4.7 Article

Whole-Genome Sequencing Identifies Emergence of a Quinolone Resistance Mutation in a Case of Stenotrophomonas maltophilia Bacteremia

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 59, Issue 11, Pages 7117-7120

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01723-15

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Funding

  1. Icahn Institute for Genomics and Multiscale Biology at Mount Sinai
  2. NIAID [5 T32 AI 7647-13]
  3. Department of Scientific Computing at the Icahn School of Medicine at Mount Sinai

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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.

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