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Antimicrobial Agents and Chemotherapy, March 2003, p. 1125-1128, Vol. 47, No. 3
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.3.1125-1128.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
PCR-Restriction Fragment Length Polymorphism Analysis for Detection of Point Mutations Associated with Macrolide Resistance in Campylobacter spp.
Sylvie Vacher, Armelle Ménard,* Elisabeth Bernard, and Francis Mégraud
Centre National de Référence des Helicobacters et Campylobacters, Laboratoire de Bactériologie, Hopital Pellegrin, and Laboratoire de Bactériologie, Université Victor Segalen Bordeaux 2, Bordeaux, France
Received 13 September 2002/
Returned for modification 25 November 2002/
Accepted 20 December 2002
A 23S rRNA gene fragment in domain V was sequenced from 30 clinical isolates of Campylobacter spp., including 22 resistant to macrolides. Two point mutations associated with erythromycin resistance were identified at positions 2074 and 2075 on the 23S rRNA gene (homologous to A2142C and A2143G mutations in Helicobacter pylori) in which an adenine residue is also replaced with a cytosine and a guanine residue, respectively. A combined PCR-restriction fragment length polymorphism technique was developed to detect these mutations by using the BsaI and BceAI enzymes.
* Corresponding author. Mailing address: Laboratoire de Bactériologie, Zone Nord, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France. Phone: 33 5-57-57-12-88. Fax: 33 5-56-79-60-18. E-mail:
armelle.menard{at}labhel.u-bordeaux2.fr.
Antimicrobial Agents and Chemotherapy, March 2003, p. 1125-1128, Vol. 47, No. 3
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.3.1125-1128.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
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