Tomatidine Is a Lead Antibiotic Molecule That Targets Staphylococcus aureus ATP Synthase Subunit C

• Published in: Antimicrobial agents and chemotherapy Vol. 62; no. 6
• Main Authors: Lamontagne Boulet, Maxime, Isabelle, Charles, Guay, Isabelle, Brouillette, Eric, Langlois, Jean-Philippe, Jacques, Pierre-Étienne, Rodrigue, Sébastien, Brzezinski, Ryszard, Beauregard, Pascale B, Bouarab, Kamal, Boyapelly, Kumaraswamy, Boudreault, Pierre-Luc, Marsault, Éric, Malouin, François
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01-06-2018
• Subjects: Anti-Bacterial Agents; Experimental Therapeutics; Mitochondrial Proton-Translocating ATPases; Staphylococcus aureus; Tomatine; tomatidine; new target; small-colony variant; ATP synthase; Staphylococcus aureus
• ISSN: 0066-4804; 1098-6596
• DOI: 10.1128/AAC.02197-17

Methicillin-resistant
(MRSA) is a leading cause of deadly hospital-acquired infections. The discovery of anti-
antibiotics and new classes of drugs not susceptible to the mechanisms of resistance shared among bacteria is imperative. We recently showed that tomatidine (TO), a steroidal alkaloid from solanaceous plants, possesses potent antibacterial activity against
small-colony variants (SCVs), the notoriously persistent form of this bacterium that has been associated with recurrence of infections. Here, using genomic analysis of
-generated TO-resistant
strains to identify mutations in genes involved in resistance, we identified the bacterial ATP synthase as the cellular target. Sequence alignments were performed to highlight the modified sequences, and the structural consequences of the mutations were evaluated in structural models. Overexpression of the
gene in
SCVs or introducing the mutation found in the
gene of one of the high-level TO-resistant
mutants into the
gene provided resistance to TO and further validated the identity of the cellular target. FC04-100, a TO derivative which also possesses activity against non-SCV strains, prevents high-level resistance development in prototypic strains and limits the level of resistance observed in SCVs. An ATP synthesis assay allowed the observation of a correlation between antibiotic potency and ATP synthase inhibition. The selectivity index (inhibition of ATP production by mitochondria versus that of bacterial ATP synthase) is estimated to be >10
-fold for FC04-100.