Affiliation:
1. Department of Medical Genetics and Microbiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada
Abstract
ABSTRACT
Rifampin is a front-line antibiotic for the treatment of tuberculosis. Infections caused by rifampin- and multidrug-resistant
Mycobacterium tuberculosis
strains are difficult to treat and contribute to a poor clinical outcome. Rifampin resistance most often results from mutations in
rpoB
. However, some drug-resistant strains have
rpoB
alleles that encode the phenotype for susceptibility. Similarly, non-
M. tuberculosis
mycobacteria exhibit higher levels of baseline resistance to rifampin, despite the presence of
rpoB
alleles that encode the phenotype for susceptibility. To identify other genes involved in rifampin resistance, we generated a library of
Mycobacterium smegmatis
mc
2
155 transposon insertion mutants. Upon screening this library, we identified one mutant that was hypersensitive to rifampin. The transposon insertion was localized to the
arr
gene, which encodes rifampin ADP ribosyltransferase, an enzyme able to inactivate rifampin. Sequence analysis revealed differences in the
arr
alleles of
M. smegmatis
strain mc
2
155 and previously described strain DSM 43756. The
arr
region of strain mc
2
155 contains a second, partial copy of the
arr
gene plus a novel insertion sequence, IS
1623
.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
21 articles.
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