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Clinical Chemistry 52: 2294-2296, 2006. First published October 19, 2006; 10.1373/clinchem.2006.075309
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(Clinical Chemistry. 2006;52:2294-2296.)
© 2006 American Association for Clinical Chemistry, Inc.


Technical Briefs

A Novel Real-Time Duplex PCR Assay for Detecting penA and ponA Genotypes in Neisseria gonorrhoeae: Comparison with Phenotypes Determined by the E-Test

Frédérique Vernel-Pauillac and Fabrice Meriena

Laboratoire de Recherche en Bactériologie, Institut Pasteur de Nouvelle-Calédonie, Nouvelle-Calédonie

aAddress correspondence to this author at: Institut Pasteur of New Caledonia, BP 61 98845 Noumea cedex, New Caledonia. Fax 00-687-27-33-90; e-mail fmerien{at}pasteur.nc


Abstract

Background: For many years, the pathogenic bacterium Neisseria gonorrhoeae, the etiologic agent of gonorrhea, was generally susceptible to penicillin, until the emergence of resistant strains. Well-characterized genetic variations in the penicillin resistance–determining region correlate with decreased susceptibility to penicillin. At least 5 genes (penA, penB, mtrR, ponA, and penC) are involved in the chromosomally mediated resistance to this antibiotic. To date, no development of multiplex PCR assays targeting a range of gonococcal genes and variations as a means of predicting antibiotic resistance has been reported.

Methods: The aim of this study was to develop a duplex assay using DNA from isolated strains. We describe the development and evaluation on the LightCycler platform of a real-time duplex PCR assay (hybridization probe format) for rapid and specific detection of ponA and penA variations, predicting penicillin susceptibilities.

Results: The real-time duplex PCR assay successfully detected variations in ponA and penA genes by use of distinct melting temperatures from a total of 120 Neisseria gonorrhoeae isolates. Moreover, the variation profiles obtained with the real-time PCR and the melting analysis showed good correlation with the pattern of penicillin susceptibility generated with classical antibiograms. Nucleotide sequencing data were in complete agreement with multiplex assay results.

Conclusions: The presented assay is suitable for the detection of chromosomally mediated resistant strains of Neisseria gonorrhoeae in genotyping studies and could be valuable in the effective antimicrobial strategy to gonococci.




The following articles in journals at HighWire Press have cited this article:


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Antimicrob. Agents Chemother.Home page
F. Vernel-Pauillac, S. Nandi, R. A. Nicholas, and C. Goarant
Genotyping as a Tool for Antibiotic Resistance Surveillance of Neisseria gonorrhoeae in New Caledonia: Evidence of a Novel Genotype Associated with Reduced Penicillin Susceptibility
Antimicrob. Agents Chemother., September 1, 2008; 52(9): 3293 - 3300.
[Abstract] [Full Text] [PDF]




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