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Nitrogen deprivation in Fusarium oxysporum promotes mycotoxin production via intermediates in the Krebs cycle and unreported methylmalonyl-CoA mutase activity.

Identifieur interne : 000D69 ( Main/Exploration ); précédent : 000D68; suivant : 000D70

Nitrogen deprivation in Fusarium oxysporum promotes mycotoxin production via intermediates in the Krebs cycle and unreported methylmalonyl-CoA mutase activity.

Auteurs : A V Karpe [Australie] ; M S Dunn [Australie] ; M C Taylor [Australie] ; T. Nguyen [Australie] ; C. Ong [Australie] ; T. Karla [Australie] ; S. Rockman [Australie] ; D J Beale [Australie]

Source :

RBID : pubmed:30830469

Descripteurs français

English descriptors

Abstract

INTRODUCTION

Fusarium oxysporum has a high affinity for lignin and cellulose-based substrates and is known to grow in a wide range of environments. It is these properties and its ability to produce mycotoxins that have contributed to its pathogenicity in cereal crops that can affect human and animal health when ingested.

OBJECTIVES

Identify the mechanisms of mycotoxin production and map the functional output of F. oxysporum under varying growth conditions.

METHODS

Liquid and gas-based chromatography coupled with mass spectrometry was used to identify and map the untargeted metabolic pathway of F. oxysporum grown using nitrogen limited and organic/inorganic nitrogen supplemented media.

RESULTS

Over 1300 metabolites were identified, relating to 42 metabolic pathways. Of these, 520 metabolites merged at pyruvate (glycolysis), succinate (Krebs cycle) and aspartate-glutamate metabolic pathways. CoA depletion at the growth stage triggered the initiation of fatty acid and branched amino acid degradation. This in turn activated propionyl CoA carnitine acetyltransferase enzymes, resulting in nitrogen preservation (urea, putrescine and organic acids end-products). CoA then transferred into the TCA cycle via previously unreported β-alanine and propionyl CoA metabolic pathways, the latter likely being a novel methylmalonyl-CoA mutase activity for F. oxysporum.

CONCLUSIONS

The lower supplementation of inorganic nitrogen compounds (≤ 50 mM) and the elimination of nitrates/organic nitrogen sources resulted in TCA autophagy events that boosted mycotoxin-based metabolism and decreased overall F. oxysporum growth. Such knowledge of functional mycotoxin production can be used to supplement agricultural crops and reduce the risk of mycotoxin contamination in human and animal food supplies.


DOI: 10.1007/s11306-018-1459-0
PubMed: 30830469


Affiliations:


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Le document en format XML

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<term>Citric Acid Cycle (MeSH)</term>
<term>Fusarium (growth & development)</term>
<term>Fusarium (metabolism)</term>
<term>Gas Chromatography-Mass Spectrometry (MeSH)</term>
<term>Metabolic Networks and Pathways (MeSH)</term>
<term>Metabolome (MeSH)</term>
<term>Methylmalonyl-CoA Mutase (metabolism)</term>
<term>Mycotoxins (analysis)</term>
<term>Mycotoxins (metabolism)</term>
<term>Nitrogen (deficiency)</term>
</keywords>
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<term>Azote (déficit)</term>
<term>Chromatographie gazeuse-spectrométrie de masse (MeSH)</term>
<term>Cycle citrique (MeSH)</term>
<term>Fusarium (croissance et développement)</term>
<term>Fusarium (métabolisme)</term>
<term>Methylmalonyl-coA mutase (métabolisme)</term>
<term>Mycotoxines (analyse)</term>
<term>Mycotoxines (métabolisme)</term>
<term>Métabolome (MeSH)</term>
<term>Voies et réseaux métaboliques (MeSH)</term>
</keywords>
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<term>Mycotoxins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="deficiency" xml:lang="en">
<term>Nitrogen</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Methylmalonyl-CoA Mutase</term>
<term>Mycotoxins</term>
</keywords>
<keywords scheme="MESH" qualifier="analyse" xml:lang="fr">
<term>Mycotoxines</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Fusarium</term>
</keywords>
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<term>Azote</term>
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<term>Fusarium</term>
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<term>Fusarium</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Fusarium</term>
<term>Methylmalonyl-coA mutase</term>
<term>Mycotoxines</term>
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<term>Gas Chromatography-Mass Spectrometry</term>
<term>Metabolic Networks and Pathways</term>
<term>Metabolome</term>
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<term>Chromatographie gazeuse-spectrométrie de masse</term>
<term>Cycle citrique</term>
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<term>Voies et réseaux métaboliques</term>
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<div type="abstract" xml:lang="en">
<p>
<b>INTRODUCTION</b>
</p>
<p>Fusarium oxysporum has a high affinity for lignin and cellulose-based substrates and is known to grow in a wide range of environments. It is these properties and its ability to produce mycotoxins that have contributed to its pathogenicity in cereal crops that can affect human and animal health when ingested.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVES</b>
</p>
<p>Identify the mechanisms of mycotoxin production and map the functional output of F. oxysporum under varying growth conditions.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Liquid and gas-based chromatography coupled with mass spectrometry was used to identify and map the untargeted metabolic pathway of F. oxysporum grown using nitrogen limited and organic/inorganic nitrogen supplemented media.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Over 1300 metabolites were identified, relating to 42 metabolic pathways. Of these, 520 metabolites merged at pyruvate (glycolysis), succinate (Krebs cycle) and aspartate-glutamate metabolic pathways. CoA depletion at the growth stage triggered the initiation of fatty acid and branched amino acid degradation. This in turn activated propionyl CoA carnitine acetyltransferase enzymes, resulting in nitrogen preservation (urea, putrescine and organic acids end-products). CoA then transferred into the TCA cycle via previously unreported β-alanine and propionyl CoA metabolic pathways, the latter likely being a novel methylmalonyl-CoA mutase activity for F. oxysporum.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The lower supplementation of inorganic nitrogen compounds (≤ 50 mM) and the elimination of nitrates/organic nitrogen sources resulted in TCA autophagy events that boosted mycotoxin-based metabolism and decreased overall F. oxysporum growth. Such knowledge of functional mycotoxin production can be used to supplement agricultural crops and reduce the risk of mycotoxin contamination in human and animal food supplies.</p>
</div>
</front>
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<AbstractText Label="RESULTS">Over 1300 metabolites were identified, relating to 42 metabolic pathways. Of these, 520 metabolites merged at pyruvate (glycolysis), succinate (Krebs cycle) and aspartate-glutamate metabolic pathways. CoA depletion at the growth stage triggered the initiation of fatty acid and branched amino acid degradation. This in turn activated propionyl CoA carnitine acetyltransferase enzymes, resulting in nitrogen preservation (urea, putrescine and organic acids end-products). CoA then transferred into the TCA cycle via previously unreported β-alanine and propionyl CoA metabolic pathways, the latter likely being a novel methylmalonyl-CoA mutase activity for F. oxysporum.</AbstractText>
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<Affiliation>Land & Water, CSIRO, Ecosciences Precinct, Dutton Park, QLD, 4102, Australia. david.beale@csiro.au.</Affiliation>
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