Literature DB >> 31834634

An ectomycorrhizal fungus alters sensitivity to jasmonate, salicylate, gibberellin, and ethylene in host roots.

Veronica Basso1, Annegret Kohler1, Shingo Miyauchi1, Vasanth Singan2, Frédéric Guinet1, Jan Šimura3, Ondřej Novák3, Kerrie W Barry2, Mojgan Amirebrahimi2, Jonathan Block1, Yohann Daguerre1,4, Hyunsoo Na2, Igor V Grigoriev2,5, Francis Martin1,6, Claire Veneault-Fourrey.   

Abstract

The phytohormones jasmonate, gibberellin, salicylate, and ethylene regulate an interconnected reprogramming network integrating root development with plant responses against microbes. The establishment of mutualistic ectomycorrhizal symbiosis requires the suppression of plant defense responses against fungi as well as the modification of root architecture and cortical cell wall properties. Here, we investigated the contribution of phytohormones and their crosstalk to the ontogenesis of ectomycorrhizae (ECM) between grey poplar (Populus tremula x alba) roots and the fungus Laccaria bicolor. To obtain the hormonal blueprint of developing ECM, we quantified the concentrations of jasmonates, gibberellins, and salicylate via liquid chromatography-tandem mass spectrometry. Subsequently, we assessed root architecture, mycorrhizal morphology, and gene expression levels (RNA sequencing) in phytohormone-treated poplar lateral roots in the presence or absence of L. bicolor. Salicylic acid accumulated in mid-stage ECM. Exogenous phytohormone treatment affected the fungal colonization rate and/or frequency of Hartig net formation. Colonized lateral roots displayed diminished responsiveness to jasmonate but regulated some genes, implicated in defense and cell wall remodelling, that were specifically differentially expressed after jasmonate treatment. Responses to salicylate, gibberellin, and ethylene were enhanced in ECM. The dynamics of phytohormone accumulation and response suggest that jasmonate, gibberellin, salicylate, and ethylene signalling play multifaceted roles in poplar L. bicolor ectomycorrhizal development.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  zzm321990Laccaria bicolor; zzm321990Populus tremula x alba; MiSSP; cell wall remodelling; crosstalk; defense; ectomycorrhizae; jasmonate; phytohormones; symbiosis

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Substances:

Year:  2020        PMID: 31834634     DOI: 10.1111/pce.13702

Source DB:  PubMed          Journal:  Plant Cell Environ        ISSN: 0140-7791            Impact factor:   7.228


  5 in total

1.  Physiological and transcriptional responses of the ectomycorrhizal fungus Cenococcum geophilum to salt stress.

Authors:  Jiali Li; Chaofeng Li; Momi Tsuruta; Norihisa Matsushita; Susumu Goto; Zhenguo Shen; Daisuke Tsugama; Shijie Zhang; Chunlan Lian
Journal:  Mycorrhiza       Date:  2022-05-11       Impact factor: 3.387

Review 2.  Function and Mechanism of Jasmonic Acid in Plant Responses to Abiotic and Biotic Stresses.

Authors:  Yun Wang; Salma Mostafa; Wen Zeng; Biao Jin
Journal:  Int J Mol Sci       Date:  2021-08-09       Impact factor: 5.923

Review 3.  Role of Ectomycorrhizal Symbiosis Behind the Host Plants Ameliorated Tolerance Against Heavy Metal Stress.

Authors:  Eetika Chot; Mondem Sudhakara Reddy
Journal:  Front Microbiol       Date:  2022-03-28       Impact factor: 5.640

4.  Parametarhizium hingganense, a Novel Ectomycorrhizal Fungal Species, Promotes the Growth of Mung Beans and Enhances Resistance to Disease Induced by Rhizoctonia solani.

Authors:  Ying Gao; Siyu Gao; Yang Bai; Wei Meng; Lijian Xu
Journal:  J Fungi (Basel)       Date:  2022-09-02

Review 5.  Perception of lipo-chitooligosaccharides by the bioenergy crop Populus.

Authors:  Kevin R Cope; Thomas B Irving; Sanhita Chakraborty; Jean-Michel Ané
Journal:  Plant Signal Behav       Date:  2021-04-02
  5 in total

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