Contribution ofrpoB2RNA Polymerase β Subunit Gene to Rifampin Resistance inNocardiaSpecies
- 1 April 2006
- journal article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 50 (4), 1342-6
- https://doi.org/10.1128/aac.50.4.1342-1346.2006
Abstract
Nocardia species are gram-positive environmental saprophytes, but some cause the infectious disease nocardiosis. The complete genomic sequence of Nocardia farcinica IFM 10152 has been determined, and analyses indicated the presence of two different RNA polymerase beta subunit genes, rpoB and rpoB2, in the genome (J. Ishikawa, A. Yamashita, Y. Mikami, Y. Hoshino, H. Kurita, K. Hotta, T. Shiba, and M. Hattori, Proc. Natl. Acad. Sci. USA 101:14925-14930, 2004). These genes share 88.8% identity at the nucleotide level. Moreover, comparison of their amino acid sequences with those of other bacterial RpoB proteins suggested that the nocardial RpoB protein is likely to be rifampin (RIF) sensitive, whereas RpoB2 protein contains substitutions at the RIF-binding region that are likely to confer RIF resistance. Southern analysis indicated that rpoB duplication is widespread in Nocardia species and is correlated with the RIF-resistant phenotype. The introduction of rpoB2 by using a newly developed Nocardia-Escherichia coli shuttle plasmid vector and transformation system conferred RIF resistance to Nocardia asteroides IFM 0319T, which has neither RIF resistance nor rpoB duplication. Furthermore, unmarked rpoB2 deletion mutants of N. farcinica IFM 10152 showed no significant resistance to RIF. These results indicated the contribution of rpoB2 to RIF resistance in Nocardia species. Since this is the first example of genetic engineering of the Nocardia genome, we believe that this study, as well as our determination of the N. farcinica genome sequence, will be a landmark in Nocardia genetics.Keywords
This publication has 26 references indexed in Scilit:
- Distribution of Nocardia Species in Clinical Samples and Their Routine Rapid Identification in the LaboratoryJournal of Clinical Microbiology, 2005
- Natural merodiploidy involving duplicated rpoB alleles affects secondary metabolism in a producer actinomyceteMolecular Microbiology, 2004
- Effect of rpoB Mutations Conferring Rifampin Resistance on Fitness of Mycobacterium tuberculosisAntimicrobial Agents and Chemotherapy, 2004
- RNA Polymerase Mutation Activates the Production of a Dormant Antibiotic 3,3′-Neotrehalosadiamine via an Autoinduction Mechanism in Bacillus subtilisJournal of Biological Chemistry, 2004
- Activation of Antibiotic Biosynthesis by Specified Mutations in the rpoB Gene (Encoding the RNA Polymerase β Subunit) of Streptomyces lividansJournal of Bacteriology, 2002
- Colony PCR for Detection of Specific DNA Sequences in Actinomycetes.Actinomycetologica, 2000
- Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicumGene, 1994
- Phosphorylative inactivation of rifampicin by Nocardia otitidiscaviarumJournal of Antimicrobial Chemotherapy, 1994
- Actinomycete infections in humans — a reviewGene, 1992
- Isolation and characterization of efficient plasmid transformation mutants of Mycobacterium smegmatisMolecular Microbiology, 1990