Abstract
We examined the molecular mechanisms of resistance to kanamycin and viomycin in Mycobacterium smegmatis. All of the M. smegmatis strains with high-level kanamycin resistance had a nucleotide substitution from A to G at position 1389 of the 16S rRNA gene (rrs). This position is equivalent to position 1408 of Escherichia coli, and mutation at this position is known to cause aminoglycoside resistance. Mutations from G to A or G to T at position 1473 of the M. smegmatis rrs gene were found in viomycin-resistant mutants which had been designated vicB mutants in our earlier studies. Using the M. smegmatis conjugation system, we confirmed that these mutations indeed contributed to kanamycin and viomycin resistance, and kanamycin susceptibility was dominant over resistance in a heterogenomic strain. Additional experiments showed that three of four Mycobacterium tuberculosis strains with high-level kanamycin resistance had a mutation from A to G at position 1400, which was equivalent to position 1389 of M. smegmatis.
MeSH Terms
Base Sequence
Capreomycin/pharmacology
Conjugation, Genetic
DNA, Bacterial
Drug Resistance, Microbial/genetics
Drug Resistance, Multiple/genetics
Genes, Dominant
Genes, Recessive
Genome, Bacterial
Kanamycin Resistance/genetics
Molecular Sequence Data
Mutation
Mycobacterium/drug effects,genetics
Mycobacterium tuberculosis/genetics,isolation & purification
RNA, Bacterial
RNA, Ribosomal, 16S
Sequence Analysis, RNA
Viomycin/pharmacology
Chemicals
DNA, Bacterial
RNA, Bacterial
RNA, Ribosomal, 16S
Capreomycin
Viomycin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Taniguchi H
Department of Microbiology, School of Medicine, University of Occupational and Environmental Health, Yahatanishiku, Kitakyusyu, Japan. hatsumi@med.uoeh-u.ac.jp
Chang B
Abe C
Nikaido Y
Mizuguchi Y
Yoshida S I
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