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.
Cai, Feng M.
Ding, Mingyue
Jiang, Siqi
Atanasova, Lea
Baker, Scott E.
Barbosa-Filho, Jomal Rodrigues
Bayram Akcapinar, Gunseli
Brown, Daren W.
Chaverri, Priscila
Chen, Peijie
Chenthamara, Komal
Daum, Chris
Drula, Elodie
Dubey, Mukesh
Brandström Durling, Mikael
Flatschacher, Daniel
Ebner, Thomas
Emri, Tamás
Gao, Renwei
Georg, Raphaela Castro
Henrissat, Bernard
Hermosa, Rosa
Herrera-Estrella, Alfredo
Hinterdobler, Wolfgang
Kainz, Philipp
Karlsson, Magnus
Kredics, László
Kubicek, Christian P.
Kuo, Alan
LaButti, Kurt
Lipzen, Anna
Lorito, Matteo
Mach, Robert L.
Manganiello, Gelsomina
Marik, Tamás
Martinez-Reyes, Natalia
Mayrhofer-Reinhartshuber, Michael
Miskei, Márton
Moisan, Marie-Claude
Mondo, Stephen
Monte, Enrique
Ng, Vivian
Pang, Guan
Pangilinan, Jasmyn
Peng, Mao
Piombo, Edoardo
Pócsi, István
Rahimi, Mohammad Javad
Reddy, Sumitha K.
Riley, Robert
Sarrocco, Sabrina
Schmal, Matthias
Schmoll, Monika
Szűcs, Attila
Woo, Sheridan L.
Yarden, Oded
Zeilinger, Susanne
Zimmermann, Christian
Shelest, Ekaterina
Tsang, Adrian
Berka, Randy
de Vries, Ronald P.
Grigoriev, Igor V.
Druzhinina, Irina S.
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 name | Awards |
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
Rights statement
In Copyright
Additional information
IF = 19.4 (2024)