Evidence map›Paper›PMID 37968441›Full record

ArticleScientific reports2023

Mycoparasitism related targets of Tmk1 indicate stimulating regulatory functions of this MAP kinase in Trichoderma atroviride.

Lea Atanasova, Martina Marchetti-Deschmann, Albert Nemes, Bianca Bruckner, Pavel Rehulka, Nancy Stralis-Pavese, Paweł P Łabaj, David P Kreil, Susanne Zeilinger

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. HarnessingPlants (Basel, Switzerland) · 2026
    Review
  2. Mechanisms of action and biocontrol potential ofFrontiers in fungal biology · 2026
    Review
  3. Review
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

9 authors at 4 institutions in 3 countries.

Lea Atanasova *Department of Food Science and Technology, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria. lea.atanasova@boku.ac.at.
Martina Marchetti-Deschmann *Institute of Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.
Albert NemesInstitute of Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.
Bianca BrucknerInstitute of Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.
Pavel RehulkaInstitute of Chemical Technologies and Analytics, TU Wien (Vienna University of Technology), Vienna, Austria.
Nancy Stralis-PaveseIMBT Bioinformatics, Department of Biotechnology, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria.
Paweł P ŁabajIMBT Bioinformatics, Department of Biotechnology, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria.
David P KreilIMBT Bioinformatics, Department of Biotechnology, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria. david.kreil@boku.ac.at.
Susanne ZeilingerDepartment of Microbiology, Universität Innsbruck, Innsbruck, Austria. susanne.zeilinger@uibk.ac.at.
BOKU University · ATTU Wien · ATUniversität Innsbruck · ATUniversity of Defence · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycoparasitism is a key feature of Trichoderma (Hypocreales, Ascomycota) biocontrol agents. Recent studies of intracellular signal transduction pathways of the potent mycoparasite Trichoderma atroviride revealed the involvement of Tmk1, a mitogen-activated protein kinase (MAPK), in triggering the mycoparasitic response. We previously showed that mutants missing Tmk1 exhibit reduced mycoparasitic activity against several plant pathogenic fungi. In this study, we identified the most robustly regulated targets that were governed by Tmk1 during mycoparasitism using transcriptome and proteome profiling. Tmk1 mainly exerts a stimulating function for T. atroviride during its mycoparasitic interaction with the fungal plant pathogen Rhizoctonia solani, as reflected by 89% of strongly differently responding genes in the ∆tmk1 mutant compared to the wild type. Specifically, 54% of these genes showed strong downregulation in the response with a deletion of the tmk1 gene, whereas in the wild type the same genes were strongly upregulated during the interaction with the fungal host. These included the gene encoding the mycoparasitism-related proteinase Prb1; genes involved in signal transduction pathways such as a candidate coding for a conserved 14-3-3 protein, and a gene coding for Tmk2, the T. atroviride cell-wall integrity MAP kinase; genes encoding a specific siderophore synthetase, and multiple FAD-dependent oxidoreductases and aminotransferases. Due to the phosphorylating activity of Tmk1, different (phospho-)proteomics approaches were applied and identified proteins associated with cellular metabolism, energy production, protein synthesis and fate, and cell organization. Members of FAD- and NAD/NADP-binding-domain proteins, vesicular trafficking of molecules between cellular organelles, fungal translational, as well as protein folding apparatus were among others found to be phosphorylated by Tmk1 during mycoparasitism. Outstanding downregulation in the response of the ∆tmk1 mutant to the fungal host compared to the wild type at both the transcriptome and the proteome levels was observed for nitrilase, indicating that its defense and detoxification functions might be greatly dependent on Tmk1 during T. atroviride mycoparasitism. An intersection network analysis between the identified transcripts and proteins revealed a strong involvement of Tmk1 in molecular functions with GTPase and oxidoreductase activity. These data suggest that during T. atroviride mycoparasitism this MAPK mainly governs processes regulating cell responses to extracellular signals and those involved in reactive oxygen stress.

Indexed as

HypocrealesTrichodermaGene Expression Regulation, FungalMitogen-Activated Protein KinasesProteomeSignal TransductionMitogen-Activated Protein KinasesProteome

Identifiers

PMID37968441
PMCPMC10651915
OpenAlexW4388698079

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.