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The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains

Grapevine trunk diseases (GTDs) affect grape production and reduce vineyard longevity worldwide. Since the causative fungi also occur in asymptomatic trunks, we address disease outbreak in terms of altered chemical communication between host and endophyte. Here, we identified four chemically similar...

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Autores principales: Guan, Pingyin, Schmidt, Florian, Fischer, Jochen, Riemann, Michael, Thines, Eckhard, Nick, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343913/
https://www.ncbi.nlm.nih.gov/pubmed/35928402
http://dx.doi.org/10.1093/hr/uhac120
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author Guan, Pingyin
Schmidt, Florian
Fischer, Jochen
Riemann, Michael
Thines, Eckhard
Nick, Peter
author_facet Guan, Pingyin
Schmidt, Florian
Fischer, Jochen
Riemann, Michael
Thines, Eckhard
Nick, Peter
author_sort Guan, Pingyin
collection PubMed
description Grapevine trunk diseases (GTDs) affect grape production and reduce vineyard longevity worldwide. Since the causative fungi also occur in asymptomatic trunks, we address disease outbreak in terms of altered chemical communication between host and endophyte. Here, we identified four chemically similar secondary metabolites secreted by the GTD-associated fungus Eutypa lata to analyse their modes of action in a grapevine cell culture of Vitis rupestris, where microtubules were tagged by GFP. Treatment with the metabolite eutypine activated defence responses, evident from extracellular alkalinisation and induction of defence genes. Eutypinol, instead, eliminated microtubules, in contrast to the other three compounds. Furthermore, we evaluated the effect of four corresponding chemical analogues of these compounds, sharing the phenolic but lacking the alkyne moiety. These analogues were able to induce similar defence responses in V. rupestris cells, albeit at reduced amplitude. Since closely related moieties differing only in details of the side groups at the phenolic ring differ significantly with respect to the response of the host cell, we propose that these fungal compounds act through a specific binding site at the membrane of grapevine cells. We corroborate this specificity by combination experiments, where the eutypine and the eutypinol analogues behave competitively with respect to the elicited responses. In summary, Eutypa lata secretes compounds that elicit host defence in a specific manner by interfering with early events of immunity signalling. This supports the notion that a real understanding of GTDs has to address inter-organismic chemical communication.
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spelling pubmed-93439132022-08-03 The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains Guan, Pingyin Schmidt, Florian Fischer, Jochen Riemann, Michael Thines, Eckhard Nick, Peter Hortic Res Article Grapevine trunk diseases (GTDs) affect grape production and reduce vineyard longevity worldwide. Since the causative fungi also occur in asymptomatic trunks, we address disease outbreak in terms of altered chemical communication between host and endophyte. Here, we identified four chemically similar secondary metabolites secreted by the GTD-associated fungus Eutypa lata to analyse their modes of action in a grapevine cell culture of Vitis rupestris, where microtubules were tagged by GFP. Treatment with the metabolite eutypine activated defence responses, evident from extracellular alkalinisation and induction of defence genes. Eutypinol, instead, eliminated microtubules, in contrast to the other three compounds. Furthermore, we evaluated the effect of four corresponding chemical analogues of these compounds, sharing the phenolic but lacking the alkyne moiety. These analogues were able to induce similar defence responses in V. rupestris cells, albeit at reduced amplitude. Since closely related moieties differing only in details of the side groups at the phenolic ring differ significantly with respect to the response of the host cell, we propose that these fungal compounds act through a specific binding site at the membrane of grapevine cells. We corroborate this specificity by combination experiments, where the eutypine and the eutypinol analogues behave competitively with respect to the elicited responses. In summary, Eutypa lata secretes compounds that elicit host defence in a specific manner by interfering with early events of immunity signalling. This supports the notion that a real understanding of GTDs has to address inter-organismic chemical communication. Oxford University Press 2022-06-01 /pmc/articles/PMC9343913/ /pubmed/35928402 http://dx.doi.org/10.1093/hr/uhac120 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nanjing Agricultural University https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Guan, Pingyin
Schmidt, Florian
Fischer, Jochen
Riemann, Michael
Thines, Eckhard
Nick, Peter
The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title_full The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title_fullStr The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title_full_unstemmed The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title_short The fungal elicitor eutypine from Eutypa lata activates basal immunity through its phenolic side chains
title_sort fungal elicitor eutypine from eutypa lata activates basal immunity through its phenolic side chains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343913/
https://www.ncbi.nlm.nih.gov/pubmed/35928402
http://dx.doi.org/10.1093/hr/uhac120
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