Evidence map›Paper›PMID 38806462›Full record

ArticleNature communications2024

Physiochemical interaction between osmotic stress and a bacterial exometabolite promotes plant disease.

Felix Getzke, Lei Wang, Guillaume Chesneau, Nils Böhringer, Fantin Mesny, Nienke Denissen, Hidde Wesseler, Priscilla Tijesuni Adisa, Michael Marner, Paul Schulze-Lefert and 2 more

Abstract read
In one paragraph

Article in Nature communications, 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
–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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Dynamic shifts in plant-microbe relationships.Plant biotechnology (Tokyo, Japan) · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
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

12 authors.

Felix Getzke *Department of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.
Lei Wang *Institute for Insect Biotechnology, Justus-Liebig-University Giessen, 35392, Giessen, Germany.
Guillaume ChesneauDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.
Nils BöhringerInstitute for Insect Biotechnology, Justus-Liebig-University Giessen, 35392, Giessen, Germany.
Fantin MesnyDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.ORCID http://orcid.org/0000-0002-3044-1398
Nienke DenissenDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.
Hidde WesselerDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.
Priscilla Tijesuni AdisaDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.
Michael MarnerFraunhofer Institute for Molecular Biology and Applied Ecology (IME), Branch for Bioresources, 35392, Giessen, Germany.ORCID http://orcid.org/0000-0002-1024-1567
Paul Schulze-LefertDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany.ORCID http://orcid.org/0000-0002-8978-1717
Till F SchäberleInstitute for Insect Biotechnology, Justus-Liebig-University Giessen, 35392, Giessen, Germany. Till.F.Schaeberle@agrar.uni-giessen.de.ORCID http://orcid.org/0000-0001-9947-8079
Stéphane HacquardDepartment of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, 50829, Cologne, Germany. hacquard@mpipz.mpg.de.ORCID http://orcid.org/0000-0003-2293-3525

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) MICRORULES
6 · The paper itself

Abstract

Various microbes isolated from healthy plants are detrimental under laboratory conditions, indicating the existence of molecular mechanisms preventing disease in nature. Here, we demonstrated that application of sodium chloride (NaCl) in natural and gnotobiotic soil systems is sufficient to induce plant disease caused by an otherwise non-pathogenic root-derived Pseudomonas brassicacearum isolate (R401). Disease caused by combinatorial treatment of NaCl and R401 triggered extensive, root-specific transcriptional reprogramming that did not involve down-regulation of host innate immune genes, nor dampening of ROS-mediated immunity. Instead, we identified and structurally characterized the R401 lipopeptide brassicapeptin A as necessary and sufficient to promote disease on salt-treated plants. Brassicapeptin A production is salt-inducible, promotes root colonization and transitions R401 from being beneficial to being detrimental on salt-treated plants by disturbing host ion homeostasis, thereby bolstering susceptibility to osmolytes. We conclude that the interaction between a global change stressor and a single exometabolite from a member of the root microbiome promotes plant disease in complex soil systems.

Indexed as

Osmotic PressurePlant DiseasesPlant RootsPseudomonasArabidopsisLipopeptidesSodium ChlorideSoil MicrobiologyLipopeptidesSodium Chloride

Identifiers

PMID38806462
PMCPMC11133316

What OpenQuestion holds

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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.