Evidence map›Paper›PMID 30500953›Full record

ArticleNucleic acids research2018

An auxin controls bacterial antibiotics production.

Miguel A Matilla, Abdelali Daddaoua, Andrea Chini, Bertrand Morel, Tino Krell

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Drug Repurposing: An Emerging Strategy inJournal of microbiology and biotechnology · 2025
    Review
  7. Indole-3-acetic acid (IAA) protectsApplied and environmental microbiology · 2025
    Article
  8. Review
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  11. 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

5 authors at 2 institutions in 1 country.

Miguel A MatillaDepartment of Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, 18008 Granada, Spain.
Abdelali Daddaoua
Andrea ChiniDepartment of Plant Molecular Genetics, National Centre for Biotechnology, Consejo Superior de Investigaciones Científicas, 28049 Madrid, Spain.
Bertrand MorelDepartament of Physical Chemistry and Institute for Biotechnology, Science Faculty, Granada University, 18071 Granada, Spain.
Tino KrellDepartment of Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, 18008 Granada, Spain.
Consejo Superior de Investigaciones Científicas · ESUniversidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of clinically used antibiotics originate from bacteria. As the need for new antibiotics grows, large-scale genome sequencing and mining approaches are being used to identify novel antibiotics. However, this task is hampered by the fact that many antibiotic biosynthetic clusters are not expressed under laboratory conditions. One strategy to overcome this limitation is the identification of signals that activate the expression of silent biosynthetic pathways. Here, we report the use of high-throughput screening to identify signals that control the biosynthesis of the acetyl-CoA carboxylase inhibitor antibiotic andrimid in the broad-range antibiotic-producing rhizobacterium Serratia plymuthica A153. We reveal that the pathway-specific transcriptional activator AdmX recognizes the auxin indole-3-acetic acid (IAA). IAA binding causes conformational changes in AdmX that result in the inhibition of the expression of the andrimid cluster and the suppression of antibiotic production. We also show that IAA synthesis by pathogenic and beneficial plant-associated bacteria inhibits andrimid production in A153. Because IAA is a signalling molecule that is present across all domains of life, this study highlights the importance of intra- and inter-kingdom signalling in the regulation of antibiotic synthesis. Our discovery unravels, for the first time, an IAA-dependent molecular mechanism for the regulation of antibiotic synthesis.

Indexed as

Gene Expression Regulation, BacterialAcetyl-CoA CarboxylaseAnti-Bacterial AgentsArabidopsisBacterial ProteinsCloning, MolecularEnzyme InhibitorsEscherichia coliGene ExpressionHigh-Throughput Screening AssaysIndoleacetic AcidsPlant RootsPlasmidsPolyenesProtein BindingPyrrolesAcetyl-CoA CarboxylaseandrimidAnti-Bacterial AgentsBacterial ProteinsEnzyme Inhibitorsindoleacetic acidIndoleacetic AcidsPolyenesPyrrolesRecombinant ProteinsTranscription Factors

Identifiers

PMID30500953
PMCPMC6265452
OpenAlexW2888245517

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.