Nature Communications (Sep 2023)

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

  • Kei Hiruma,
  • Seishiro Aoki,
  • Junya Takino,
  • Takeshi Higa,
  • Yuniar Devi Utami,
  • Akito Shiina,
  • Masanori Okamoto,
  • Masami Nakamura,
  • Nanami Kawamura,
  • Yoshihiro Ohmori,
  • Ryohei Sugita,
  • Keitaro Tanoi,
  • Toyozo Sato,
  • Hideaki Oikawa,
  • Atsushi Minami,
  • Wataru Iwasaki,
  • Yusuke Saijo

DOI
https://doi.org/10.1038/s41467-023-40867-w
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 18

Abstract

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Abstract 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.