Evidence map›Paper›PMID 41382244›Full record

ArticleMicrobiome2025

Multi-meta-omics reveal unique symbiotic synchronization between ectomycorrhizal fungus and soil microbiome in Tricholoma matsutake habitat.

In Hyup Bae, Hyun Kim, Su-Min Kim, Yong-Hwan Lee

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Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

In Hyup Bae *Department of Agricultural Biotechnology, Seoul National University, Seoul, 08826, Republic of Korea.
Hyun Kim *Department of Agricultural Biotechnology, Seoul National University, Seoul, 08826, Republic of Korea. kh0219@snu.ac.kr.
Su-Min KimDepartment of Agricultural Biotechnology, Seoul National University, Seoul, 08826, Republic of Korea.
Yong-Hwan LeeDepartment of Agricultural Biotechnology, Seoul National University, Seoul, 08826, Republic of Korea. yonglee@snu.ac.kr.

Funding

National Research Foundation of Korea RS-2022-NR072199National Research Foundation of Korea RS-2025-00512558
6 · The paper itself

Abstract

backgroundEctomycorrhizal (ECM) fungi establish symbiotic relationships with plant roots, enhancing nutrient uptake, improving plant health, and boosting ecosystem resilience. Although previous studies reported molecular interactions among plant-ECM fungi-surrounding microbes near plant roots, microbiome-wide metabolic shifts and associations with the fungi remain unclear.

resultsUsing Tricholoma matsutake as a model, we initially found that T. matsutake induced remarkable microbial community turnover linked to altered soil moisture, nitrogen, and phosphorus levels. Parallel with the compositional alteration, microbiome-wide metabolic capacities, including glutamate metabolism, oligopeptide transport, and siderophore activity, were enriched in the T. matsutake-colonizing soil compared to the soils where the fungus was not colonized. From metatranscriptome data, we found that T. matsutake induced functional remodeling in nitrogen metabolism. Notably, the fungus and soil microbiome were metabolically synchronized with the upregulation of nitrate reduction, glutamate biosynthesis, tryptophan biosynthesis, and indole-3-acetic acid (IAA) biosynthesis. Metabarcoding and metatranscriptome-guided microbial associations revealed potential T. matsutake helper bacteria consisting of Conexibacter and Paraburkholderia. Phage community analyses further showed that the colonization of the ECM fungus influenced phage distributions along with the increase in temperate phage populations. The differential expression of auxiliary metabolic genes also demonstrated that phages could influence bacterial fitness in response to T. matsutake colonization.

conclusionOur multi-meta-omics-based approaches revealed unique environmental changes by T. matsutake compared to other mycorrhizal systems, as well as metabolic synchronization between the ECM fungus and surrounding microbiomes. These findings will expand our understanding of ECM symbiotic frameworks by highlighting integrated microbial and viral metabolic dynamics. Video Abstract.

Indexed as

MicrobiotaMycorrhizaeSoil MicrobiologySymbiosisTricholomaBacteriaEcosystemNitrogenPlant RootsSoilNitrogenSoilMetabolic synchronizationMetagenomicsMetatranscriptomicsMycorrhizal symbiosisTricholoma matsutake

Identifiers

PMID41382244
PMCPMC12801662

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.