Cargando…

Fungal endophyte infection of ryegrass reprograms host metabolism and alters development

Beneficial associations between plants and microbes play an important role in both natural and agricultural ecosystems. For example, associations between fungi of the genus Epichloë, and cool‐season grasses are known for their ability to increase resistance to insect pests, fungal pathogens and drou...

Descripción completa

Detalles Bibliográficos
Autores principales: Dupont, Pierre‐Yves, Eaton, Carla J., Wargent, Jason J., Fechtner, Susanne, Solomon, Peter, Schmid, Jan, Day, Robert C., Scott, Barry, Cox, Murray P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049663/
https://www.ncbi.nlm.nih.gov/pubmed/26305687
http://dx.doi.org/10.1111/nph.13614
_version_ 1782457763263152128
author Dupont, Pierre‐Yves
Eaton, Carla J.
Wargent, Jason J.
Fechtner, Susanne
Solomon, Peter
Schmid, Jan
Day, Robert C.
Scott, Barry
Cox, Murray P.
author_facet Dupont, Pierre‐Yves
Eaton, Carla J.
Wargent, Jason J.
Fechtner, Susanne
Solomon, Peter
Schmid, Jan
Day, Robert C.
Scott, Barry
Cox, Murray P.
author_sort Dupont, Pierre‐Yves
collection PubMed
description Beneficial associations between plants and microbes play an important role in both natural and agricultural ecosystems. For example, associations between fungi of the genus Epichloë, and cool‐season grasses are known for their ability to increase resistance to insect pests, fungal pathogens and drought. However, little is known about the molecular changes induced by endophyte infection. To study the impact of endophyte infection, we compared the expression profiles, based on RNA sequencing, of perennial ryegrass infected with Epichloë festucae with noninfected plants. We show that infection causes dramatic changes in the expression of over one third of host genes. This is in stark contrast to mycorrhizal associations, where substantially fewer changes in host gene expression are observed, and is more similar to pathogenic interactions. We reveal that endophyte infection triggers reprogramming of host metabolism, favouring secondary metabolism at a cost to primary metabolism. Infection also induces changes in host development, particularly trichome formation and cell wall biogenesis. Importantly, this work sheds light on the mechanisms underlying enhanced resistance to drought and super‐infection by fungal pathogens provided by fungal endophyte infection. Finally, our study reveals that not all beneficial plant–microbe associations behave the same in terms of their effects on the host.
format Online
Article
Text
id pubmed-5049663
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50496632016-10-06 Fungal endophyte infection of ryegrass reprograms host metabolism and alters development Dupont, Pierre‐Yves Eaton, Carla J. Wargent, Jason J. Fechtner, Susanne Solomon, Peter Schmid, Jan Day, Robert C. Scott, Barry Cox, Murray P. New Phytol Research Beneficial associations between plants and microbes play an important role in both natural and agricultural ecosystems. For example, associations between fungi of the genus Epichloë, and cool‐season grasses are known for their ability to increase resistance to insect pests, fungal pathogens and drought. However, little is known about the molecular changes induced by endophyte infection. To study the impact of endophyte infection, we compared the expression profiles, based on RNA sequencing, of perennial ryegrass infected with Epichloë festucae with noninfected plants. We show that infection causes dramatic changes in the expression of over one third of host genes. This is in stark contrast to mycorrhizal associations, where substantially fewer changes in host gene expression are observed, and is more similar to pathogenic interactions. We reveal that endophyte infection triggers reprogramming of host metabolism, favouring secondary metabolism at a cost to primary metabolism. Infection also induces changes in host development, particularly trichome formation and cell wall biogenesis. Importantly, this work sheds light on the mechanisms underlying enhanced resistance to drought and super‐infection by fungal pathogens provided by fungal endophyte infection. Finally, our study reveals that not all beneficial plant–microbe associations behave the same in terms of their effects on the host. John Wiley and Sons Inc. 2015-12 2015-08-25 /pmc/articles/PMC5049663/ /pubmed/26305687 http://dx.doi.org/10.1111/nph.13614 Text en © 2015 The Authors. New Phytologist © 2015 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dupont, Pierre‐Yves
Eaton, Carla J.
Wargent, Jason J.
Fechtner, Susanne
Solomon, Peter
Schmid, Jan
Day, Robert C.
Scott, Barry
Cox, Murray P.
Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title_full Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title_fullStr Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title_full_unstemmed Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title_short Fungal endophyte infection of ryegrass reprograms host metabolism and alters development
title_sort fungal endophyte infection of ryegrass reprograms host metabolism and alters development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049663/
https://www.ncbi.nlm.nih.gov/pubmed/26305687
http://dx.doi.org/10.1111/nph.13614
work_keys_str_mv AT dupontpierreyves fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT eatoncarlaj fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT wargentjasonj fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT fechtnersusanne fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT solomonpeter fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT schmidjan fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT dayrobertc fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT scottbarry fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment
AT coxmurrayp fungalendophyteinfectionofryegrassreprogramshostmetabolismandaltersdevelopment