This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jayaratne, P.
Right arrow Articles by Rutherford, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jayaratne, P.
Right arrow Articles by Rutherford, C.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, June 1999, p. 2090-2092, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Detection of Clinically Relevant Genotypes of Vancomycin-Resistant Enterococci in Nosocomial Surveillance Specimens by PCR

P. Jayaratne1,2,* and C. Rutherford2

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada L8N 3Z5,1 and Microbiology Section, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences Corporation, General Campus, Hamilton, Ontario, Canada L8L 2X22

Received 2 December 1998/Returned for modification 22 January 1999/Accepted 17 March 1999

This study evaluated a PCR method for the rapid detection of clinically significant genotypes of vancomycin-resistant enterococci (VRE) in nosocomial surveillance specimens. Detection of the vanA and vanB genes by multiplex PCR using 657 specimens that showed presumptive growth of VRE on bile esculin azide agar containing 6 mg of vancomycin/liter was compared to the conventional method. The diagnostic values for the PCR compared to the phenotypic method were as follows: 99.8% specificity, 95.4% sensitivity, 98.8% positive predictive value, and 99.3% negative predictive value. The average cost per test for PCR is $8.26, compared to $9.45 for the phenotypic method. The average turnaround time for detecting a VRE is 48 h for PCR, compared to 96 h for the conventional method.


* Corresponding author. Mailing address: Microbiology Section, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences Corporation, General Campus, 237 Barton St. East, Hamilton, Ontario, Canada, L8L 2X2. Phone: (905) 527-4322, ext. 6182. Fax: (905) 577-8027. E-mail: Jayaratn{at}FHS.McMaster.CA.


Journal of Clinical Microbiology, June 1999, p. 2090-2092, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Eigner, U., Fahr, A., Weizenegger, M., Witte, W. (2005). Evaluation of a New Molecular System for Simultaneous Identification of Four Enterococcus Species and Their Glycopeptide Resistance Genotypes. J. Clin. Microbiol. 43: 2920-2922 [Abstract] [Full Text]  
  • Ballard, S. A., Grabsch, E. A., Johnson, P. D. R., Grayson, M. L. (2005). Comparison of Three PCR Primer Sets for Identification of vanB Gene Carriage in Feces and Correlation with Carriage of Vancomycin-Resistant Enterococci: Interference by vanB-Containing Anaerobic Bacilli. Antimicrob. Agents Chemother. 49: 77-81 [Abstract] [Full Text]  
  • Depardieu, F., Perichon, B., Courvalin, P. (2004). Detection of the van Alphabet and Identification of Enterococci and Staphylococci at the Species Level by Multiplex PCR. J. Clin. Microbiol. 42: 5857-5860 [Abstract] [Full Text]  
  • Novicki, T. J., Schapiro, J. M., Ulness, B. K., Sebeste, A., Busse-Johnston, L., Swanson, K. M., Swanzy, S. R., Leisenring, W., Limaye, A. P. (2004). Convenient Selective Differential Broth for Isolation of Vancomycin-Resistant Enterococcus from Fecal Material. J. Clin. Microbiol. 42: 1637-1640 [Abstract] [Full Text]  
  • Palladino, S., Kay, I. D., Flexman, J. P., Boehm, I., Costa, A. M. G., Lambert, E. J., Christiansen, K. J. (2003). Rapid Detection of vanA and vanB Genes Directly from Clinical Specimens and Enrichment Broths by Real-Time Multiplex PCR Assay. J. Clin. Microbiol. 41: 2483-2486 [Abstract] [Full Text]  
  • Brown, D. F. J., Walpole, E. (2003). Evaluation of selective and enrichment media for isolation of glycopeptide-resistant enterococci from faecal specimens. J Antimicrob Chemother 51: 289-296 [Abstract] [Full Text]  
  • Angeletti, S., Lorino, G., Gherardi, G., Battistoni, F., De Cesaris, M., Dicuonzo, G. (2001). Routine Molecular Identification of Enterococci by Gene-Specific PCR and 16S Ribosomal DNA Sequencing. J. Clin. Microbiol. 39: 794-797 [Abstract] [Full Text]  
  • Kariyama, R., Mitsuhata, R., Chow, J. W., Clewell, D. B., Kumon, H. (2000). Simple and Reliable Multiplex PCR Assay for Surveillance Isolates of Vancomycin-Resistant Enterococci. J. Clin. Microbiol. 38: 3092-3095 [Abstract] [Full Text]