Evidence map›Paper›PMID 25800812›Full record

ReviewCurrent genetics2015

Cyclic-di-GMP signaling in the Gram-positive pathogen Clostridium difficile.

Eric Bordeleau, Vincent Burrus

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Cyclic-di-GMP regulation of virulence in bacterial pathogens.Wiley interdisciplinary reviews. RNA · 2018
    Review
  6. Article
  7. Review
  8. Review
  9. Clostridium difficile infection.Nature reviews. Disease primers · 2016
    Review
  10. Review
  11. Review
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

2 authors at 1 institution in 1 country.

Eric BordeleauDépartement de biologie, Faculté des sciences, Université de Sherbrooke, Quebec, Canada. eric.bordeleau@usherbrooke.ca.
Vincent BurrusDépartement de biologie, Faculté des sciences, Université de Sherbrooke, Quebec, Canada.
Université de Sherbrooke · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anaerobic Gram-positive bacterium Clostridium difficile causes intestinal infections responsible for symptoms ranging from mild diarrhea to fulminant colitis. Like other bacteria, C. difficile needs to sense and integrate environmental signals in order to adapt to changes and thrive in its environment. The second messenger cyclic diguanosine monophosphate (c-di-GMP) was recently recognized as a quasi-ubiquitous phenotype coordinator in bacteria. Mostly known to be involved in the transition from motile to sessile and multicellular behaviors in Gammaproteobacteria, c-di-GMP is now known to regulate many other phenotypes from cell morphogenesis to virulence, in many Gram-negative and a few Gram-positive bacteria. Herein, we review recent advances in our understanding of c-di-GMP signaling in the lifecycle of C. difficile.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsBacterial ToxinsBiofilmsClostridioides difficileCyclic GMPEnterotoxinsPhenotypeRiboswitchSecond Messenger SystemsVirulenceBacterial ProteinsBacterial Toxinsbis(3',5')-cyclic diguanylic acidCyclic GMPEnterotoxinsRiboswitchtcdA protein, Clostridium difficiletoxB protein, Clostridium difficileBiofilmClostridium difficileCyclic-di-GMPMotilityRiboswitchToxins

Identifiers

PMID25800812
OpenAlexW2023479978

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.