Evidence map›Paper›PMID 21930894›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Lipolysis-stimulated lipoprotein receptor (LSR) is the host receptor for the binary toxin Clostridium difficile transferase (CDT).

Panagiotis Papatheodorou, Jan E Carette, George W Bell, Carsten Schwan, Gregor Guttenberg, Thijn R Brummelkamp, Klaus Aktories

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

113 citing papers in PubMed, 188 citations in OpenAlex.

  1. Review
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  9. Article
  10. Review
  11. Clinical microbiology reviews · 2024
    Review
  12. Review
  13. Trauma-toxicology: concepts, causes, complications.Naunyn-Schmiedeberg's archives of pharmacology · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Immunization Strategies Against Clostridioides difficile.Advances in experimental medicine and biology · 2024
    Review
  18. Review
  19. Review
  20. Review

53 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

7 authors at 2 institutions in 2 countries.

Panagiotis PapatheodorouInstitut für Experimentelle und Klinische Pharmakologie und Toxikologie, Albert-Ludwigs-Universität Freiburg, D-79104 Freiburg, Germany.
Jan E Carette
George W Bell
Carsten Schwan
Gregor Guttenberg
Thijn R Brummelkamp
Klaus Aktories
University of Freiburg · DEWhitehead Institute for Biomedical Research · US

Funding

A new system for mammalian cell genetics using a haploid genomic contextR21HG004938 · NHGRI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI BRUMMELKAMP, THIJN · 2009 to 2010
$536k
NHGRI NIH HHS R21 HG004938NHGRI NIH HHS R21-HG004938-01
6 · The paper itself

Abstract

Clostridium difficile infection (CDI) causes antibiotic-associated diarrhea and pseudomembranous colitis. Hypervirulent strains of the pathogen, which are responsible for increased morbidity and mortality of CDI, produce the binary actin-ADP ribosylating toxin Clostridium difficile transferase (CDT) in addition to the Rho-glucosylating toxins A and B. CDT depolymerizes the actin cytoskeleton, increases adherence and colonization of Clostridia by induction of microtubule-based cell protrusions and, eventually, causes death of target cells. Using a haploid genetic screen, we identified the lipolysis-stimulated lipoprotein receptor as the membrane receptor for CDT uptake by target cells. Moreover, we show that Clostridium perfringens iota toxin, which is a related binary actin-ADP ribosylating toxin, enters target cells via the lipolysis-stimulated lipoprotein receptor. Identification of the toxin receptors is essential for understanding of the toxin uptake and provides a most valuable basis for antitoxin strategies.

Indexed as

Clostridioides difficileEnterotoxinsHaploidyHeLa CellsHumansReceptors, LDLTransferasesenterotoxin, ClostridiumEnterotoxinslipolysis-stimulated receptorReceptors, LDLTransferases

Identifiers

PMID21930894
PMCPMC3182710
OpenAlexW1964262120

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.