Lolium perenne apoplast metabolomics for identification of novel metabolites produced by the symbiotic fungus Epichloë festucae.


Journal

The New phytologist
ISSN: 1469-8137
Titre abrégé: New Phytol
Pays: England
ID NLM: 9882884

Informations de publication

Date de publication:
07 2020
Historique:
received: 08 12 2019
accepted: 28 02 2020
pubmed: 11 3 2020
medline: 15 5 2021
entrez: 11 3 2020
Statut: ppublish

Résumé

Epichloë festucae is an endophytic fungus that forms a symbiotic association with Lolium perenne. Here we analysed how the metabolome of the ryegrass apoplast changed upon infection of this host with sexual and asexual isolates of E. festucae. A metabolite fingerprinting approach was used to analyse the metabolite composition of apoplastic wash fluid from uninfected and infected L. perenne. Metabolites enriched or depleted in one or both of these treatments were identified using a set of interactive tools. A genetic approach in combination with tandem MS was used to identify a novel product of a secondary metabolite gene cluster. Metabolites likely to be present in the apoplast were identified using MarVis in combination with the BioCyc and KEGG databases, and an in-house Epichloë metabolite database. We were able to identify the known endophyte-specific metabolites, peramine and epichloëcyclins, as well as a large number of unknown markers. To determine whether these methods can be applied to the identification of novel Epichloë-derived metabolites, we deleted a gene encoding a NRPS (lgsA) that is highly expressed in planta. Comparative MS analysis of apoplastic wash fluid from wild-type- vs mutant-infected plants identified a novel Leu/Ile glycoside metabolite present in the former.

Identifiants

pubmed: 32155669
doi: 10.1111/nph.16528
pmc: PMC7317419
doi:

Substances chimiques

Fungal Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

559-571

Informations de copyright

© 2020 The Authors. New Phytologist © 2020 New Phytologist Trust.

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Auteurs

Kimberly A Green (KA)

School of Fundamental Sciences, Massey University, Palmerston North, 4442, New Zealand.
Bioprotection Research Centre, Massey University, Palmerston North, 4442, New Zealand.

Daniel Berry (D)

School of Fundamental Sciences, Massey University, Palmerston North, 4442, New Zealand.
Bioprotection Research Centre, Massey University, Palmerston North, 4442, New Zealand.

Kirstin Feussner (K)

Department of Plant Biochemistry, Albrecht von Haller Institute for Plant Sciences, University of Goettingen, D-37077, Goettingen, Germany.
Service Unit for Metabolomics and Lipidomics, Goettingen Center for Molecular Biosciences (GZMB), University of Goettingen, D-37077, Goettingen, Germany.

Carla J Eaton (CJ)

School of Fundamental Sciences, Massey University, Palmerston North, 4442, New Zealand.
Bioprotection Research Centre, Massey University, Palmerston North, 4442, New Zealand.

Arvina Ram (A)

School of Fundamental Sciences, Massey University, Palmerston North, 4442, New Zealand.

Carl H Mesarich (CH)

Bioprotection Research Centre, Massey University, Palmerston North, 4442, New Zealand.
School of Agriculture and Environment, Massey University, Palmerston North, 4442, New Zealand.

Peter Solomon (P)

Research School of Biology, Australian National University, Canberra, ACT, 0200, Australia.

Ivo Feussner (I)

Department of Plant Biochemistry, Albrecht von Haller Institute for Plant Sciences, University of Goettingen, D-37077, Goettingen, Germany.
Service Unit for Metabolomics and Lipidomics, Goettingen Center for Molecular Biosciences (GZMB), University of Goettingen, D-37077, Goettingen, Germany.
Department of Plant Biochemistry, Goettingen Center for Molecular Biosciences (GZMB), University of Goettingen, D-37077, Goettingen, Germany.

Barry Scott (B)

School of Fundamental Sciences, Massey University, Palmerston North, 4442, New Zealand.
Bioprotection Research Centre, Massey University, Palmerston North, 4442, New Zealand.

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Classifications MeSH