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Isoniazid Resistance in Mycobacterium tuberculosis Is a Heterogeneous Phenotype Composed of Overlapping MIC Distributions with Different Underlying Resistance Mechanisms.

Arash GhodousiElisa TaglianiEranga KarunaratneStefan NiemannJennifer PereraClaudio Umberto KöserDaniela Maria Cirillo
Published in: Antimicrobial agents and chemotherapy (2019)
MIC testing using the Bactec mycobacteria growth indicator tube system 960 of 70 phylogenetically diverse, isoniazid-resistant clinical strains of Mycobacterium tuberculosis revealed a complex pattern of overlapping MIC distributions. Whole-genome sequencing explained most of the levels of resistance observed. The MIC distribution of strains with only inhA promoter mutations was split by the current concentration endorsed by the Clinical and Laboratory Standards Institute to detect low-level resistance to isoniazid and is, consequently, likely not optimally set.
Keyphrases
  • mycobacterium tuberculosis
  • pulmonary tuberculosis
  • escherichia coli
  • gene expression
  • dna methylation
  • transcription factor