Abstract
Whole-genome sequences for Stenotrophomonas maltophilia serial isolates from a bacteremic patient before and after development of levofloxacin resistance were assembled de novo and differed by one single-nucleotide variant in smeT, a repressor for multidrug efflux operon smeDEF. Along with sequenced isolates from five contemporaneous cases, they displayed considerable diversity compared against all published complete genomes. Whole-genome sequencing and complete assembly can conclusively identify resistance mechanisms emerging in S. maltophilia strains during clinical therapy.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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DNA, Bacterial / genetics
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Drug Resistance, Multiple, Bacterial / genetics
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Genome, Bacterial / genetics*
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Gram-Negative Bacterial Infections / microbiology*
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Microbial Sensitivity Tests
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Mutation
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Quinolones / pharmacology*
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Stenotrophomonas maltophilia / immunology*
Substances
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DNA, Bacterial
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Quinolones
Supplementary concepts
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Stenotrophomonas maltophilia bacteremia
Associated data
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GENBANK/CP011010
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GENBANK/CP011305
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GENBANK/CP011306
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GENBANK/JZIU00000000
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GENBANK/JZIU01000000
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GENBANK/JZIV00000000
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GENBANK/JZIV01000000
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GENBANK/JZIW00000000
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GENBANK/JZIW01000000
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GENBANK/JZTX00000000
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GENBANK/JZTX01000000