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Mutations in the Esx-3 secretion system confer resistance to multiple chemical scaffolds in Mycobacterium tuberculosis

  • Theresa O’malley
  • , Matthew B. McNeil
  • , Devon Dennison
  • , Thomas Ioerger
  • , Tanya Parish
  • Infectious Disease Research Institute
  • Texas A&M University
  • TB Discovery Research
  • Seattle Biomedical Research Institute
  • University of Washington

Research output: Contribution to journalArticlepeer-review

Abstract

We determined the mechanism of resistance to seven chemical series with potent activity against Mycobacterium tuberculosis. Resistant mutants were isolated against the aminothiazoles, phenylhydrazones, 8-hydroxyquinolines, nitazoxanides, phenyl alkylimidazoles, morpholino thiophenes and trifluoromethyl pyrimidinones. We demonstrated that mutations in several components of the Esx-3 type VII secretion system (EccA3, EccB3, EccC3 and EccD3) conferred resistance to these disparate scaffolds. We conclude that mutations in Esx-3 are a common mechanism of resistance to anti-tubercular agents, which may have clinical relevance for new drugs.

Original languageEnglish
Article number001625
JournalMicrobiology (United Kingdom)
Volume171
Issue number11
DOIs
Publication statusPublished - 11 Nov 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • antibiotic resistance
  • metal ion homeostasis
  • mycobacteria
  • tuberculosis

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