Evidence map›Paper›PMID 20545853›Full record

ArticleMolecular microbiology2010

The Actinomyces oris type 2 fimbrial shaft FimA mediates co-aggregation with oral streptococci, adherence to red blood cells and biofilm development.

Arunima Mishra, Chenggang Wu, Jinghua Yang, John O Cisar, Asis Das, Hung Ton-That

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.4field-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

56 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. Article
  3. Functional Characterization of a Putative Sortase FA1364 inInternational journal of molecular sciences · 2026
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  5. Review
  6. Identifying essential genes inJournal of bacteriology · 2025
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  9. Article
  10. Single-Copy Gene Editing of a Cell Wall-Anchored Pilin in Actinomyces oris.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. The Pathogenic Role ofAntibiotics (Basel, Switzerland) · 2020
    Review
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Arunima MishraDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
Chenggang WuDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
Jinghua YangDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
John O CisarDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
Asis DasDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
Hung Ton-ThatDepartment of Microbiology & Molecular Genetics, University of Texas Health Science Center, Houston, TX, USAOral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USADepartment of Molecular, Microbial & Structural Biology, University of Connecticut Health Center, Farmington, CT, USA.
The University of Texas Health Science Center at Houston · USNational Institutes of Health · USUConn Health · US

Funding

Molecular Biology of Oral Microbial Adhesins and ReceptorsZIADE000672 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI CISAR, JOHN O · 2009 to 2016
$6.9M
Molecular Assembly on the Cell Surface of ActinomycesR01DE017382 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Hung Ton-That · 2008 to 2026
$6.7M
Intramural NIH HHSNIDCR NIH HHS DE017382NIDCR NIH HHS R01 DE017382
6 · The paper itself

Abstract

Interbacterial interactions between oral streptococci and actinomyces and their adherence to tooth surface and the associated host cells are key early events that promote development of the complex oral biofilm referred to as dental plaque. These interactions depend largely on a lectin-like activity associated with the Actinomyces oris type 2 fimbria, a surface structure assembled by sortase (SrtC2)-dependent polymerization of the shaft and tip fimbrillins, FimA and FimB respectively. To dissect the function of specific fimbrillins in various adherence processes, we have developed a convenient new technology for generating unmarked deletion mutants of A. oris. Here, we show that the fimB mutant, which produced type 2 fimbriae composed only of FimA, like the wild type co-aggregated strongly with receptor-bearing streptococci, agglutinated with sialidase-treated red blood cells, and formed monospecies biofilm. In contrast, the fimA and srtC2 mutants lacked type 2 fimbriae and were non-adherent in each of these assays. Plasmid-based expression of the deleted gene in respective mutants restored adherence to wild-type levels. These findings uncover the importance of the lectin-like activity of the polymeric FimA shaft rather than the tip. The multivalent adhesive function of FimA makes it an ideal molecule for exploring novel intervention strategies to control plaque biofilm formation.

Indexed as

Bacterial AdhesionMicrobial InteractionsActinomycesBiofilmsErythrocytesFimbriae ProteinsGene DeletionGenetic Complementation TestStreptococcusFimbriae Proteinsfimbrillin

Identifiers

PMID20545853
PMCPMC2946971
OpenAlexW1889411805

What OpenQuestion holds

Textmetadata
LicenceTDM
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.