Evidence map›Paper›PMID 18723678›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Role of glycan synthesis in colonization of the mammalian gut by the bacterial symbiont Bacteroides fragilis.

Michael J Coyne, Maria Chatzidaki-Livanis, Lawrence C Paoletti, Laurie E Comstock

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.6field-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

65 citing papers in PubMed, 109 citations in OpenAlex.

  1. Trial
  2. Comparative genomic analysis ofMicrobiology spectrum · 2026
    Article
  3. Article
  4. Article
  5. Stepwise Assembly of theBiochemistry · 2026
    Article
  6. Gene regulation inMicrobiology and molecular biology reviews : MMBR · 2025
    Review
  7. Review
  8. Article
  9. Role of phase-variable Mfa1 fimbriae ofGut microbes reports · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

5 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

4 authors at 2 institutions in 1 country.

Michael J CoyneChanning Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Maria Chatzidaki-Livanis
Lawrence C Paoletti
Laurie E Comstock
Brigham and Women's Hospital · USHarvard University · US

Funding

Regulation of the multiple polysaccharides of Bacteroides fragilisR01AI044193 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI COMSTOCK, LAURIE E · 1999 to 2010
$2.7M
Genetic Basis of Abscess Formation by B. fragilisR01AI053694 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI COMSTOCK, LAURIE E · 2003 to 2006
$975k
Regulation of the multiple polysaccharides of Bacteroides fragilisR56AI044193 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI COMSTOCK, LAURIE E · 2008 to 2008
$344k
NIAID NIH HHS AI044193NIAID NIH HHS AI053694NIAID NIH HHS R01 AI044193NIAID NIH HHS R01 AI053694NIAID NIH HHS R56 AI044193
6 · The paper itself

Abstract

Bacteroides species are the most abundant Gram-negative bacteria of the human colonic microbiota. These endogenous organisms are unique in that they synthesize an extensive number of phase-variable surface polysaccharides. Pathogenic bacteria phase vary expression of surface molecules for immune evasion, but the importance of the synthesis of multiple phase-variable polysaccharides to these commensal bacteria is unknown. We previously showed that a Bacteroides fragilis mutant unable to synthesize 4 of the 8 capsular polysaccharides and unable to glycosylate proteins properly is rapidly outcompeted by the wild-type strain for colonization of the gnotobiotic mouse intestine. In the present study, we constructed mutants defective only in capsule polysaccharide synthesis to define better the importance of these surface molecules to intestinal colonization. We discovered a key enzymatic activity required for synthesis of 7 of the 8 capsular polysaccharides. Deletion of its gene resulted in the first B. fragilis mutant able to synthesize only one phase-variable polysaccharide, and further mutation resulted in a stable acapsular mutant. We show that the acapsular mutant is rapidly outcompeted, but synthesis of a single polysaccharide is sufficient for the organism to colonize the gnotobiotic intestine competitively. These data demonstrate that initial colonization of the gnotobiotic mouse intestine by B. fragilis requires that the organism synthesize only a single polysaccharide and suggest that the synthesis of multiple phase-variable polysaccharides is important for the bacteria's long-term maintenance in the normally complex and competitive ecosystem.

Indexed as

SymbiosisAnimalsBacterial CapsulesBacterial ProteinsBacteroides fragilisBiological AssayColony Count, MicrobialFecesGastrointestinal TractGlycoproteinsMammalsMiceMicrobial ViabilityMutationPolysaccharidesBacterial ProteinsGlycoproteinsPolysaccharides

Identifiers

PMID18723678
PMCPMC2529095
OpenAlexW2022338512

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.