Evidence map›Paper›PMID 42023699›Full record

ArticleTree physiology2026

Volatile cues from pathogenic, mutualistic and saprotrophic fungi cause specific, fungus-dependent responses in poplar.

Peiyuan Zhu, Baris Weber, Maaria Rosenkranz, Andrea Ghirardo, Jörg-Peter Schnitzler

Abstract read
In one paragraph

Article in Tree physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Peiyuan ZhuResearch Unit Environmental Simulation, Helmholtz Munich, Ingolstädter Landstraße 1, 85764 Neuherberg, Oberschleißheim, Bavaria, Germany.ORCID 0009-0004-6081-2278
Baris WeberResearch Unit Environmental Simulation, Helmholtz Munich, Ingolstädter Landstraße 1, 85764 Neuherberg, Oberschleißheim, Bavaria, Germany.ORCID 0000-0003-1179-4056
Maaria RosenkranzResearch Unit Environmental Simulation, Helmholtz Munich, Ingolstädter Landstraße 1, 85764 Neuherberg, Oberschleißheim, Bavaria, Germany.ORCID 0000-0002-1421-112X
Andrea GhirardoResearch Unit Environmental Simulation, Helmholtz Munich, Ingolstädter Landstraße 1, 85764 Neuherberg, Oberschleißheim, Bavaria, Germany.ORCID 0000-0003-1973-4007
Jörg-Peter SchnitzlerResearch Unit Environmental Simulation, Helmholtz Munich, Ingolstädter Landstraße 1, 85764 Neuherberg, Oberschleißheim, Bavaria, Germany.ORCID 0000-0002-9825-867X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants are exposed to complex interactions with belowground organisms, yet how they differentiate between mutualistic and pathogenic fungi before physical contact remains largely unknown. We exposed the roots of young Populus × canescens (Aiton) Sm. plants to volatile organic compounds (VOCs) emitted by fungi with contrasting lifestyles: the pathogenic Heterobasidion annosum (Fr.) Bref., the saprotrophPostia placenta (Fr.) M.J. Larsen & Lombard and the ectomycorrhizal fungus Laccaria bicolor (Maire) P.D. Orton. Volatile organic compound analysis of the shared rhizosphere headspace and leaf emissions revealed that poplar plants could perceive and respond to fungal identity solely through airborne cues. The root-zone headspace contained fungus-specific sesquiterpene fingerprints that remained similar after 3 and 6 weeks of co-cultivation: Pathogen-derived VOCs induced constantly high sesquiterpene emissions from the root-zone, whereas mycorrhizal VOCs caused low but targeted emissions of specific sesquiterpenes. In contrast, saprotrophic VOCs caused a temporal shift in root-zone VOC pattern, with increased sesquiterpene emissions after 6 weeks. Fungal VOC exposure also altered leaf VOC emissions, enriching alkanes, esters and monoterpenes. Initially, leaf VOC emissions were fungal lifestyle-specific but they converged over time, indicating systemic signal integration of belowground signals. These findings demonstrate that trees can discriminate 'friend-versus-foe' through VOCs alone, extending pattern-recognition theory beyond contact-dependent cues. Multivariate analyses suggested organ-specific chemical strategies: roots function as chemosensors decoding fungal volatilomes, while systemic adjustments shape aboveground VOC profiles. Understanding the plant response to fungal VOCs may offer potential for developing early pathogen diagnostics and further elucidate the volatile-mediated plant-fungal interactions.

Indexed as

BasidiomycotaLaccariaPopulusVolatile Organic CompoundsMycorrhizaePlant RootsSesquiterpenesSymbiosisSesquiterpenesVolatile Organic Compoundsbelowground-aboveground signalingchemical ecologylifestyle-specific recognitionplant defensePopulussesquiterpenesvolatile organic compounds (VOCs)

Identifiers

PMID42023699
PMCPMC13245404

What Socratic holds

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Registered trials

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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 Socratic graph.