The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection

ABSTRACT Fusarium verticillioides produces the mycotoxin fumonisin B1 (FB1), which disrupts sphingolipid biosynthesis by inhibiting ceramide synthase and affects the health of plants, animals, and humans. The means by which F. verticillioides protects itself from its own mycotoxin are not completely...

Full description

Saved in:
Bibliographic Details
Main Authors: Fabio Gherlone, Katarina Jojić, Ying Huang, Sandra Hoefgen, Vito Valiante, Slavica Janevska
Format: Article
Language:English
Published: American Society for Microbiology 2025-02-01
Series:mBio
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mbio.02681-24
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832096526990573568
author Fabio Gherlone
Katarina Jojić
Ying Huang
Sandra Hoefgen
Vito Valiante
Slavica Janevska
author_facet Fabio Gherlone
Katarina Jojić
Ying Huang
Sandra Hoefgen
Vito Valiante
Slavica Janevska
author_sort Fabio Gherlone
collection DOAJ
description ABSTRACT Fusarium verticillioides produces the mycotoxin fumonisin B1 (FB1), which disrupts sphingolipid biosynthesis by inhibiting ceramide synthase and affects the health of plants, animals, and humans. The means by which F. verticillioides protects itself from its own mycotoxin are not completely understood. Some fumonisin (FUM) cluster genes do not contribute to the biosynthesis of the compound, but their function has remained enigmatic. Recently, we showed that FUM17, FUM18, and FUM19 encode two ceramide synthases and an ATP-binding cassette transporter, respectively, which play a role in antagonizing the toxicity mediated by FB1. In the present work, we uncovered functions of two adjacent genes, FUM15 and FUM16. Using homologous and heterologous expression systems, in F. verticillioides and Saccharomyces cerevisiae, respectively, we provide evidence that both contribute to protection against FB1. Our data indicate a potential role for the P450 monooxygenase Fum15 in the modification and detoxification of FB1 since the deletion and overexpression of the respective gene affected extracellular FB1 levels in both hosts. Furthermore, relative quantification of ceramide intermediates and an in vitro enzyme assay revealed that Fum16 is a functional palmitoyl-CoA ligase. It co-localizes together with the ceramide synthase Fum18 to the endoplasmic reticulum, where they contribute to sphingolipid biosynthesis. Thereby, FUM15-19 constitute a subcluster within the FUM biosynthetic gene cluster dedicated to the fungal self-protection against FB1.IMPORTANCEThe study identifies a five-gene FUM subcluster (FUM15-19) in Fusarium verticillioides involved in self-protection against FB1. FUM16 (palmitoyl-CoA ligase), FUM17, and FUM18 (ceramide synthases) enzymatically supplement ceramide biosynthesis, while FUM19 (ATP-binding cassette transporter) acts as a repressor of the FUM cluster. The evolutionary conservation of FUM15 (P450 monooxygenase) in Fusarium and Aspergillus FUM clusters is discussed, and its effect on extracellular FB1 levels in both native (F. verticillioides) and heterologous (Saccharomyces cerevisiae) hosts is highlighted. These findings enhance our understanding of mycotoxin self-protection mechanisms and could inform strategies for predicting biological activity of unknown secondary metabolites, managing mycotoxin contamination, and developing resistant crop cultivars.
format Article
id doaj-art-9226633084824aa4a02eaedd50f1c5c4
institution Kabale University
issn 2150-7511
language English
publishDate 2025-02-01
publisher American Society for Microbiology
record_format Article
series mBio
spelling doaj-art-9226633084824aa4a02eaedd50f1c5c42025-02-05T14:00:48ZengAmerican Society for MicrobiologymBio2150-75112025-02-0116210.1128/mbio.02681-24The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protectionFabio Gherlone0Katarina Jojić1Ying Huang2Sandra Hoefgen3Vito Valiante4Slavica Janevska5(Epi-)Genetic Regulation of Fungal Virulence, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, GermanyBiobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, GermanyBiobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, GermanyBiobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, GermanyBiobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, Germany(Epi-)Genetic Regulation of Fungal Virulence, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute (Leibniz-HKI), Jena, GermanyABSTRACT Fusarium verticillioides produces the mycotoxin fumonisin B1 (FB1), which disrupts sphingolipid biosynthesis by inhibiting ceramide synthase and affects the health of plants, animals, and humans. The means by which F. verticillioides protects itself from its own mycotoxin are not completely understood. Some fumonisin (FUM) cluster genes do not contribute to the biosynthesis of the compound, but their function has remained enigmatic. Recently, we showed that FUM17, FUM18, and FUM19 encode two ceramide synthases and an ATP-binding cassette transporter, respectively, which play a role in antagonizing the toxicity mediated by FB1. In the present work, we uncovered functions of two adjacent genes, FUM15 and FUM16. Using homologous and heterologous expression systems, in F. verticillioides and Saccharomyces cerevisiae, respectively, we provide evidence that both contribute to protection against FB1. Our data indicate a potential role for the P450 monooxygenase Fum15 in the modification and detoxification of FB1 since the deletion and overexpression of the respective gene affected extracellular FB1 levels in both hosts. Furthermore, relative quantification of ceramide intermediates and an in vitro enzyme assay revealed that Fum16 is a functional palmitoyl-CoA ligase. It co-localizes together with the ceramide synthase Fum18 to the endoplasmic reticulum, where they contribute to sphingolipid biosynthesis. Thereby, FUM15-19 constitute a subcluster within the FUM biosynthetic gene cluster dedicated to the fungal self-protection against FB1.IMPORTANCEThe study identifies a five-gene FUM subcluster (FUM15-19) in Fusarium verticillioides involved in self-protection against FB1. FUM16 (palmitoyl-CoA ligase), FUM17, and FUM18 (ceramide synthases) enzymatically supplement ceramide biosynthesis, while FUM19 (ATP-binding cassette transporter) acts as a repressor of the FUM cluster. The evolutionary conservation of FUM15 (P450 monooxygenase) in Fusarium and Aspergillus FUM clusters is discussed, and its effect on extracellular FB1 levels in both native (F. verticillioides) and heterologous (Saccharomyces cerevisiae) hosts is highlighted. These findings enhance our understanding of mycotoxin self-protection mechanisms and could inform strategies for predicting biological activity of unknown secondary metabolites, managing mycotoxin contamination, and developing resistant crop cultivars.https://journals.asm.org/doi/10.1128/mbio.02681-24Fusariumfumonisin B1FUM clusterself-protectionceramide biosynthesispalmitoyl-CoA ligase
spellingShingle Fabio Gherlone
Katarina Jojić
Ying Huang
Sandra Hoefgen
Vito Valiante
Slavica Janevska
The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
mBio
Fusarium
fumonisin B1
FUM cluster
self-protection
ceramide biosynthesis
palmitoyl-CoA ligase
title The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
title_full The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
title_fullStr The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
title_full_unstemmed The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
title_short The palmitoyl-CoA ligase Fum16 is part of a Fusarium verticillioides fumonisin subcluster involved in self-protection
title_sort palmitoyl coa ligase fum16 is part of a fusarium verticillioides fumonisin subcluster involved in self protection
topic Fusarium
fumonisin B1
FUM cluster
self-protection
ceramide biosynthesis
palmitoyl-CoA ligase
url https://journals.asm.org/doi/10.1128/mbio.02681-24
work_keys_str_mv AT fabiogherlone thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT katarinajojic thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT yinghuang thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT sandrahoefgen thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT vitovaliante thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT slavicajanevska thepalmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT fabiogherlone palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT katarinajojic palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT yinghuang palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT sandrahoefgen palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT vitovaliante palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection
AT slavicajanevska palmitoylcoaligasefum16ispartofafusariumverticillioidesfumonisinsubclusterinvolvedinselfprotection