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Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa

The membrane sphingolipid glucosylceramide (GlcCer) plays an important role in fungal fitness and adaptation to most diverse environments. Moreover, reported differences in the structure of GlcCer between fungi, plants and animals render this pathway a promising target for new generation therapeutic...

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Autores principales: Huber, Anna, Oemer, Gregor, Malanovic, Nermina, Lohner, Karl, Kovács, Laura, Salvenmoser, Willi, Zschocke, Johannes, Keller, Markus A., Marx, Florentine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471014/
https://www.ncbi.nlm.nih.gov/pubmed/31031714
http://dx.doi.org/10.3389/fmicb.2019.00605
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author Huber, Anna
Oemer, Gregor
Malanovic, Nermina
Lohner, Karl
Kovács, Laura
Salvenmoser, Willi
Zschocke, Johannes
Keller, Markus A.
Marx, Florentine
author_facet Huber, Anna
Oemer, Gregor
Malanovic, Nermina
Lohner, Karl
Kovács, Laura
Salvenmoser, Willi
Zschocke, Johannes
Keller, Markus A.
Marx, Florentine
author_sort Huber, Anna
collection PubMed
description The membrane sphingolipid glucosylceramide (GlcCer) plays an important role in fungal fitness and adaptation to most diverse environments. Moreover, reported differences in the structure of GlcCer between fungi, plants and animals render this pathway a promising target for new generation therapeutics. Our knowledge about the GlcCer biosynthesis in fungi is mainly based on investigations of yeasts, whereas this pathway is less well characterized in molds. We therefore performed a detailed lipidomic profiling of GlcCer species present in Neurospora crassa and comprehensively show that the deletion of genes encoding enzymes involved in GlcCer biosynthesis affects growth, conidiation and stress response in this model fungus. Importantly, our study evidences that differences in the pathway intermediates and their functional role exist between N. crassa and other fungal species. We further investigated the role of GlcCer in the susceptibility of N. crassa toward two small cysteine-rich and cationic antimicrobial proteins (AMPs), PAF and PAFB, which originate from the filamentous ascomycete Penicillium chrysogenum. The interaction of these AMPs with the fungal plasma membrane is crucial for their antifungal toxicity. We found that GlcCer determines the susceptibility of N. crassa toward PAF, but not PAFB. A higher electrostatic affinity of PAFB than PAF to anionic membrane surfaces might explain the difference in their antifungal mode of action.
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spelling pubmed-64710142019-04-26 Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa Huber, Anna Oemer, Gregor Malanovic, Nermina Lohner, Karl Kovács, Laura Salvenmoser, Willi Zschocke, Johannes Keller, Markus A. Marx, Florentine Front Microbiol Microbiology The membrane sphingolipid glucosylceramide (GlcCer) plays an important role in fungal fitness and adaptation to most diverse environments. Moreover, reported differences in the structure of GlcCer between fungi, plants and animals render this pathway a promising target for new generation therapeutics. Our knowledge about the GlcCer biosynthesis in fungi is mainly based on investigations of yeasts, whereas this pathway is less well characterized in molds. We therefore performed a detailed lipidomic profiling of GlcCer species present in Neurospora crassa and comprehensively show that the deletion of genes encoding enzymes involved in GlcCer biosynthesis affects growth, conidiation and stress response in this model fungus. Importantly, our study evidences that differences in the pathway intermediates and their functional role exist between N. crassa and other fungal species. We further investigated the role of GlcCer in the susceptibility of N. crassa toward two small cysteine-rich and cationic antimicrobial proteins (AMPs), PAF and PAFB, which originate from the filamentous ascomycete Penicillium chrysogenum. The interaction of these AMPs with the fungal plasma membrane is crucial for their antifungal toxicity. We found that GlcCer determines the susceptibility of N. crassa toward PAF, but not PAFB. A higher electrostatic affinity of PAFB than PAF to anionic membrane surfaces might explain the difference in their antifungal mode of action. Frontiers Media S.A. 2019-04-11 /pmc/articles/PMC6471014/ /pubmed/31031714 http://dx.doi.org/10.3389/fmicb.2019.00605 Text en Copyright © 2019 Huber, Oemer, Malanovic, Lohner, Kovács, Salvenmoser, Zschocke, Keller and Marx. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Huber, Anna
Oemer, Gregor
Malanovic, Nermina
Lohner, Karl
Kovács, Laura
Salvenmoser, Willi
Zschocke, Johannes
Keller, Markus A.
Marx, Florentine
Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title_full Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title_fullStr Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title_full_unstemmed Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title_short Membrane Sphingolipids Regulate the Fitness and Antifungal Protein Susceptibility of Neurospora crassa
title_sort membrane sphingolipids regulate the fitness and antifungal protein susceptibility of neurospora crassa
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471014/
https://www.ncbi.nlm.nih.gov/pubmed/31031714
http://dx.doi.org/10.3389/fmicb.2019.00605
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