Evidence map›Paper›PMID 28382776›Full record

ArticleMolecular oral microbiology2017

Behavior of two Tannerella forsythia strains and their cell surface mutants in multispecies oral biofilms.

Susanne Bloch, Thomas Thurnheer, Yukitaka Murakami, Georgios N Belibasakis, Christina Schäffer

Open access · hybridAbstract read
In one paragraph

Article in Molecular oral microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Obtaining Muramic Acid fromLife (Basel, Switzerland) · 2025
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  6. Advances in the type IX secretion system: an exploration focusing onCurrent research in microbial sciences · 2025
    Review
  7. Article
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  9. The intriguing strategies ofFrontiers in oral health · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Journal of oral microbiology · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Characterization ofMicrobiology (Reading, England) · 2019
    Article
  19. Review
  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

5 authors at 3 institutions in 3 countries.

Susanne BlochDepartment of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Vienna, Vienna, Austria.
Thomas ThurnheerDivision of Oral Microbiology and Immunology, Institute of Oral Biology, Center of Dental Medicine, University of Zürich, Zürich, Switzerland.
Yukitaka MurakamiDepartment of Oral Microbiology, Asahi University School of Dentistry, Mizuho, Gifu, Japan.
Georgios N BelibasakisDivision of Cariology and Endodontics, Department of Dental Medicine, Karolinska Institute, Huddinge, Sweden.
Christina SchäfferDepartment of NanoBiotechnology, NanoGlycobiology unit, Universität für Bodenkultur Vienna, Vienna, Austria.ORCID 0000-0003-1613-7258
Asahi University · JPKarolinska Institutet · SEUniversity of Zurich · CH

Funding

Austrian Science Fund FWF P 24317Austrian Science Fund FWF P 26836Austrian Science Fund FWF W 1224
6 · The paper itself

Abstract

As a member of subgingival multispecies biofilms, Tannerella forsythia is commonly associated with periodontitis. The bacterium has a characteristic cell surface (S-) layer modified with a unique O-glycan. Both the S-layer and the O-glycan were analyzed in this study for their role in biofilm formation by employing an in vitro multispecies biofilm model mimicking the situation in the oral cavity. Different T. forsythia strains and mutants with characterized defects in cell surface composition were incorporated into the model, together with nine species of select oral bacteria. The influence of the T. forsythia S-layer and attached glycan on the bacterial composition of the biofilms was analyzed quantitatively using colony-forming unit counts and quantitative real-time polymerase chain reaction, as well as qualitatively by fluorescence in situ hybridization and confocal laser scanning microscopy. This revealed that changes in the T. forsythia cell surface did not affect the quantitative composition of the multispecies consortium, with the exception of Campylobacter rectus cell numbers. The localization of T. forsythia within the bacterial agglomeration varied depending on changes in the S-layer glycan, and this also affected its aggregation with Porphyromonas gingivalis. This suggests a selective role for the glycosylated T. forsythia S-layer in the positioning of this species within the biofilm, its co-localization with P. gingivalis, and the prevalence of C. rectus. These findings might translate into a potential role of T. forsythia cell surface structures in the virulence of this species when interacting with host tissues and the immune system, from within or beyond the biofilm.

Indexed as

BiofilmsMutationCampylobacter rectusCell MembraneGingivaGlycosylationMicrobial InteractionsMouthPeriodontal DiseasesPeriodontitisPorphyromonas gingivalisPrevotella intermediaReal-Time Polymerase Chain ReactionTannerella forsythiaTreponema denticolaVirulenceCampylobacter rectuscell surfaceoral biofilmperiodontal diseaseS-layer glycosylationTannerella forsythia

Identifiers

PMID28382776
PMCPMC5600126
OpenAlexW2604228488

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.