Invasive infections by fungal pathogens cause more deaths than malaria worldwide. We found the ergoline compound NGx04 in an antifungal screen, with selectivity over mammalian cells. High-resolution chemogenomics identified the lipid transfer protein Sec14p as the target of NGx04 and compound-resistant mutations in Sec14p define compound-target interactions in the substrate binding pocket of the protein. Beyond its essential lipid transfer function in a variety of pathogenic fungi, Sec14p is also involved in secretion of virulence determinants essential for the pathogenicity of fungi such as Cryptococcus neoformans , making Sec14p an attractive antifungal target. Consistent with this dual function, we demonstrate that NGx04 inhibits the growth of two clinical isolates of C . neoformans and that NGx04-related compounds have equal and even higher potency against C . neoformans . Furthermore NGx04 analogues showed fungicidal activity against a fluconazole resistant C . neoformans strain. In summary, we present genetic evidence that NGx04 inhibits fungal Sec14p and initial data supporting NGx04 as a novel antifungal starting point. Author Summary Emerging resistance to antibiotics led to an inglorious revival of infectious diseases. Furthermore, in the past 30 years, only one novel anti-fungal target has been discovered which was used to develop therapies against. Therefore pathogen-selective targets and knowledge about possible resistance determinants are of utmost importance to successfully develop new medicines. Here we describe the identification of anti-fungal ergolines, targeting the lipid transfer protein Sec14p, and inhibiting the growth of two clinical isolates of the pathogenic fungus Cryptococcus neoformans . Both, compound and target represent attractive points for further investigations: Sec14p as it differs significantly from the human homolog and as it has been implicated in fungal viability and pathogenicity, and, ergolines as they are used in the clinic against a variety of diseases demonstrating both efficacy and safety.
【초록키워드】 therapy, Mutation, Infectious diseases, Diseases, knowledge, Genetic, Infection, Antibiotics, malaria, Protein, viability, death, target, Pathogens, Efficacy and safety, selectivity, pathogenicity, analogues, virulence, fungi, disease, fungal, Evidence, Interaction, dual, Cryptococcus neoformans, fluconazole, starting point, resistance to antibiotics, determinant, Medicines, growth, secretion, Compound, clinic, genetic evidence, transfer, binding pocket, pathogenic, fungicidal activity, fungal pathogens, mammalian cells, homolog, ergoline, ergolines, analogue, isolate, initial, was used, develop, significantly, involved, inhibit, variety, inhibiting, implicated, Cryptococcus neoforman, fungal pathogen, 【제목키워드】 Antifungal, Lipid,