Evidence map›Paper›PMID 33522633›Full record

ArticleThe EMBO journal2021

Bacterial protein domains with a novel Ig-like fold target human CEACAM receptors.

Nina M van Sorge, Daniel A Bonsor, Liwen Deng, Erik Lindahl, Verena Schmitt, Mykola Lyndin, Alexej Schmidt, Olof R Nilsson, Jaime Brizuela, Elena Boero and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 33 citations in OpenAlex.

  1. The role of adhesins ofGut microbes · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Neutrophil CEACAMs and the Inflammatory Response toJournal of innate immunity · 2026
    Review
  7. Article
  8. Article
  9. Binding ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Structural basis for immune cell binding ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Evolution of CEACAM pathogen decoy receptors in primates.European journal of clinical investigation · 2024
    Article
  14. Structural aspects of CEACAM1 interactions.European journal of clinical investigation · 2024
    Review
  15. Article
  16. The role of CEACAMs in neutrophil function.European journal of clinical investigation · 2024
    Review
  17. Review
  18. Tethering of soluble immune effectors to mucin and chitin reflects a convergent and dynamic role in gut immunity.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  19. Metagenome-assembled genomes of threeAccess microbiology · 2024
    Article
  20. Lactobacilli-host interactions inhibitFrontiers in microbiology · 2024
    Article
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

16 authors at 9 institutions in 6 countries.

Nina M van SorgeDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-2695-5863
Daniel A BonsorInstitute of Human Virology, University of Maryland School of Medicine, University of Maryland, Baltimore, MD, USA.ORCID 0000-0001-5746-6002
Liwen DengDepartment of Immunology & Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0002-7984-8471
Erik LindahlDepartment of Biochemistry and Biophysics, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.ORCID 0000-0002-2734-2794
Verena SchmittInstitute of Anatomy, Medical Faculty, University Duisburg-Essen, Essen, Germany.ORCID 0000-0002-6951-6406
Mykola LyndinInstitute of Anatomy, Medical Faculty, University Duisburg-Essen, Essen, Germany.ORCID 0000-0003-4385-3903
Alexej SchmidtDepartment of Medical Biosciences, Umeå University, Pathology, Umeå, Sweden.ORCID 0000-0001-7155-8667
Olof R NilssonDepartment of Laboratory Medicine, Division of Medical Microbiology, Lund University, Lund, Sweden.
Jaime BrizuelaDepartment of Infectious Disease, MRC Centre for Molecular Bacteriology & Infection, Imperial College London, London, UK.
Elena BoeroDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Eric J SundbergInstitute of Human Virology, University of Maryland School of Medicine, University of Maryland, Baltimore, MD, USA.ORCID 0000-0003-0478-3033
Jos A G van StrijpDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0001-6253-0830
Kelly S DoranDepartment of Immunology & Microbiology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0003-4232-6837
Bernhard B SingerInstitute of Anatomy, Medical Faculty, University Duisburg-Essen, Essen, Germany.ORCID 0000-0002-2213-6000
Gunnar LindahlDepartment of Laboratory Medicine, Division of Medical Microbiology, Lund University, Lund, Sweden.ORCID 0000-0002-5734-1864
Alex J McCarthyDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-4105-3737
Utrecht University · NLLund University · SEUniversity of Colorado Anschutz Medical Campus · USUniversity of Duisburg-Essen · DEUniversity of Maryland, Baltimore · USImperial College London · GBStockholm University · SESumy State University · UAUmeå University · SE

Funding

Modulation of Blood-Brain Barrier Defense and Dysfunction during Bacterial MeningitisR01NS116716 · NINDS · UNIVERSITY OF COLORADO DENVER · PI DORAN, KELLY S · 2020 to 2024
$1.9M
Medical Research Council MR/P028225/1NINDS NIH HHS R01 NS116716
6 · The paper itself

Abstract

Streptococcus agalactiae, also known as group B Streptococcus (GBS), is the major cause of neonatal sepsis in humans. A critical step to infection is adhesion of bacteria to epithelial surfaces. GBS adhesins have been identified to bind extracellular matrix components and cellular receptors. However, several putative adhesins have no host binding partner characterised. We report here that surface-expressed β protein of GBS binds to human CEACAM1 and CEACAM5 receptors. A crystal structure of the complex showed that an IgSF domain in β represents a novel Ig-fold subtype called IgI3, in which unique features allow binding to CEACAM1. Bioinformatic assessment revealed that this newly identified IgI3 fold is not exclusively present in GBS but is predicted to be present in adhesins from other clinically important human pathogens. In agreement with this prediction, we found that CEACAM1 binds to an IgI3 domain found in an adhesin from a different streptococcal species. Overall, our results indicate that the IgI3 fold could provide a broadly applied mechanism for bacteria to target CEACAMs.

Indexed as

Adhesins, BacterialAnimalsAntigens, CDBinding SitesCarcinoembryonic AntigenCell Adhesion MoleculesCHO CellsCricetinaeCricetulusGPI-Linked ProteinsHeLa CellsHumansProtein BindingStreptococcus agalactiaeAdhesins, BacterialAntigens, CDCarcinoembryonic AntigenCD66 antigensCEACAM5 protein, humanCell Adhesion MoleculesGPI-Linked ProteinsAdhesinIgIimmunoglobulin superfamilyreceptorStreptococcus agalactiae

Identifiers

PMID33522633
PMCPMC8013792
OpenAlexW3127713179

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.