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Antimicrobial Agents and Chemotherapy, October 2000, p. 2679-2683, Vol. 44, No. 10
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Sequencing of the rpoB Gene in Legionella pneumophila and Characterization of Mutations Associated with Rifampin Resistance in the Legionellaceae

K. Nielsen,1 P. Hindersson,1 N. Høiby,1 and J. M. Bangsborg2,*

Department of Clinical Microbiology, Rigshospitalet, Copenhagen,1 and Department of Clinical Microbiology, Herlev Hospital, Herlev,2 Denmark

Received 8 November 1999/Returned for modification 19 March 2000/Accepted 1 July 2000

Rifampin in combination with erythromycin is a recommended treatment for severe cases of legionellosis. Mutations in the rpoB gene are known to cause rifampin resistance in Escherichia coli and Mycobacterium tuberculosis, and the purpose of the present study was to investigate a possible similar resistance mechanism within the members of the family Legionellaceae. Since the RNA polymerase genes of this genus have never been characterized, the DNA sequence of the Legionella pneumophila rpoB gene was determined by the Vectorette technique for genome walking. A 4,647-bp DNA sequence that contained the open reading frame (ORF) of the rpoB gene (4,104 bp) and an ORF of 384 bp representing part of the rpoC gene was obtained. A 316-bp DNA fragment in the center of the L. pneumophila rpoB gene, corresponding to a previously described site for mutations leading to rifampin resistance in M. tuberculosis, was sequenced from 18 rifampin-resistant Legionella isolates representing four species (L. bozemanii, L. longbeachae, L. micdadei, and L. pneumophila), and the sequences were compared to the sequences of the fragments from the parent (rifampin-sensitive) strains. Six single-base mutations which led to amino acid substitutions at five different positions were identified. A single strain did not contain any mutations in the 316-bp fragment. This study represents the characterization of a hitherto undescribed resistance mechanism within the family Legionellaceae.

* Corresponding author. Mailing address: Department of Clinical Microbiology 75K2, Herlev Hospital, Herlev Ringvej, DK-2730 Herlev, Denmark. Phone: 45 44 88 38 50. Fax: 45 44 88 37 72. E-mail: jeban{at}herlevhosp.kbhamt.dk.

Antimicrobial Agents and Chemotherapy, October 2000, p. 2679-2683, Vol. 44, No. 10
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.


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