Evidence map›Paper›PMID 27991578›Full record

ArticleScientific reports2016

Ribavirin suppresses bacterial virulence by targeting LysR-type transcriptional regulators.

Rahul Shubhra Mandal, Atri Ta, Ritam Sinha, Nagaraja Theeya, Anirban Ghosh, Mohsina Tasneem, Anirban Bhunia, Hemanta Koley, Santasabuj Das

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  5. Fabrication and evaluation of ribavirin-loaded electrospun nanofibers as an antimicrobial wound dressing.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
  6. Structural Insights into Regulation of Vibrio Virulence Gene Networks.Advances in experimental medicine and biology · 2023
    Article
  7. Article
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  10. Article
  11. Review
  12. Article
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  14. Article
  15. A high-throughput system to identify inhibitors ofProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Review
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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

9 authors at 2 institutions in 1 country.

Rahul Shubhra MandalBiomedical Informatics Center, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Atri TaDivision of Clinical Medicine, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Ritam SinhaDivision of Bacteriology, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Nagaraja TheeyaDivision of Clinical Medicine, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Anirban GhoshDepartment of Biophysics, Bose Institute, Kolkata, India.
Mohsina TasneemBiomedical Informatics Center, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Anirban BhuniaDepartment of Biophysics, Bose Institute, Kolkata, India.
Hemanta KoleyDivision of Bacteriology, National Institute of Cholera and Enteric Diseases, Kolkata, India.
Santasabuj DasBiomedical Informatics Center, National Institute of Cholera and Enteric Diseases, Kolkata, India.
National Institute of Cholera and Enteric Diseases · INBose Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting bacterial virulence mechanisms without compromising bacterial growth is a promising strategy to prevent drug resistance. LysR-type transcriptional regulators (LTTRs) possess structural conservation across bacterial species and regulate virulence in numerous pathogens, making them attractive targets for antimicrobial agents. We targeted AphB, a Vibrio cholerae LTTR, which regulates the expression of genes encoding cholera toxin and toxin-co-regulated pilus for inhibitor designing. Since AphB ligand is unknown, we followed a molecular fragment-based approach for ligand designing using FDA-approved drugs and subsequent screen to identify molecules that exhibited high-affinity binding to AphB ligand-binding pocket. Among the identified compounds, ribavirin, an anti-viral drug, antagonized AphB functions. Ribavirin perturbed Vibrio cholerae pathogenesis in animal models. The inhibitory effects of the drug was limited to the bacteria expressing wild type AphB, but not its constitutively active mutant (AphB

Indexed as

Gene Expression Regulation, BacterialAnimalsBacterial ProteinsDrug RepositioningLigandsMaleMiceMolecular ConformationMutationPromoter Regions, GeneticProtein BindingRabbitsRibavirinSalmonella typhiSubstrate SpecificityTrans-ActivatorsAphB protein, Vibrio choleraeBacterial ProteinsLigandsLysR protein, BacteriaRibavirinTrans-ActivatorsTranscription Factors

Identifiers

PMID27991578
PMCPMC5171790
OpenAlexW2564553224

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.