Evidence map›Paper›PMID 22539957›Full record

ArticlePloS one2012

Quorum sensing signaling molecules produced by reference and emerging soft-rot bacteria (Dickeya and Pectobacterium spp.).

Alexandre Crépin, Corinne Barbey, Amélie Beury-Cirou, Valérie Hélias, Laure Taupin, Sylvie Reverchon, William Nasser, Denis Faure, Alain Dufour, Nicole Orange and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. 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
3.2field-weighted citation impact, top 7% 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, 59 citations in OpenAlex.

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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

14 authors at 7 institutions in 3 countries.

Alexandre CrépinLaboratoire de Microbiologie Signaux et Microenvironnement, Normandie Université, Université de Rouen EA 4312, IUT, Evreux, Evreux, France.
Corinne Barbey
Amélie Beury-Cirou
Valérie Hélias
Laure Taupin
Sylvie Reverchon
William Nasser
Denis Faure
Alain Dufour
Nicole Orange
Marc Feuilloley
Karin Heurlier
Jean-François Burini
Xavier Latour
Centre National de la Recherche Scientifique · FRNormandie Université · FRUniversité de Rouen Normandie · FRUniversité de Bretagne Sud · FRInstitut National de la Recherche Agronomique · MAUniversité Claude Bernard Lyon 1 · FRUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral small diffusible molecules are involved in bacterial quorum sensing and virulence. The production of autoinducers-1 and -2, quinolone, indole and γ-amino butyrate signaling molecules was investigated in a set of soft-rot bacteria belonging to six Dickeya or Pectobacterium species including recent or emerging potato isolates. METHODOLOGY/PRINCIPAL

findingsUsing bacterial biosensors, immunoassay, and chromatographic analysis, we showed that soft-rot bacteria have the common ability to produce transiently during their exponential phase of growth the N-3-oxo-hexanoyl- or the N-3-oxo-octanoyl-l-homoserine lactones and a molecule of the autoinducer-2 family. Dickeya spp. produced in addition the indole-3-acetic acid in tryptophan-rich conditions. All these signaling molecules have been identified for the first time in the novel Dickeya solani species. In contrast, quinolone and γ-amino butyrate signals were not identified and the corresponding synthases are not present in the available genomes of soft-rot bacteria. To determine if the variations of signal production according to growth phase could result from expression modifications of the corresponding synthase gene, the respective mRNA levels were estimated by reverse transcriptase-PCR. While the N-acyl-homoserine lactone production is systematically correlated to the synthase expression, that of the autoinducer-2 follows the expression of an enzyme upstream in the activated methyl cycle and providing its precursor, rather than the expression of its own synthase. CONCLUSIONS/SIGNIFICANCE: Despite sharing the S-adenosylmethionine precursor, no strong link was detected between the production kinetics or metabolic pathways of autoinducers-1 and -2. In contrast, the signaling pathway of autoinducer-2 seems to be switched off by the indole-3-acetic acid pathway under tryptophan control. It therefore appears that the two genera of soft-rot bacteria have similarities but also differences in the mechanisms of communication via the diffusible molecules. Our results designate autoinducer-1 lactones as the main targets for a global biocontrol of soft-rot bacteria communications, including those of emerging isolates.

Indexed as

Quorum Sensing4-ButyrolactoneAcyl-ButyrolactonesBacterial ProteinsEnterobacteriaceaegamma-Aminobutyric AcidHomoserineIndoleacetic AcidsKineticsLactonesMultienzyme ComplexesPectobacteriumQuinolonesRNA, MessengerSignal TransductionSolanum tuberosum4-ButyrolactoneAcyl-ButyrolactonesBacterial Proteinsgamma-Aminobutyric AcidHomoserineindole-3-acetic acid synthaseindoleacetic acidIndoleacetic AcidsLactonesMultienzyme ComplexesN-(3-oxohexanoyl)-3-aminodihydro-2(3H)-furanoneN-octanoylhomoserine lactoneQuinolonesRNA, MessengerTryptophan

Identifiers

PMID22539957
PMCPMC3335102
OpenAlexW2066275510

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.