Evidence map›Paper›PMID 24762309›Full record

ReviewFuture microbiology2014

Towards an understanding of the role of Clostridium perfringens toxins in human and animal disease.

Francisco A Uzal, John C Freedman, Archana Shrestha, James R Theoret, Jorge Garcia, Milena M Awad, Vicki Adams, Robert J Moore, Julian I Rood, Bruce A McClane

Open access · greenAbstract readReview
In one paragraph

Review in Future microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 211 papers.

0numbers the graph read from it
0cells of the map it votes in
211citing papers in PubMed
14.7field-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

211 citing papers in PubMed, 410 citations in OpenAlex.

  1. Article
  2. Review
  3. Epidemiological and Metabolic Characteristics ofAnimals : an open access journal from MDPI · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Journal of veterinary science · 2026
    Article
  10. Article
  11. A novel typing method forFrontiers in microbiology · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

151 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

10 authors at 5 institutions in 2 countries.

Francisco A UzalCalifornia Animal Health & Food Safety Laboratory System, University of California-Davis, CA, USA.
John C Freedman
Archana Shrestha
James R Theoret
Jorge Garcia
Milena M Awad
Vicki Adams
Robert J Moore
Julian I Rood
Bruce A McClane
Monash University · AUUniversity of Pittsburgh · USUniversity of California, Davis · USAustralian Centre for Disease Preparedness · AUAustralian Research Council · AU

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI WHITE, JUDITH M. · 2003 to 2013
$91.5M
Immunology of Infectious DiseaseT32AI060525 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JoAnne L. Flynn · 2005 to 2026
$5.3M
Clostridium perfringens Type B-D Virulence PlasmidsR01AI056177 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MC CLANE, BRUCE A, ROOD, JULIAN · 2003 to 2013
$3.8M
Mechanisms of Action of C. Perfringens EnterotoxinR37AI019844 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MC CLANE, BRUCE A · 2005 to 2014
$3.0M
NIAID NIH HHS AI056177NIAID NIH HHS AI19488NIAID NIH HHS R01 AI056177NIAID NIH HHS R37 AI019844NIAID NIH HHS T32 AI060525NIAID NIH HHS U54 AI057168
6 · The paper itself

Abstract

Clostridium perfringens uses its arsenal of >16 toxins to cause histotoxic and intestinal infections in humans and animals. It has been unclear why this bacterium produces so many different toxins, especially since many target the plasma membrane of host cells. However, it is now established that C. perfringens uses chromosomally encoded alpha toxin (a phospholipase C) and perfringolysin O (a pore-forming toxin) during histotoxic infections. In contrast, this bacterium causes intestinal disease by employing toxins encoded by mobile genetic elements, including C. perfringens enterotoxin, necrotic enteritis toxin B-like, epsilon toxin and beta toxin. Like perfringolysin O, the toxins with established roles in intestinal disease form membrane pores. However, the intestinal disease-associated toxins vary in their target specificity, when they are produced (sporulation vs vegetative growth), and in their sensitivity to intestinal proteases. Producing many toxins with diverse characteristics likely imparts virulence flexibility to C. perfringens so it can cause an array of diseases.

Indexed as

Animal DiseasesAnimalsBacterial ToxinsClostridium InfectionsClostridium perfringensGas GangreneHumansIntestinesBacterial Toxins

Identifiers

PMID24762309
PMCPMC4155746
OpenAlexW2099792326

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.