Evidence map›Paper›PMID 31367003›Full record

ArticleScientific reports2019

Differential homotypic and heterotypic interactions of antigen 43 (Ag43) variants in autotransporter-mediated bacterial autoaggregation.

Valentin Ageorges, Marion Schiavone, Grégory Jubelin, Nelly Caccia, Philippe Ruiz, Ingrid Chafsey, Xavier Bailly, Etienne Dague, Sabine Leroy, Jason Paxman and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
2.1field-weighted citation impact, top 15% 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, 29 citations in OpenAlex.

  1. Antigen 43 associated withMicrobiology spectrum · 2025
    Article
  2. Review
  3. Article
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  5. The non-attached biofilm aggregate.Communications biology · 2023
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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

15 authors at 6 institutions in 4 countries.

Valentin AgeorgesUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Marion SchiavoneLallemand Animal Nutrition, 31702, Blagnac, Cedex, France.
Grégory JubelinUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Nelly CacciaUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Philippe RuizUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-5149-9775
Ingrid ChafseyUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Xavier BaillyINRA UR346 Epidémiologie Animale, 63122, Saint Genès Champanelle, France.ORCID http://orcid.org/0000-0001-6959-7974
Etienne DagueLAAS-CNRS, Université de Toulouse, 31077, Toulouse, Cedex, France.
Sabine LeroyUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Jason PaxmanDepartment of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Bundoora, Victoria, 3086, Australia.ORCID http://orcid.org/0000-0002-1418-5910
Begoña HerasDepartment of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Bundoora, Victoria, 3086, Australia.
Frédérique Chaucheyras-DurandUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France.
Amanda E RossiterInstitute of Microbiology and Infection, University of Birmingham, B152TT, Birmingham, United Kingdom.
Ian R HendersonInstitute of Microbiology and Infection, University of Birmingham, B152TT, Birmingham, United Kingdom.
Mickaël DesvauxUniversité Clermont Auvergne, INRA, UMR454 MEDiS, 63000, Clermont-Ferrand, France. mickael.desvaux@inra.fr.
Université Clermont Auvergne · FRCentre National de la Recherche Scientifique · FRLa Trobe University · AUInstitut National de la Recherche Agronomique · MAThe University of Queensland · AUUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigen 43 (Ag43) is a cell-surface exposed protein of Escherichia coli secreted by the Type V, subtype a, secretion system (T5aSS) and belonging to the family of self-associating autotransporters (SAATs). These modular proteins, comprising a cleavable N-terminal signal peptide, a surface-exposed central passenger and an outer membrane C-terminal translocator, self-recognise in a Velcro-like handshake mechanism. A phylogenetic network analysis focusing on the passenger revealed for the first time that they actually distribute into four distinct classes, namely C1, C2, C3 and C4. Structural alignment and modelling analyses demonstrated these classes arose from shuffling of two different subdomains within the Ag43 passengers. Functional analyses revealed that homotypic interactions occur for all Ag43 classes but significant differences in the sedimentation kinetics and aggregation state were present when Ag43

Indexed as

Adhesins, Escherichia coliAntigenic VariationAntigens, BacterialBacterial AdhesionBacterial Outer Membrane ProteinsBiofilmsBiological TransportEscherichia coliEscherichia coli ProteinsPhylogenyType V Secretion SystemsAdhesins, Escherichia coliantigen 43, E coliAntigens, BacterialBacterial Outer Membrane ProteinsEscherichia coli ProteinsType V Secretion Systems

Identifiers

PMID31367003
PMCPMC6668479
OpenAlexW2964779058

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.