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High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines
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-resist...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147771/ https://www.ncbi.nlm.nih.gov/pubmed/27855158 http://dx.doi.org/10.1371/journal.pgen.1006374 |
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author | Filipuzzi, Ireos Cotesta, Simona Perruccio, Francesca Knapp, Britta Fu, Yue Studer, Christian Pries, Verena Riedl, Ralph Helliwell, Stephen B. Petrovic, Katarina T. Movva, N. Rao Sanglard, Dominique Tao, Jianshi Hoepfner, Dominic |
author_facet | Filipuzzi, Ireos Cotesta, Simona Perruccio, Francesca Knapp, Britta Fu, Yue Studer, Christian Pries, Verena Riedl, Ralph Helliwell, Stephen B. Petrovic, Katarina T. Movva, N. Rao Sanglard, Dominique Tao, Jianshi Hoepfner, Dominic |
author_sort | Filipuzzi, Ireos |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5147771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51477712016-12-21 High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines Filipuzzi, Ireos Cotesta, Simona Perruccio, Francesca Knapp, Britta Fu, Yue Studer, Christian Pries, Verena Riedl, Ralph Helliwell, Stephen B. Petrovic, Katarina T. Movva, N. Rao Sanglard, Dominique Tao, Jianshi Hoepfner, Dominic PLoS Genet Research Article 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. Public Library of Science 2016-11-17 /pmc/articles/PMC5147771/ /pubmed/27855158 http://dx.doi.org/10.1371/journal.pgen.1006374 Text en © 2016 Filipuzzi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Filipuzzi, Ireos Cotesta, Simona Perruccio, Francesca Knapp, Britta Fu, Yue Studer, Christian Pries, Verena Riedl, Ralph Helliwell, Stephen B. Petrovic, Katarina T. Movva, N. Rao Sanglard, Dominique Tao, Jianshi Hoepfner, Dominic High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title | High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title_full | High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title_fullStr | High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title_full_unstemmed | High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title_short | High-Resolution Genetics Identifies the Lipid Transfer Protein Sec14p as Target for Antifungal Ergolines |
title_sort | high-resolution genetics identifies the lipid transfer protein sec14p as target for antifungal ergolines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147771/ https://www.ncbi.nlm.nih.gov/pubmed/27855158 http://dx.doi.org/10.1371/journal.pgen.1006374 |
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