Isoniazid resistance without a loss of fitness in Mycobacterium tuberculosis.

Jong-Hee Lee, Nicole C Ammerman, Scott Nolan, Deborah E Geiman, Shichun Lun, Haidan Guo, William R Bishai
Author Information
  1. Jong-Hee Lee: Center for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

Abstract

The emergence of multi- and extensively drug-resistant tuberculosis (MDR-TB and XDR-TB, respectively) has intensified the critical public health implications of this global disease. The fitness of Mycobacterium tuberculosis (M.TB.) strains exhibiting MDR and XDR phenotypes is of fundamental importance in predicting whether the MDR-/XDR-TB epidemic will be sustained across the human population. Here we describe a potential mechanism of M.TB. resistance to the TB drug Isoniazid (INH) conferred by loss of a sigma factor, SigI. We demonstrate that the gain of INH resistance in the M.TB. ΔsigI mutant might not diminish the organism's fitness for causing disease. These findings have significant implications when considering the ability of drug-resistant M.TB. strains to initiate untreatable TB epidemics, as it is possible that loss or alteration of SigI function could have a role in the generation of MDR and XDR M.TB. strains of suitable fitness to spread in a community setting.

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Grants

  1. AI036973/NIAID NIH HHS
  2. /Howard Hughes Medical Institute
  3. R01 AI079590/NIAID NIH HHS
  4. R01 AI037856/NIAID NIH HHS
  5. R01 AI036973/NIAID NIH HHS
  6. AI037856/NIAID NIH HHS
  7. AI079590/NIAID NIH HHS

MeSH Term

Animals
Antitubercular Agents
Bacterial Proteins
Catalase
Drug Resistance, Multiple, Bacterial
Genes, Bacterial
Genes, Regulator
Isoniazid
Macrophages
Mice
Mice, Inbred BALB C
Mycobacterium tuberculosis
Regulon
Sigma Factor
Transcription, Genetic
Tuberculosis
Tuberculosis, Multidrug-Resistant

Chemicals

Antitubercular Agents
Bacterial Proteins
Sigma Factor
Catalase
katG protein, Mycobacterium tuberculosis
Isoniazid

Word Cloud

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