Biometals and Drug Discovery Lab

Biometals

The importance of metals for the survival of microorganisms is best demonstrated on iron. Phytoplankton contributes to nearly 50% of the primary production, yet waters of the oceans contain limiting concentrations of several essential nutrients, especially iron, an element that is required in particular abundance by photosynthetic organisms. Iron also plays an important role in host-pathogen relationship. Many pathogens are highly dependent on a sufficient supply of iron and take up this metal by multiple and divergent pathways from the host. The activation and expression of such microbial iron acquisition systems is linked to their pathogenicity and proliferation. Thus the withholding of iron is an effective antimicrobial defence strategy of the host. Our project is focused on the characterization of nutrition requirements, mechanism of uptake and intracellular metabolism of metals, mainly iron and copper and identification of molecules involved in these processes. Research includes metabolism specific for pathogenic organisms (parasitic protists) and strategies necessary for life in nutritionally limited environment (unicellular algae). As a model organism we are using Saccharomyces cerevisiae.

Iron sources available to marine phytoplankton and employed uptake pathways.

Robert Sutak et al. Front. Microbiol. 2020, 11:566691

© 2020 Sutak, Camadro and Lesuisse.


Representation of iron transport systems in parasitic protists.

Jan Mach & Robert Sutak. Metallomics 2020,12, 1335-1347

© The Royal Society of Chemistry 2020

Drug discovery

Many of the currently available anti-parasitic and anti-fungal frontline drugs have severe limitations, including adverse side effects, complex administration, and increasing occurrence of resistance. Our laboratory is involved in discovering new and repurposing drugs against medically important pathogenic eukaryotic microorganisms such as the causative agents of sleeping sickness, Chagas disease, malaria, the pathogenic yeasts Candida albicans and Cryptococcus neoformans, the brain-eating amoeba Naegleria fowleri, and the causative agent of acanthamoebic keratitis. For in vivo studies, we use mouse models of Cryptococcus neoformans and Trypanosoma brucei infection. An example of successful drug repurposing is the potential use of the anticancer drug MitoTam as a highly selective antiparasitic.

Repurposing of MitoTam: Novel Anti-Cancer Drug Candidate Exhibits Potent Activity against Major Protozoan and Fungal Pathogens.

Arbon et al. Antimicrob Agents Chemother. 2022

© 2022 Arbon et al.

Schematic representation of the proposed MitoTam mode of action on T. brucei mitochondrion