Multi-omics technologies applied to tuberculosis drug discovery

Aaron Goff, Daire Cantillon, Leticia Muraro Wildner, Simon J. Waddell

Research output: Contribution to journalReview articlepeer-review

29 Citations (Scopus)

Abstract

Multi-omics strategies are indispensable tools in the search for new anti-tuberculosis drugs. Omics methodologies, where the ensemble of a class of biological molecules are measured and evaluated together, enable drug discovery programs to answer two fundamental questions. Firstly, in a discovery biology approach, to find new targets in druggable pathways for target-based investigation, advancing from target to lead compound. Secondly, in a discovery chemistry approach, to identify the mode of action of lead compounds derived from high-throughput screens, progressing from compound to target. The advantage of multi-omics methodologies in both of these settings is that omics approaches are unsupervised and unbiased to a priori hypotheses, making omics useful tools to confirm drug action, reveal new insights into compound activity, and discover new avenues for inquiry. This review summarizes the application of Mycobacterium tuberculosis omics technologies to the early stages of tuberculosis antimicrobial drug discovery.
Original languageEnglish
Article number4629
JournalApplied Sciences (Switzerland)
Volume10
Issue number13
DOIs
Publication statusPublished - 1 Jul 2020
Externally publishedYes

Keywords

  • Antimicrobial drug resistance (AMR)
  • Drug discovery
  • Genomics
  • Lipidomics
  • Mechanism of action
  • Metabolomics
  • Mycobacterium
  • Proteomics
  • Target identification
  • Transcriptomics
  • Tuberculosis

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