Description du projet
Vers des traitements antifongiques innovants
Les infections fongiques humaines sont responsables de millions de décès chaque année, alors que les champignons peuvent également nuire aux plantes et aux cultures, générant d’importantes pertes en matière de production alimentaire. Malgré la disponibilité d’antifongiques et de fongicides, la résistance accrue aux médicaments met en exergue la nécessité de développer de nouveaux médicaments. Le but du projet FungiFeS, financé par l’UE, est d’identifier des composés naturels qui puissent servir de nouveaux antifongiques ou fongicides. Les chercheurs proposent comme nouvelles cibles les clusters fer-soufre (FeS) que l’on trouve dans les protéines impliquées dans des processus tels que la respiration cellulaire. Les résultats déboucheront sur de nouveaux traitements antifongiques combinatoires susceptibles d’améliorer la santé humaine et d’accroître la disponibilité d’aliments à l’échelle mondiale.
Objectif
Fungi have major socioeconomic impacts. Recent estimates suggest that invasive human fungal infections kill more than 1.6 million people annually and that 600 million people could be fed each year by halting the spread of fungal diseases in the five most important crops. A range of antifungals/fungicides is currently used to control fungal pathogens in medicine and agriculture, but resistance to those is growing underscoring the urgent need for new molecular targets and treatments. Iron-sulphur (FeS) clusters are inorganic cofactors found in all kingdoms of life and required for several essential cellular processes, such as DNA synthesis, mRNA translation, and respiration. Pathways required for their biogenesis were suggested to represent possible novel antifungal/fungicide targets. The aims of the project are: (1) to identify, via chemical high throughput screening, natural compounds targeting the essential mitochondrial (Arh1-Yah1) and cytoplasmic (Tah18-Dre2) NADPH-dependant electron transfer chains involved in the FeS cluster biogenesis. These compounds could be used in combination with other agents to kill fungal pathogens lowering cost and potential toxicity by reducing doses needed to inhibit fungal growth. (2) To highlight new targets for antifungals/fungicides among the FeS cluster biogenesis and associated pathways. (3) To establish the interaction network of the ferredoxin Yah1 involved in the early steps of the FeS cluster biogenesis knowing that several steps of this process remain poorly understood and new factors may still be discovered. The project will be carried out in the group “Oxidative stress, FeS protein and Cancer” (CNRS-ICSN, Gif-sur-Yvette, France) and will address those objectives by combining my own expertise and that of the host laboratory in microbiology, genetics, biophysics and biochemistry, drug screening and of cutting-edge technologies and approaches such as Förster resonance energy transfer, microfluidics and chemoproteomics.
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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)Coordinateur
75794 Paris
France