Evidence map›Paper›PMID 42467739›Full record

ArticlePLoS pathogens2026

Auxin biosynthesis and signaling drive virulence and plant adaptation in Dickeya dadantii.

Amalia Roca, Saray Santamaría-Hernando, Zulema Udaondo, Juan J Cabrera, Patricia Godoy, Ana Nogueira, Emilia López-Solanilla, Miguel A Matilla

Abstract read
In one paragraph

Article in PLoS pathogens, 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
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0citing papers in PubMed
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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

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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

8 authors.

Amalia RocaDepartment of Microbiology, Facultad de Farmacia, Campus Universitario de Cartuja, Universidad de Granada, Granada, Spain.
Saray Santamaría-HernandoCentro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM)-Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA-CSIC), Pozuelo de Alarcón, Madrid, Spain.
Zulema UdaondoDepartment of Microbial Biotechnology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Juan J CabreraDepartment of Biotechnology and Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.
Patricia GodoyDepartment of Biotechnology and Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.
Ana NogueiraDepartment of Biotechnology and Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.
Emilia López-SolanillaCentro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM)-Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA-CSIC), Pozuelo de Alarcón, Madrid, Spain.
Miguel A MatillaDepartment of Biotechnology and Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.ORCID 0000-0002-8468-9604

Funding

Innovation and Universities/Agencia Estatal de InvestigaciónSpanish Ministry for Science
6 · The paper itself

Abstract

Plants and their associated bacteria engage in complex bidirectional interactions mediated by a diverse array of signaling molecules of both plant and microbial origin. Indole-3-acetic acid (IAA) is a central phytohormone regulating plant growth and development and is increasingly recognized as an intra- and inter-kingdom signaling molecule that modulates diverse bacterial processes relevant during plant-microbe interactions. While IAA biosynthesis is widespread among plant-associated bacteria, the mechanisms through which this auxin regulates bacterial physiology and virulence, as well as those controlling its production, remain poorly understood. Here, we show that IAA synthesis deficiency in the global phytopathogen Dickeya dadantii triggers transcriptional reprogramming and results in reduced virulence and fitness during plant infection. Endogenous IAA was found to regulate the expression of the AaeXAB efflux pump, which mediates endogenous IAA secretion, confers resistance to plant defense-related phytohormones, and contributes to plant virulence in D. dadantii. Consistent with its role in plant-bacteria interactions, phylogenetic analyses revealed that AaeXAB-encoding genes are commonly present among Pseudomonadota isolated from plant-associated environments. Moreover, IAA deficiency altered the expression of a previously uncharacterized indole-responsive MarR-type regulator, DDA3937_RS07305, suggesting cross-talk between IAA- and indole-mediated signaling networks. Our data also uncover a complex regulatory circuit coordinating IAA production in D. dadantii, involving the ExpIR and Vfm quorum-sensing systems and the transcriptional regulators TyrR, TrpR, and LrhA. Collectively, our findings provide new insights into the role of IAA as a bacterial signal promoting plant adaptation and virulence. Targeting IAA biosynthesis and efflux pump activity may offer promising avenues for the development of anti-virulence strategies in phytopathogenesis.

Indexed as

DickeyaIndoleacetic AcidsPlant DiseasesAdaptation, PhysiologicalBacterial ProteinsGene Expression Regulation, BacterialPlant Growth RegulatorsSignal TransductionVirulenceBacterial Proteinsindoleacetic acidIndoleacetic AcidsPlant Growth Regulators

Identifiers

PMID42467739
PMCPMC13395407

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LicenceCC BY
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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 OpenQuestion graph.