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  5. Phenogenomics reveals the ecology and evolution of Trichoderma fungi for sustainable agriculture.

Phenogenomics reveals the ecology and evolution of Trichoderma fungi for sustainable agriculture.

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Resource type
Journal article
Creator (person)
Steindorff, Andrei S.
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Cai, Feng M.
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Ding, Mingyue
Jiang, Siqi
Atanasova, Lea
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Baker, Scott E.
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Barbosa-Filho, Jomal Rodrigues
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Bayram Akcapinar, Gunseli
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Brown, Daren W.
Chaverri, Priscila
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Chen, Peijie
Chenthamara, Komal
Daum, Chris
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Drula, Elodie
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Dubey, Mukesh
Brandström Durling, Mikael
Flatschacher, Daniel
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Ebner, Thomas
Emri, Tamás
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Gao, Renwei
Georg, Raphaela Castro
Henrissat, Bernard
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Hermosa, Rosa
Herrera-Estrella, Alfredo
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Hinterdobler, Wolfgang
Kainz, Philipp
Karlsson, Magnus
Kredics, László
Kubicek, Christian P.
Kuo, Alan
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LaButti, Kurt
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Lipzen, Anna
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Lorito, Matteo
Mach, Robert L.
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Manganiello, Gelsomina
Marik, Tamás
Martinez-Reyes, Natalia
Mayrhofer-Reinhartshuber, Michael
Miskei, Márton
Moisan, Marie-Claude
Mondo, Stephen
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Monte, Enrique
Ng, Vivian
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Pang, Guan
Pangilinan, Jasmyn
Peng, Mao
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Piombo, Edoardo
Pócsi, István
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Rahimi, Mohammad Javad
Reddy, Sumitha K.
Riley, Robert
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Sarrocco, Sabrina
Schmal, Matthias
Schmoll, Monika
Szűcs, Attila
Woo, Sheridan L.
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Yarden, Oded
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Zeilinger, Susanne
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Zimmermann, Christian
Shelest, Ekaterina
Tsang, Adrian
Berka, Randy
de Vries, Ronald P.
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Grigoriev, Igor V.
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Druzhinina, Irina S.
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Date published
March 3, 2026
Abstract
Trichoderma fungi support sustainable agriculture by suppressing plant diseases and improving crop performance. However, emerging pathogenicity of Trichoderma warrants further ecological and genetic characterization. Here we used machine learning to correlate genomic data from 37 Trichoderma strains with over 140 phenotypic traits, spanning metabolic versatility, biotic interactions, stress tolerance and reproductive strategies. We determined Trichoderma to be an ancient, genetically cohesive and physiologically diverse genus with spores capable of germination in water and dispersal via air and water droplets. Metabolic preferences indicate universal adaptation to mycoparasitism and to niches like arboreal microbial mats, alongside broader saprotrophic versatility. Our analyses are consistent with character displacement among close relatives and convergent evolution in distant lineages, with both processes shaping ecological plasticity and traits including dispersal modes, terrestrialization or endophytism. Our findings reveal that while some Trichoderma species show traits of biosafety concern, its vast ecophysiological diversity enables the development of safe, targeted bioeffectors.
Project(s)
Priority 4: Accelerated Taxonomy
Funder
Funder nameAwards
Royal Botanic Gardens, Kew
Nanjing Agricultural University, China
National Natural Science Foundation of China, China
32470020
National Science Foundation, United States
DEB-1638976 - DEB-1019972
Ministry of Education of the People's Republic of China, China
Fundamental and Interdisciplinary Disciplines Breakthrough Plan (JYB2025XDXM902)
Hungarian Research Network, Hungary
Agricultural Research Service, United States
Conselho Nacional de Desenvolvimento Científico e Tecnológico, Brazil
Fundação de Amparo à Pesquisa do Estado de Goiás, Brazil
Sveriges Lantbruksuniversitet, Sweden
Journal title
Nature Microbiology
Volume
11
Publisher
Springer Science and Business Media LLC
Place of publication
Berlin/Heidelberg, Germany
eISSN
2058-5276
Date accepted
January 8, 2026
Official URL
https://doi.org/10.1038/s41564-026-02260-3
Related URL
https://www.nature.com/articles/s41564-026-02260-3
Rights statement
In Copyright
Licence
https://creativecommons.org/licenses/by/4.0/
DOI
10.1038/s41564-026-02260-3
Keywords
Sustainable agriculture
Crop performance
Trichoderma
Plant diseases
Phenogenomics
Additional information
IF = 19.4 (2024)
Managed by the British Library and supported by the AHRC

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