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Microbial Drug Resistance
Detection of Mutations Associated with Macrolide Resistance in Thermophilic Campylobacter spp. by Real-Time PCR
To cite this article:
Sylvie Vacher, Armelle Menard, Elisabeth Bernard, Adriana Santos, Francis Megraud.
Microbial Drug Resistance.
Spring 2005,
11(1): 40-47.
doi:10.1089/mdr.2005.11.40.
Sylvie Vacher Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hôpital Pellegrin, Bordeaux, France; and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France. Dr. Armelle Menard Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hôpital Pellegrin, Bordeaux, France; and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France. Elisabeth Bernard Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hôpital Pellegrin, Bordeaux, France; and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France. Adriana Santos Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hôpital Pellegrin, Bordeaux, France; and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France. Francis Megraud Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hôpital Pellegrin, Bordeaux, France; and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France. Two point mutations (A2074C and A2075G) in the 23S rRNA gene of Campylobacter coli and C. jejuni are associated with erythromycin resistance. A real-time fluorescence resonance energy transfer PCR assay using a melting curve analysis was developed to identify these two point mutations and the wild-type genotype in thermophilic Campylobacter species such as C. coli, C. jejuni, and C. lari. Concerning these species, 141 strains were tested and a result obtained in 140 (99.3%). A single genotype was detected in 133 cases and two genotypes in seven cases. There was an agreement with the phenotypic methods except for one C. coli strain that was not amplified during the PCR assay. The A2075G mutation was mainly found among the 92 resistant strains tested (95.6%) and the A2074C mutation only twice (2.2%). One C. jejuni strain (1.1%) harbored both mutations on the same 23S rDNA copy. When compared to the phenotypic tests, the new real-time PCR assay was able to detect the correct genotype, in all cases except one (1.1%). This assay is more sensitive and more rapid than other PCR assays, the entire procedure taking less than 2 hr.  This paper was cited by:Inaccuracy of routine susceptibility tests for detection of erythromycin resistance of
Campylobacter jejuni
and
Campylobacter coli M. T. van der Beek, E. C. J. Claas, D. J. Mevius, W. van Pelt, J. A. Wagenaar, E. J. Kuijper Clinical Microbiology and Infection. Jun 2009 CrossRef 23S rRNA Gene Mutations Contributing to Macrolide Resistance in Campylobacter jejuni and Campylobacter coli Scott R. Ladely, Richard J. Meinersmann, Mark D. Englen, Paula J. Fedorka-Cray, Mark A. Harrison Foodborne Pathogens and Disease. Feb 2009, Vol. 6, No. 1: 91-98 Abstract | Full Text PDF | Reprints & PermissionsAntibiotic resistance and resistance mechanisms in Campylobacter jejuni and Campylobacter coli David A. Alfredson, Victoria Korolik FEMS Microbiology Letters. Jan 2008, Vol. 277, No. 2: 123-132 CrossRef Prevalence and antimicrobial resistance of Campylobacter in US dairy cattle M.D. Englen, A.E. Hill, D.A. Dargatz, S.R. Ladely, P.J. Fedorka-Cray Journal of Applied Microbiology. Jul 2007, Vol. 102, No. 6: 1570-1577 CrossRef
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