Evidence map›Paper›PMID 27199346›Full record

ArticleFEMS microbiology ecology2016

Role of secondary metabolites in the interaction between Pseudomonas fluorescens and soil microorganisms under iron-limited conditions.

Aurélie Deveau, Harald Gross, Béatrice Palin, Samina Mehnaz, Max Schnepf, Pierre Leblond, Pieter C Dorrestein, Bertrand Aigle

Open access · bronzeAbstract read
In one paragraph

Article in FEMS microbiology ecology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
13.0field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 64 citations in OpenAlex.

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  15. Multiple siderophores: bug or feature?Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2018
    Review
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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 at 6 institutions in 4 countries.

Aurélie DeveauINRA, Interactions Arbres-Microorganismes, UMR1136, Université de Lorraine, F-54280 Champenoux, France deveau@nancy.inra.fr.
Harald GrossDepartment of Pharmaceutical Biology, Pharmaceutical Institute, University of Tuebingen, Auf der Morgenstelle 8, 72076 Tuebingen, Germany.
Béatrice PalinINRA, Interactions Arbres-Microorganismes, UMR1136, Université de Lorraine, F-54280 Champenoux, France.
Samina MehnazDepartment of Pharmaceutical Biology, Pharmaceutical Institute, University of Tuebingen, Auf der Morgenstelle 8, 72076 Tuebingen, Germany Department of Biological Sciences, Forman Christian College, Ferozepur Road, Lahore 54600, Pakistan.
Max SchnepfDepartment of Pharmaceutical Biology, Pharmaceutical Institute, University of Tuebingen, Auf der Morgenstelle 8, 72076 Tuebingen, Germany.
Pierre LeblondDynamique des Génomes et Adaptation Microbienne, UMR1128, Université de Lorraine, Faculté des Sciences et Technologies-Campus Aiguillettes, Vandœuvre-lès-Nancy, F-54506, France.
Pieter C DorresteinCollaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, CA 92093, USA.
Bertrand AigleDynamique des Génomes et Adaptation Microbienne, UMR1128, Université de Lorraine, Faculté des Sciences et Technologies-Campus Aiguillettes, Vandœuvre-lès-Nancy, F-54506, France.
Université de Lorraine · FRUniversity of Tübingen · DEDynamique des Génomes et Adaptation Microbienne · FRForman Christian College · PKInteractions Arbres-Microorganismes · FRUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microorganisms can be versatile in their interactions with each other, being variously beneficial, neutral or antagonistic in their effect. Although this versatility has been observed among many microorganisms and in many environments, little is known regarding the mechanisms leading to these changes in behavior. In the present work, we analyzed the mechanism by which the soil bacterium Pseudomonas fluorescens BBc6R8 shifts from stimulating the growth of the ectomycorrhizal fungus Laccaria bicolor S238N to killing the fungus. We show that among the three secondary metabolites produced by the bacterial strain-the siderophores enantio-pyochelin and pyoverdine, and the biosurfactant viscosin-the siderophores are mainly responsible for the antagonistic activity of the bacterium under iron-limited conditions. While the bacterial strain continues to produce beneficial factors, their effects are overridden by the action of their siderophores. This antagonistic activity of the strain P. fluorescens BBC6R8 in iron-depleted environments is not restricted to its influence on L. bicolor, since it was also seen to inhibit the growth of the actinomycete Streptomyces ambofaciens ATCC23877. We show that the strain P. fluorescens BBc6R8 uses different strategies to acquire iron, depending on certain biotic and abiotic factors.

Indexed as

Soil MicrobiologyIronMycorrhizaeOligopeptidesPhenolsPseudomonas fluorescensSiderophoresSoilStreptomycesThiazolesIronOligopeptidesPhenolspyochelinpyoverdinSiderophoresSoilThiazolesantagonismironmutualismmycorrhiza helper bacteriasiderophoresviscosin

Identifiers

PMID27199346
PMCPMC5975829
OpenAlexW2401820765

What OpenQuestion holds

Textmetadata
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.