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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10482981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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