Evidence map›Paper›PMID 38441669›Full record

ArticleMycorrhiza2024

Sesquiterpenes of the ectomycorrhizal fungus Pisolithus microcarpus alter root growth and promote host colonization.

Jonathan M Plett, Dominika Wojtalewicz, Krista L Plett, Sabrina Collin, Annegret Kohler, Christophe Jacob, Francis Martin

Open access · hybridAbstract read
In one paragraph

Article in Mycorrhiza, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
10.2field-weighted citation impact, top 2% of its field
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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  8. IMA fungus · 2025
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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

7 authors at 4 institutions in 2 countries.

Jonathan M PlettHawkesbury Institute for the Environment, Western Sydney University, Richmond, NSW, 2753, Australia. j.plett@westernsydney.edu.au.ORCID http://orcid.org/0000-0003-0514-8146
Dominika WojtalewiczHawkesbury Institute for the Environment, Western Sydney University, Richmond, NSW, 2753, Australia.
Krista L PlettHawkesbury Institute for the Environment, Western Sydney University, Richmond, NSW, 2753, Australia.
Sabrina CollinUniversité de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
Annegret KohlerUniversité de Lorraine, INRAE, UMR Interactions Arbres-Microorganismes, Centre INRAE Grand Est-Nancy, 54280, Champenoux, France.
Christophe JacobUniversité de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
Francis MartinUniversité de Lorraine, INRAE, UMR Interactions Arbres-Microorganismes, Centre INRAE Grand Est-Nancy, 54280, Champenoux, France.
Centre National de la Recherche Scientifique · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRWestern Sydney University · AUNew South Wales Department of Primary Industries · AU

Funding

Agence Nationale de la Recherche ANR-11-LABX-0002-01Australian Research Council DE150100408
6 · The paper itself

Abstract

Trees form symbioses with ectomycorrhizal (ECM) fungi, maintained in part through mutual benefit to both organisms. Our understanding of the signaling events leading to the successful interaction between the two partners requires further study. This is especially true for understanding the role of volatile signals produced by ECM fungi. Terpenoids are a predominant class of volatiles produced by ECM fungi. While several ECM genomes are enriched in the enzymes responsible for the production of these volatiles (i.e., terpene synthases (TPSs)) when compared to other fungi, we have limited understanding of the biochemical products associated with each enzyme and the physiological impact of specific terpenes on plant growth. Using a combination of phylogenetic analyses, RNA sequencing, and functional characterization of five TPSs from two distantly related ECM fungi (Laccaria bicolor and Pisolithus microcarpus), we investigated the role of these secondary metabolites during the establishment of symbiosis. We found that despite phylogenetic divergence, these TPSs produced very similar terpene profiles. We focused on the role of P. microcarpus terpenes and found that the fungus expressed a diverse array of mono-, di-, and sesquiterpenes prior to contact with the host. However, these metabolites were repressed following physical contact with the host Eucalyptus grandis. Exposure of E. grandis to heterologously produced terpenes (enriched primarily in

Indexed as

BasidiomycotaMycorrhizaeSesquiterpenesPhylogenyPlant RootsSymbiosisSesquiterpenesFungusMycorrhizaPlant-microbe interactionRootSymbiosisTerpene synthase

Identifiers

PMID38441669
PMCPMC10998793
OpenAlexW4392470936

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.