Evidence map›Paper›PMID 32516311›Full record

ArticlePLoS biology2020

Modulation of bacterial multicellularity via spatio-specific polysaccharide secretion.

Salim T Islam, Israel Vergara Alvarez, Fares Saïdi, Annick Guiseppi, Evgeny Vinogradov, Gaurav Sharma, Leon Espinosa, Castrese Morrone, Gael Brasseur, Jean-François Guillemot and 9 more

Abstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
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  7. Milestones in the development ofJournal of bacteriology · 2025
    Review
  8. Article
  9. Applied and environmental microbiology · 2024
    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

19 authors.

Salim T IslamArmand Frappier Health & Biotechnology Research Centre, Institut National de la Recherche Scientifique, Université du Québec, Institut Pasteur International Network, Laval, Québec, Canada.ORCID 0000-0001-6853-8446
Israel Vergara AlvarezLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.ORCID 0000-0002-3070-5365
Fares SaïdiArmand Frappier Health & Biotechnology Research Centre, Institut National de la Recherche Scientifique, Université du Québec, Institut Pasteur International Network, Laval, Québec, Canada.
Annick GuiseppiLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.
Evgeny VinogradovHuman Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.ORCID 0000-0002-5364-1376
Gaurav SharmaDepartment of Microbiology and Molecular Genetics, University of California-Davis, Davis, California, United States of America.ORCID 0000-0002-2861-7446
Leon EspinosaLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.ORCID 0000-0002-1923-2069
Castrese MorroneLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.
Gael BrasseurLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.
Jean-François GuillemotCNRS-Institut de Microbiologie de la Méditerranée, Marseille, France.
Anaïs BenaroucheTeclis Scientific, Civrieux d'Azergue, France.
Jean-Luc BridotTeclis Scientific, Civrieux d'Azergue, France.
Gokulakrishnan RavicoularaminArmand Frappier Health & Biotechnology Research Centre, Institut National de la Recherche Scientifique, Université du Québec, Institut Pasteur International Network, Laval, Québec, Canada.
Alain CagnaTeclis Scientific, Civrieux d'Azergue, France.
Charles GauthierArmand Frappier Health & Biotechnology Research Centre, Institut National de la Recherche Scientifique, Université du Québec, Institut Pasteur International Network, Laval, Québec, Canada.ORCID 0000-0002-2475-2050
Mitchell SingerDepartment of Microbiology and Molecular Genetics, University of California-Davis, Davis, California, United States of America.ORCID 0000-0001-6356-0863
Henri-Pierre FierobeLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.
Tâm MignotLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.ORCID 0000-0003-4338-9063
Emilia M F MaurielloLaboratoire de Chimie Bactérienne, CNRS-Université Aix-Marseille UMR, Institut de Microbiologie de la Méditerranée, Marseille, France.ORCID 0000-0001-9770-6138

Funding

CIHR 321028
6 · The paper itself

Abstract

The development of multicellularity is a key evolutionary transition allowing for differentiation of physiological functions across a cell population that confers survival benefits; among unicellular bacteria, this can lead to complex developmental behaviors and the formation of higher-order community structures. Herein, we demonstrate that in the social δ-proteobacterium Myxococcus xanthus, the secretion of a novel biosurfactant polysaccharide (BPS) is spatially modulated within communities, mediating swarm migration as well as the formation of multicellular swarm biofilms and fruiting bodies. BPS is a type IV pilus (T4P)-inhibited acidic polymer built of randomly acetylated β-linked tetrasaccharide repeats. Both BPS and exopolysaccharide (EPS) are produced by dedicated Wzx/Wzy-dependent polysaccharide-assembly pathways distinct from that responsible for spore-coat assembly. While EPS is preferentially produced at the lower-density swarm periphery, BPS production is favored in the higher-density swarm interior; this is consistent with the former being known to stimulate T4P retraction needed for community expansion and a function for the latter in promoting initial cell dispersal. Together, these data reveal the central role of secreted polysaccharides in the intricate behaviors coordinating bacterial multicellularity.

Indexed as

AcetylationBiosynthetic PathwaysCarbon-13 Magnetic Resonance SpectroscopyCell MembraneMultigene FamilyMyxococcus xanthusPolysaccharides, BacterialProton Magnetic Resonance SpectroscopySurface-Active AgentsPolysaccharides, BacterialSurface-Active Agents

Identifiers

PMID32516311
PMCPMC7310880

What OpenQuestion holds

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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.