Evidence map›Paper›PMID 25024364›Full record

ArticleInfection and immunity2014

Aggregatibacter actinomycetemcomitans outer membrane vesicles are internalized in human host cells and trigger NOD1- and NOD2-dependent NF-κB activation.

Bernard Thay, Anna Damm, Thomas A Kufer, Sun Nyunt Wai, Jan Oscarsson

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

87 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  4. Fimbriae potentiateCurrent research in microbial sciences · 2026
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  5. The role ofJournal of oral microbiology · 2026
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  6. Article
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  8. Journal of oral microbiology · 2025
    Article
  9. Pattern Recognition by NOD-Like Receptors.Advances in experimental medicine and biology · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Frontiers in immunology · 2024
    Review
  18. Review
  19. Review
  20. Article

27 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Bernard ThayOral Microbiology, Department of Odontology, Umeå University, Umeå, Sweden.
Anna DammInstitute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany.
Thomas A KuferInstitute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Cologne, Germany.
Sun Nyunt WaiDepartment of Molecular Biology and Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden.
Jan OscarssonOral Microbiology, Department of Odontology, Umeå University, Umeå, Sweden jan.oscarsson@odont.umu.se.
Umeå University · SEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aggregatibacter actinomycetemcomitans is an oral and systemic pathogen associated with aggressive forms of periodontitis and with endocarditis. We recently demonstrated that outer membrane vesicles (OMVs) disseminated by A. actinomycetemcomitans could deliver multiple proteins, including biologically active cytolethal distending toxin (CDT), into the cytosol of HeLa cells and human gingival fibroblasts (HGF). In the present work, we have used immunoelectron and confocal microscopy analysis and fluorescently labeled vesicles to further investigate mechanisms for A. actinomycetemcomitans OMV-mediated delivery of bacterial antigens to these host cells. Our results supported that OMVs were internalized into the perinuclear region of HeLa cells and HGF. Colocalization analysis revealed that internalized OMVs colocalized with the endoplasmic reticulum and carried antigens, detected using an antibody specific to whole A. actinomycetemcomitans serotype a cells. Consistent with OMV internalization mediating intracellular antigen exposure, the vesicles acted as strong inducers of cytoplasmic peptidoglycan sensor NOD1- and NOD2-dependent NF-κB activation in human embryonic kidney cells. Moreover, NOD1 was the main sensor of OMV-delivered peptidoglycan in myeloid THP1 cells, contributing to the overall inflammatory responses induced by the vesicles. This work reveals a role of A. actinomycetemcomitans OMVs as a trigger of innate immunity via carriage of NOD1- and NOD2-active pathogen-associated molecular patterns (PAMPs).

Indexed as

EndocytosisAggregatibacter actinomycetemcomitansAntigens, BacterialBacterial ProteinsCell LineEpithelial CellsFibroblastsHost-Pathogen InteractionsHumansMicroscopy, ConfocalMicroscopy, ImmunoelectronNF-kappa BNod1 Signaling Adaptor ProteinNod2 Signaling Adaptor ProteinSecretory VesiclesAntigens, BacterialBacterial ProteinsNF-kappa BNOD1 protein, humanNod1 Signaling Adaptor ProteinNOD2 protein, humanNod2 Signaling Adaptor Protein

Identifiers

PMID25024364
PMCPMC4187862
OpenAlexW2096448430

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.