing Enterobacteriaceae isolates. We examined a total of 1,129 clinically relevant Enterobacteriaceae isolates (including 218 that had been previously characterized). The ESBL classification furnished by the VITEK 2 ESBL test system was concordant with that of the comparison method (molecular identification of beta-lactamase genes) for 1,121 (99.3%) of the 1,129 isolates evaluated. ESBL production was correctly detected in 306 of the 312 ESBL-producing organisms (sensitivity, 98.1%; positive predictive value, 99.3%). False-positive results emerged for 2 of the 817 ESBL-negative isolates (specificity, 99.7%; negative predictive value, 99.3%). VITEK 2 ESBL testing took 6 to 13 h (median, 7.5 h; mean ± SD, 8.2 ± 2.39 h). This automated short-incubation system appears to be a rapid and reliable tool for routine identification of ESBL-producing isolates of Enterobacteriaceae.


* Corresponding author. Mailing address: Istituto Microbiologia, Università Cattolica del Sacro Cuore, Largo A. Gemelli 8, 00168 Roma, Italy. Phone: 39-06-30154218. Fax: 39-06-3051152. E-mail: tspanu{at}rm.unicatt.it.


Journal of Clinical Microbiology, September 2006, p. 3257-3262, Vol. 44, No. 9
0095-1137/06/$08.00+0     doi:10.1128/JCM.00433-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Thomson, K. S., Cornish, N. E., Hong, S. G., Hemrick, K., Herdt, C., Moland, E. S. (2007). Comparison of Phoenix and VITEK 2 Extended-Spectrum-{beta}-Lactamase Detection Tests for Analysis of Escherichia coli and Klebsiella Isolates with Well-Characterized {beta}-Lactamases. J. Clin. Microbiol. 45: 2380-2384 [Abstract] [Full Text]  
  • Tumbarello, M., Sanguinetti, M., Montuori, E., Trecarichi, E. M., Posteraro, B., Fiori, B., Citton, R., D'Inzeo, T., Fadda, G., Cauda, R., Spanu, T. (2007). Predictors of Mortality in Patients with Bloodstream Infections Caused by Extended-Spectrum-{beta}-Lactamase-Producing Enterobacteriaceae: Importance of Inadequate Initial Antimicrobial Treatment. Antimicrob. Agents Chemother. 51: 1987-1994 [Abstract] [Full Text]