Evidence map›Paper›PMID 28332578›Full record

ArticleScientific reports2017

A new class of inhibitors of the AraC family virulence regulator Vibrio cholerae ToxT.

Anne K Woodbrey, Evans O Onyango, Maria Pellegrini, Gabriela Kovacikova, Ronald K Taylor, Gordon W Gribble, F Jon Kull

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. mBio · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Fatty Acids AbolishMicrobiology spectrum · 2023
    Article
  8. Long Chain Fatty Acids and Virulence Repression in Intestinal Bacterial Pathogens.Frontiers in cellular and infection microbiology · 2022
    Review
  9. Article
  10. Review
  11. Combating Cholera.F1000Research · 2019
    Review
  12. Structural basis for virulence regulation inCommunications biology · 2019
    Article
  13. 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

7 authors at 1 institution in 1 country.

Anne K WoodbreyDepartment of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
Evans O OnyangoDepartment of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
Maria PellegriniDepartment of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
Gabriela KovacikovaDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, 03755, USA.
Ronald K TaylorDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, 03755, USA.
Gordon W GribbleDepartment of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
F Jon KullDepartment of Chemistry, Dartmouth College, Hanover, NH, 03755, USA.
Dartmouth College · US

Funding

Structural Analysis of Vibrio cholerae Virulence Gene Regulatory ProteinsR01AI072661 · NIAID · DARTMOUTH COLLEGE · PI KULL, FREDRICK JON · 2007 to 2016
$4.3M
Control of virulence in Vibrio cholerae by fatty acidsR01AI120068 · NIAID · DARTMOUTH COLLEGE · PI KULL, FREDRICK JON, SKORUPSKI, KAREN A · 2016 to 2020
$2.0M
Control of virulence in Vibrio cholerae by fatty acidsR56AI120068 · NIAID · DARTMOUTH COLLEGE · PI KULL, FREDRICK JON, SKORUPSKI, KAREN A · 2015 to 2015
$405k
NIAID NIH HHS R01 AI072661NIAID NIH HHS R01 AI120068NIAID NIH HHS R56 AI120068
6 · The paper itself

Abstract

Vibrio cholerae is responsible for the diarrheal disease cholera that infects millions of people worldwide. While vaccines protecting against cholera exist, and oral rehydration therapy is an effective treatment method, the disease will remain a global health threat until long-term solutions such as improved sanitation and access to clean water become widely available. Because of this, there is a pressing need for potent therapeutics that can either mitigate cholera symptoms, or act prophylactically to prevent the virulent effects of a cholera infection. Here we report the design, synthesis, and characterization of a set of compounds that bind and inhibit ToxT, the transcription factor that directly regulates the two primary V. cholerae virulence factors. Using the folded structure of the monounsaturated fatty acid observed in the X-ray structure of ToxT as a template, we designed ten novel compounds that inhibit the virulence cascade to a greater degree than any known inhibitor. Our findings provide a structural and functional basis for the development of viable antivirulence therapeutics that combat cholera and, potentially, other forms of bacterial pathogenic disease.

Indexed as

Vibrio choleraeAnti-Bacterial AgentsBacterial ProteinsBinding SitesCytarabineDNA-Binding ProteinsDrug DesignHumansMagnetic Resonance SpectroscopyModels, MolecularMolecular ConformationProtein BindingTranscription FactorsVirulence FactorsAnti-Bacterial AgentsBacterial ProteinsCytarabineDNA-Binding ProteinstcpN protein, Vibrio choleraeTranscription FactorsVirulence Factors

Identifiers

PMID28332578
PMCPMC5362913
OpenAlexW2599435127

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.