Evidence map›Paper›PMID 39856539›Full record

ArticleBMC plant biology2025

Transcriptional time-course analysis during ash dieback infection revealed different responses in tolerant and susceptible Fraxinus excelsior genotypes.

Víctor Chano, Renata Callegari Ferrari, Tania Domínguez-Flores, Karuna Shrestha, Barbara Fussi, Hannes Seidel, Oliver Gailing, Katharina B Budde

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

8 authors.

Víctor Chano *Department of Forest Genetics and Forest Tree Breeding, University of Göttingen, Büsgenweg 2, Göttingen, 37077, Germany. victor.chano@uni-goettingen.de.ORCID http://orcid.org/0000-0002-3423-9090
Renata Callegari Ferrari *Department of Forest Genetics and Forest Tree Breeding, University of Göttingen, Büsgenweg 2, Göttingen, 37077, Germany.ORCID http://orcid.org/0000-0002-9497-8442
Tania Domínguez-FloresDepartment of Forest Genetics and Forest Tree Breeding, University of Göttingen, Büsgenweg 2, Göttingen, 37077, Germany.ORCID http://orcid.org/0000-0002-4065-8224
Karuna ShresthaDepartment of Forest Genetics and Forest Tree Breeding, University of Göttingen, Büsgenweg 2, Göttingen, 37077, Germany.ORCID http://orcid.org/0009-0006-2625-860X
Barbara FussiBavarian Office for Forest Genetics (AWG), Forstamtsplatz 1, Teisendorf, 83317, Germany.ORCID http://orcid.org/0000-0002-7104-3935
Hannes SeidelBavarian Office for Forest Genetics (AWG), Forstamtsplatz 1, Teisendorf, 83317, Germany.ORCID https://orcid.org/0009-0008-0859-5850
Oliver GailingDepartment of Forest Genetics and Forest Tree Breeding, University of Göttingen, Büsgenweg 2, Göttingen, 37077, Germany. ogailin@gwdg.de.ORCID http://orcid.org/0000-0002-4572-2408
Katharina B BuddeNorthwest German Forest Research Institute, Professor-Oelkers-Straße 6, Hann. Münden, 34346, Germany.ORCID http://orcid.org/0000-0002-5361-2815

Funding

Bundesministerium für Ernährung und Landwirtschaft 2219WK21F4
6 · The paper itself

Abstract

Hymenoscyphus fraxineus, the causal agent of Ash Dieback (ADB), has been introduced to eastern Europe in the 1990s from where it spread causing decline in European ash populations. However, the genetic basis of the molecular response in tolerant and susceptible ash trees to this disease is still largely unknown. We performed RNA-sequencing to study the transcriptomic response to the disease in four ash genotypes (ADB-tolerant FAR3 and FS36, and ADB-susceptible UW1 and UW2), during a time-course of 7, 14, 21, and 28 days post-inoculation, including mock-inoculated trees as control samples for each sampling time point. The analysis yielded 395 and 500 Differentially Expressed Genes (DEGs) along the response for ADB-tolerant FAR3 and FS36, respectively, while ADB-susceptible UW1 and UW2 revealed 194 and 571 DEGs, respectively, with most DEGs found exclusively in just one of the genotypes. DEGs shared between tolerant genotypes FAR3 and FS36, included genes involved in the production of phytoalexins and other secondary metabolites with roles in plant defense. Moreover, we identified an earlier expression of genes involved in both pattern- and effector-triggered immunity (PTI and ETI) in ADB-tolerant genotypes, while in ADB-susceptible genotypes both responses were delayed (late response). Overall, these results revealed different transcriptomic expression patterns not only between ADB-tolerant and ADB-susceptible genotypes, but also within these two groups. This hints to individual responses in the natural tolerance to ADB, possibly revealing diversified strategies across ash genotypes.

Indexed as

AscomycotaFraxinusPlant DiseasesGene Expression ProfilingGene Expression Regulation, PlantGenotypeTranscriptomeEuropean ashGene expression analysisHymenoscyphus fraxineusRNA-SeqTime-series

Identifiers

PMID39856539
PMCPMC11762065

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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.