A bioluminescence-based chemical screen identifies a bactericidal naphthalene scaffold targeting MmpL3 in

Samsher Singh1, Ria Sorayah1, Yushu Chen2

  • 1Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 636921, Singapore.

Insights

Researchers discovered a new naphthalene-based drug effective against Mycobacterium abscessus pulmonary disease (Mabs-PD). This compound targets cell wall synthesis and respiration, showing potent bactericidal activity in preclinical models.

Area of Science:

  • Microbiology
  • Drug Discovery
  • Antimicrobial Resistance

Background:

  • Mycobacterium abscessus pulmonary disease (Mabs-PD) is a growing global health concern, especially for patients with cystic fibrosis or COPD.
  • Current treatments for Mabs-PD are limited by the lack of bactericidal antibiotics effective at therapeutic concentrations.
  • Targeting bacterial cell-wall synthesis is a promising strategy for developing new antimicrobials.

Purpose of the Study:

  • To develop and validate a bioluminescence-based assay for identifying bactericidal drugs against Mycobacterium abscessus.
  • To discover novel drug scaffolds targeting cell-wall synthesis and/or oxidative phosphorylation in M. abscessus.
  • To optimize lead compounds for potent activity against M. abscessus infections.

Main Methods:

  • Screening of a drug library using a novel bioluminescence-based whole-cell assay targeting cell-wall synthesis and oxidative phosphorylation.
  • Chemical optimization of identified hit compounds, focusing on a naphthalene scaffold.
  • Evaluation of lead compound efficacy in vitro (minimum inhibitory concentration, intracellular activity) and in vivo (zebrafish infection model).

Main Results:

  • The assay successfully identified known cell-wall targeting agents, validating its effectiveness.
  • A naphthalene scaffold was identified with potent bactericidal activity against M. abscessus.
  • The optimized derivative GM47-1 targets MmpL3, disrupts cell wall integrity, and affects respiration.
  • Further optimization yielded a derivative with nanomolar MIC, potent intracellular activity, and efficacy in a zebrafish model.

Conclusions:

  • A novel naphthalene scaffold provides a promising starting point for developing new therapeutics against Mabs-PD.
  • The developed bioluminescence assay is a valuable platform for rapid identification of bactericidal compounds against M. abscessus.
  • Targeting MmpL3 and respiration represents a viable strategy for combating M. abscessus infections.

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