Mycobacterium tuberculosis virulence inhibitors discovered by Mycobacterium marinum high-throughput screening.
Hasan TükenmezIsabel EdströmRamesh UmmanniStina Berglund FickCharlotta SundinMikael ElofssonChrister LarssonPublished in: Scientific reports (2019)
High-throughput screening facilities do not generally support biosafety level 3 organisms such as Mycobacterium tuberculosis. To discover not only antibacterials, but also virulence inhibitors with either bacterial or host cell targets, an assay monitoring lung fibroblast survival upon infection was developed and optimized for 384-plate format and robotic liquid handling. By using Mycobacterium marinum as surrogate organism, 28,000 compounds were screened at biosafety level 2 classification, resulting in 49 primary hits. Exclusion of substances with unfavourable properties and known antimicrobials resulted in 11 validated hits of which 7 had virulence inhibiting properties and one had bactericidal effect also in wild type Mycobacterium tuberculosis. This strategy to discover virulence inhibitors using a model organism in high-throughput screening can be a valuable tool for other researchers working on drug discovery against tuberculosis and other biosafety level 3 infectious agents.
Keyphrases
- mycobacterium tuberculosis
- pseudomonas aeruginosa
- escherichia coli
- staphylococcus aureus
- antimicrobial resistance
- biofilm formation
- drug discovery
- pulmonary tuberculosis
- wild type
- machine learning
- deep learning
- signaling pathway
- cystic fibrosis
- drinking water
- single cell
- cell therapy
- emergency department
- mesenchymal stem cells
- multidrug resistant
- human immunodeficiency virus
- wound healing