Evidence map›Paper›PMID 29432456›Full record

ArticlePLoS pathogens2018

GM1 ganglioside-independent intoxication by Cholera toxin.

Jakob Cervin, Amberlyn M Wands, Anna Casselbrant, Han Wu, Soumya Krishnamurthy, Aleksander Cvjetkovic, Johanna Estelius, Benjamin Dedic, Anirudh Sethi, Kerri-Lee Wallom and 9 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Cholera for travellers.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Review
  3. Gangliosides in molecular interactions and cell regulation.The Journal of biological chemistry · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. The diverse landscape of AB5-type toxins.Engineering microbiology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

19 authors at 4 institutions in 3 countries.

Jakob CervinDepartment of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-3840-1008
Amberlyn M WandsDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Anna CasselbrantDepartment of Gastrosurgical Research and Education, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Han WuDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, United States.ORCID 0000-0001-9791-0462
Soumya KrishnamurthyDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Aleksander CvjetkovicDepartment of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-9131-9791
Johanna EsteliusDepartment of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0003-0275-2559
Benjamin DedicDepartment of Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Anirudh SethiDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Kerri-Lee WallomDepartment of Pharmacology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-2842-1275
Rebecca RiiseSahlgrenska Cancer Center, University of Gothenburg, Gothenburg, Sweden.
Malin BäckströmMammalian Protein Expression Core Facility, University of Gothenburg, Gothenburg, Sweden.
Ville WalleniusDepartment of Gastrosurgical Research and Education, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Frances M PlattDepartment of Pharmacology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-7614-0403
Michael LebensDepartment of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0001-9458-9474
Susann TenebergDepartment of Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Lars FändriksDepartment of Gastrosurgical Research and Education, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Jennifer J KohlerDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, United States.ORCID 0000-0001-5373-3329
Ulf YrlidDepartment of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-3431-6770
University of Gothenburg · SEThe University of Texas Southwestern Medical Center · USUniversity of Oxford · GBSahlgrenska University Hospital · SE

Funding

Study of sialoside function using photocrosslinking sialic acidR01GM090271 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI KOHLER, JENNIFER J · 2009 to 2021
$4.4M
Medical Research Council G0700969NIGMS NIH HHS R01 GM090271Wellcome Trust
6 · The paper itself

Abstract

Cholera toxin (CT) enters and intoxicates host cells after binding cell surface receptors via its B subunit (CTB). We have recently shown that in addition to the previously described binding partner ganglioside GM1, CTB binds to fucosylated proteins. Using flow cytometric analysis of primary human jejunal epithelial cells and granulocytes, we now show that CTB binding correlates with expression of the fucosylated Lewis X (LeX) glycan. This binding is competitively blocked by fucosylated oligosaccharides and fucose-binding lectins. CTB binds the LeX glycan in vitro when this moiety is linked to proteins but not to ceramides, and this binding can be blocked by mAb to LeX. Inhibition of glycosphingolipid synthesis or sialylation in GM1-deficient C6 rat glioma cells results in sensitization to CT-mediated intoxication. Finally, CT gavage produces an intact diarrheal response in knockout mice lacking GM1 even after additional reduction of glycosphingolipids. Hence our results show that CT can induce toxicity in the absence of GM1 and support a role for host glycoproteins in CT intoxication. These findings open up new avenues for therapies to block CT action and for design of detoxified enterotoxin-based adjuvants.

Indexed as

AnimalsCells, CulturedCholera ToxinGlycosylationG(M1) GangliosideHL-60 CellsHumansJurkat CellsMiceMice, Inbred C57BLMice, KnockoutN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferaseRatsCholera ToxinG(M1) GangliosideN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferase

Identifiers

PMID29432456
PMCPMC5825173
OpenAlexW2787740035

What OpenQuestion holds

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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.