Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides
ABSTRACT AFP is an antimicrobial peptide (AMP) produced by the filamentous fungus Aspergillus giganteus and is a very potent inhibitor of fungal growth that does not affect the viability of bacteria, plant, or mammalian cells. It targets chitin synthesis and causes plasma membrane permeabilization i...
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American Society for Microbiology
2019-12-01
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Series: | mSphere |
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Online Access: | https://journals.asm.org/doi/10.1128/mSphere.00741-19 |
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author | Norman Paege Dirk Warnecke Simone Zäuner Silke Hagen Ana Rodrigues Birgit Baumann Melanie Thiess Sascha Jung Vera Meyer |
author_facet | Norman Paege Dirk Warnecke Simone Zäuner Silke Hagen Ana Rodrigues Birgit Baumann Melanie Thiess Sascha Jung Vera Meyer |
author_sort | Norman Paege |
collection | DOAJ |
description | ABSTRACT AFP is an antimicrobial peptide (AMP) produced by the filamentous fungus Aspergillus giganteus and is a very potent inhibitor of fungal growth that does not affect the viability of bacteria, plant, or mammalian cells. It targets chitin synthesis and causes plasma membrane permeabilization in many human- and plant-pathogenic fungi, but its exact mode of action is not known. After adoption of the “damage-response framework of microbial pathogenesis” regarding the analysis of interactions between AMPs and microorganisms, we have recently proposed that the cytotoxic capacity of a given AMP depends not only on the presence/absence of its target(s) in the host and the AMP concentration applied but also on other variables, such as microbial survival strategies. We show here using the examples of three filamentous fungi (Aspergillus niger, Aspergillus fumigatus, and Fusarium graminearum) and two yeasts (Saccharomyces cerevisiae and Pichia pastoris) that the important parameters defining the AFP susceptibilities of these fungi are (i) the presence/absence of glycosylceramides, (ii) the presence/absence of Δ3(E) desaturation of the fatty acid chain therein, and (iii) the (dis)ability of these fungi to respond to AFP inhibitory effects with the fortification of their cell walls via increased chitin and β-(1,3)-glucan synthesis. These observations support the idea of the adoption of the damage-response framework to holistically understand the outcome of AFP inhibitory effects. IMPORTANCE Our data suggest a fundamental role of glycosylceramides in the susceptibility of fungi to AFP. We discovered that only a minor structural difference in these molecules—namely, the saturation level of their fatty acid chain, controlled by a 2-hydroxy fatty N-acyl-Δ3(E)-desaturase—represents a key to understanding the inhibitory activity of AFP. As glycosylceramides are important components of fungal plasma membranes, we propose a model which links AFP-mediated inhibition of chitin synthesis in fungi with its potential to disturb plasma membrane integrity. |
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language | English |
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spelling | doaj.art-5daaa7a311104ac281f9e46d9e7e3a5f2022-12-21T23:12:13ZengAmerican Society for MicrobiologymSphere2379-50422019-12-014610.1128/mSphere.00741-19Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of GlycosylceramidesNorman Paege0Dirk Warnecke1Simone Zäuner2Silke Hagen3Ana Rodrigues4Birgit Baumann5Melanie Thiess6Sascha Jung7Vera Meyer8Technische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyInstitute of Plant Science and Microbiology, University of Hamburg, Hamburg, GermanyInstitute of Plant Science and Microbiology, University of Hamburg, Hamburg, GermanyTechnische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyTechnische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyTechnische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyInstitute of Plant Science and Microbiology, University of Hamburg, Hamburg, GermanyTechnische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyTechnische Universität Berlin, Institute of Biotechnology, Chair of Applied and Molecular Microbiology, Berlin, GermanyABSTRACT AFP is an antimicrobial peptide (AMP) produced by the filamentous fungus Aspergillus giganteus and is a very potent inhibitor of fungal growth that does not affect the viability of bacteria, plant, or mammalian cells. It targets chitin synthesis and causes plasma membrane permeabilization in many human- and plant-pathogenic fungi, but its exact mode of action is not known. After adoption of the “damage-response framework of microbial pathogenesis” regarding the analysis of interactions between AMPs and microorganisms, we have recently proposed that the cytotoxic capacity of a given AMP depends not only on the presence/absence of its target(s) in the host and the AMP concentration applied but also on other variables, such as microbial survival strategies. We show here using the examples of three filamentous fungi (Aspergillus niger, Aspergillus fumigatus, and Fusarium graminearum) and two yeasts (Saccharomyces cerevisiae and Pichia pastoris) that the important parameters defining the AFP susceptibilities of these fungi are (i) the presence/absence of glycosylceramides, (ii) the presence/absence of Δ3(E) desaturation of the fatty acid chain therein, and (iii) the (dis)ability of these fungi to respond to AFP inhibitory effects with the fortification of their cell walls via increased chitin and β-(1,3)-glucan synthesis. These observations support the idea of the adoption of the damage-response framework to holistically understand the outcome of AFP inhibitory effects. IMPORTANCE Our data suggest a fundamental role of glycosylceramides in the susceptibility of fungi to AFP. We discovered that only a minor structural difference in these molecules—namely, the saturation level of their fatty acid chain, controlled by a 2-hydroxy fatty N-acyl-Δ3(E)-desaturase—represents a key to understanding the inhibitory activity of AFP. As glycosylceramides are important components of fungal plasma membranes, we propose a model which links AFP-mediated inhibition of chitin synthesis in fungi with its potential to disturb plasma membrane integrity.https://journals.asm.org/doi/10.1128/mSphere.00741-19antimicrobial peptideantifungal protein AFPgamma coredamage-response frameworksphingolipidglycosylceramide |
spellingShingle | Norman Paege Dirk Warnecke Simone Zäuner Silke Hagen Ana Rodrigues Birgit Baumann Melanie Thiess Sascha Jung Vera Meyer Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides mSphere antimicrobial peptide antifungal protein AFP gamma core damage-response framework sphingolipid glycosylceramide |
title | Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides |
title_full | Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides |
title_fullStr | Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides |
title_full_unstemmed | Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides |
title_short | Species-Specific Differences in the Susceptibility of Fungi to the Antifungal Protein AFP Depend on C-3 Saturation of Glycosylceramides |
title_sort | species specific differences in the susceptibility of fungi to the antifungal protein afp depend on c 3 saturation of glycosylceramides |
topic | antimicrobial peptide antifungal protein AFP gamma core damage-response framework sphingolipid glycosylceramide |
url | https://journals.asm.org/doi/10.1128/mSphere.00741-19 |
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