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Glauser, Gaëtan

Nom
Glauser, Gaëtan
Affiliation principale
Email
gaetan.glauser@unine.ch
Identifiants
https://libra.unine.ch/handle/123456789/369
_
0000-0002-0983-8614

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  • Publication
    Métadonnées seulement
    Metabolomics reveals herbivore-induced metabolites of resistance and susceptibility in maize leaves and roots
    (2013)
    Marti, Guillaume
    ;
    Erb, Matthias 
    ;
    Boccard, J.
    ;
    Glauser, Gaëtan 
    ;
    Doyen, G. R.
    ;
    Villard, Neil 
    ;
    Robert, Christelle Aurélie Maud
    ;
    Turlings, Ted 
    ;
    Rudaz, S.
    ;
    Wolfender, Jean-Luc
    Plants respond to herbivory by reprogramming their metabolism. Most research in this context has focused on locally induced compounds that function as toxins or feeding deterrents. We developed an ultra-high-pressure liquid chromatography time-of-flight mass spectrometry (UHPLC-TOF-MS)-based metabolomics approach to evaluate local and systemic herbivore-induced changes in maize leaves, sap, roots and root exudates without any prior assumptions about their function. Thirty-two differentially regulated compounds were identified from Spodoptera littoralis-infested maize seedlings and isolated for structure assignment by microflow nuclear magnetic resonance (CapNMR). Nine compounds were quantified by a high throughput direct nano-infusion tandem mass spectrometry/mass spectrometry (MS/MS) method. Leaf infestation led to a marked local increase of 1,3-benzoxazin-4-ones, phospholipids, N-hydroxycinnamoyltyramines, azealic acid and tryptophan. Only few changes were found in the root metabolome, but 1,3-benzoxazin-4-ones increased in the vascular sap and root exudates. The role of N-hydroxycinnamoyltyramines in plantherbivore interactions is unknown, and we therefore tested the effect of the dominating p-coumaroyltyramine on S. littoralis. Unexpectedly, p-coumaroyltyramine was metabolized by the larvae and increased larval growth, possibly by providing additional nitrogen to the insect. Taken together, this study illustrates that herbivore attack leads to the induction of metabolites that can have contrasting effects on herbivore resistance in the leaves and roots.
  • Publication
    Métadonnées seulement
    A specialist root herbivore exploits defensive metabolites to locate nutritious tissues
    (2012)
    Robert, Christelle Aurélie Maud
    ;
    Veyrat, Nathalie 
    ;
    Glauser, Gaëtan 
    ;
    Marti, Guillaume
    ;
    Doyen, G. R.
    ;
    Villard, Neil 
    ;
    Gaillard, Mickaël David Philippe
    ;
    Köllner, Tobias G.
    ;
    Giron, David
    ;
    Body, Mélanie
    ;
    Babst, Benjamin A.
    ;
    Ferrieri, Richard A.
    ;
    Turlings, Ted 
    ;
    Erb, Matthias 
    The most valuable organs of plants are often particularly rich in essential elements, but also very well defended. This creates a dilemma for herbivores that need to maximise energy intake while minimising intoxication. We investigated how the specialist root herbivore Diabrotica virgifera solves this conundrum when feeding on wild and cultivated maize plants. We found that crown roots of maize seedlings were vital for plant development and, in accordance, were rich in nutritious primary metabolites and contained higher amounts of the insecticidal 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) and the phenolic compound chlorogenic acid. The generalist herbivores Diabrotica balteata and Spodoptera littoralis were deterred from feeding on crown roots, whereas the specialist D. virgifera preferred and grew best on these tissues. Using a 1,4-benzoxazin-3-one-deficient maize mutant, we found that D. virgifera is resistant to DIMBOA and other 1,4-benzoxazin-3-ones and that it even hijacks these compounds to optimally forage for nutritious roots.
  • Publication
    Métadonnées seulement
    Induction and detoxification of maize 1,4-benzoxazin-3-ones by insect herbivores
    (2011)
    Glauser, Gaëtan 
    ;
    Marti, Guillaume
    ;
    Villard, Neil 
    ;
    Doyen, Gwladys A.
    ;
    Wolfender, Jean-Luc
    ;
    Turlings, Ted 
    ;
    Erb, Matthias 
    In monocotyledonous plants, 1,4-benzoxazin-3-ones, also referred to as benzoxazinoids or hydroxamic acids, are one of the most important chemical barriers against herbivores. However, knowledge about their behavior after attack, mode of action and potential detoxification by specialized insects remains limited. We chose an innovative analytical approach to understand the role of maize 1,4-benzoxazin-3-ones in plant?insect interactions. By combining unbiased metabolomics screening and simultaneous measurements of living and digested plant tissue, we created a quantitative dynamic map of 1,4-benzoxazin-3-ones at the plant?insect interface. Hypotheses derived from this map were tested by specifically developed in vitro assays using purified 1,4-benzoxazin-3-ones and active extracts from mutant plants lacking 1,4-benzoxazin-3-ones. Our data show that maize plants possess a two-step defensive system that effectively fends off both the generalist Spodoptera littoralis and the specialist Spodoptera frugiperda. In the first step, upon insect attack, large quantities of 2-?-d-glucopyranosyloxy-4,7-dimethoxy-1,4-benzoxazin-3-one (HDMBOA-Glc) are formed. In the second step, after tissue disruption by the herbivores, highly unstable 2-hydroxy-4,7-dimethoxy-1,4-benzoxazin-3-one (HDMBOA) is released by plant-derived ?-glucosidases. HDMBOA acts as a strong deterrent to both S. littoralis and S. frugiperda. Although constitutively produced 1,4-benzoxazin-3-ones such as 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) are detoxified via glycosylation by the insects, no conjugation of HDMBOA in the insect gut was found, which may explain why even the specialist S. frugiperda has not evolved immunity against this plant defense. Taken together, our results show the benefit of using a plant?insect interface approach to elucidate plant defensive processes and unravel a potent resistance mechanism in maize.
  • Publication
    Métadonnées seulement
    Chloroplast lipid droplet type II NAD(P)H quinone oxidoreductase is essential for prenylquinone metabolism and vitamin K1 accumulation
    (2011)
    Eugeni Piller, Lucia
    ;
    Besagni, Celine 
    ;
    Ksas, Brigitte
    ;
    Rumeau, Dominique
    ;
    Bréhélin, Claire
    ;
    Glauser, Gaëtan 
    ;
    Kessler, Félix 
    ;
    Havaux, Michel
    Lipid droplets are ubiquitous cellular structures in eukaryotes and are required for lipid metabolism. Little is currently known about plant lipid droplets other than oil bodies. Here, we define dual roles for chloroplast lipid droplets (plastoglobules) in energy and prenylquinone metabolism. The prenylquinones?plastoquinone, plastochromanol-8, phylloquinone (vitamin K1), and tocopherol (vitamin E)?are partly stored in plastoglobules. This work shows that NAD(P)H dehydrogenase C1 (NDC1) (At5g08740), a type II NAD(P)H quinone oxidoreductase, associates with plastoglobules. NDC1 reduces a plastoquinone analog in vitro and affects the overall redox state of the total plastoquinone pool in vivo by reducing the plastoquinone reservoir of plastoglobules. Finally, NDC1 is required for normal plastochromanol-8 accumulation and is essential for vitamin K1 production.