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A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae

Plant-associated fungi show diverse lifestyles from pathogenic to mutualistic to the host; however, the principles and mechanisms through which they shift the lifestyles require elucidation. The root fungus Colletotrichum tofieldiae (Ct) promotes Arabidopsis thaliana growth under phosphate limiting...

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Autores principales: Hiruma, Kei, Aoki, Seishiro, Takino, Junya, Higa, Takeshi, Utami, Yuniar Devi, Shiina, Akito, Okamoto, Masanori, Nakamura, Masami, Kawamura, Nanami, Ohmori, Yoshihiro, Sugita, Ryohei, Tanoi, Keitaro, Sato, Toyozo, Oikawa, Hideaki, Minami, Atsushi, Iwasaki, Wataru, Saijo, Yusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482981/
https://www.ncbi.nlm.nih.gov/pubmed/37673872
http://dx.doi.org/10.1038/s41467-023-40867-w
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author Hiruma, Kei
Aoki, Seishiro
Takino, Junya
Higa, Takeshi
Utami, Yuniar Devi
Shiina, Akito
Okamoto, Masanori
Nakamura, Masami
Kawamura, Nanami
Ohmori, Yoshihiro
Sugita, Ryohei
Tanoi, Keitaro
Sato, Toyozo
Oikawa, Hideaki
Minami, Atsushi
Iwasaki, Wataru
Saijo, Yusuke
author_facet Hiruma, Kei
Aoki, Seishiro
Takino, Junya
Higa, Takeshi
Utami, Yuniar Devi
Shiina, Akito
Okamoto, Masanori
Nakamura, Masami
Kawamura, Nanami
Ohmori, Yoshihiro
Sugita, Ryohei
Tanoi, Keitaro
Sato, Toyozo
Oikawa, Hideaki
Minami, Atsushi
Iwasaki, Wataru
Saijo, Yusuke
author_sort Hiruma, Kei
collection PubMed
description Plant-associated fungi show diverse lifestyles from pathogenic to mutualistic to the host; however, the principles and mechanisms through which they shift the lifestyles require elucidation. The root fungus Colletotrichum tofieldiae (Ct) promotes Arabidopsis thaliana growth under phosphate limiting conditions. Here we describe a Ct strain, designated Ct3, that severely inhibits plant growth. Ct3 pathogenesis occurs through activation of host abscisic acid pathways via a fungal secondary metabolism gene cluster related to the biosynthesis of sesquiterpene metabolites, including botrydial. Cluster activation during root infection suppresses host nutrient uptake-related genes and changes mineral contents, suggesting a role in manipulating host nutrition state. Conversely, disruption or environmental suppression of the cluster renders Ct3 beneficial for plant growth, in a manner dependent on host phosphate starvation response regulators. Our findings indicate that a fungal metabolism cluster provides a means by which infectious fungi modulate lifestyles along the parasitic–mutualistic continuum in fluctuating environments.
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spelling pubmed-104829812023-09-08 A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae Hiruma, Kei Aoki, Seishiro Takino, Junya Higa, Takeshi Utami, Yuniar Devi Shiina, Akito Okamoto, Masanori Nakamura, Masami Kawamura, Nanami Ohmori, Yoshihiro Sugita, Ryohei Tanoi, Keitaro Sato, Toyozo Oikawa, Hideaki Minami, Atsushi Iwasaki, Wataru Saijo, Yusuke Nat Commun Article Plant-associated fungi show diverse lifestyles from pathogenic to mutualistic to the host; however, the principles and mechanisms through which they shift the lifestyles require elucidation. The root fungus Colletotrichum tofieldiae (Ct) promotes Arabidopsis thaliana growth under phosphate limiting conditions. Here we describe a Ct strain, designated Ct3, that severely inhibits plant growth. Ct3 pathogenesis occurs through activation of host abscisic acid pathways via a fungal secondary metabolism gene cluster related to the biosynthesis of sesquiterpene metabolites, including botrydial. Cluster activation during root infection suppresses host nutrient uptake-related genes and changes mineral contents, suggesting a role in manipulating host nutrition state. Conversely, disruption or environmental suppression of the cluster renders Ct3 beneficial for plant growth, in a manner dependent on host phosphate starvation response regulators. Our findings indicate that a fungal metabolism cluster provides a means by which infectious fungi modulate lifestyles along the parasitic–mutualistic continuum in fluctuating environments. Nature Publishing Group UK 2023-09-06 /pmc/articles/PMC10482981/ /pubmed/37673872 http://dx.doi.org/10.1038/s41467-023-40867-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hiruma, Kei
Aoki, Seishiro
Takino, Junya
Higa, Takeshi
Utami, Yuniar Devi
Shiina, Akito
Okamoto, Masanori
Nakamura, Masami
Kawamura, Nanami
Ohmori, Yoshihiro
Sugita, Ryohei
Tanoi, Keitaro
Sato, Toyozo
Oikawa, Hideaki
Minami, Atsushi
Iwasaki, Wataru
Saijo, Yusuke
A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title_full A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title_fullStr A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title_full_unstemmed A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title_short A fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in Colletotrichum tofieldiae
title_sort fungal sesquiterpene biosynthesis gene cluster critical for mutualist-pathogen transition in colletotrichum tofieldiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482981/
https://www.ncbi.nlm.nih.gov/pubmed/37673872
http://dx.doi.org/10.1038/s41467-023-40867-w
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