Evidence map›Paper›PMID 28209403›Full record

ReviewTrends in pharmacological sciences2017

Small Molecules That Sabotage Bacterial Virulence.

Benjamin K Johnson, Robert B Abramovitch

Abstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
–field-weighted citation impact
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

67 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Orally available designed miniproteins inhibit enterotoxigenicbioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. AACS synthetic biology · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Evaluation of Expanded 2-Aminobenzothiazole Library for Inhibition ofbioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

7 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

2 authors.

Benjamin K JohnsonDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
Robert B AbramovitchDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA. Electronic address: abramov5@msu.edu.

Funding

Mechanisms of Mycobacterium Tuberculosis pH-driven AdaptationR01AI116605 · NIAID · MICHIGAN STATE UNIVERSITY · PI ABRAMOVITCH, ROBERT B · 2016 to 2020
$1.9M
Non-competitive proteasome inhibitors to treat chronic, drug-resistant tuberculosisR21AI117018 · NIAID · MICHIGAN STATE UNIVERSITY · PI ABRAMOVITCH, ROBERT B, TEPE, JETZE J. · 2016 to 2017
$400k
Screening for inhibitors of M. tuberculosis persistence-related lipid metabolismR21AI105867 · NIAID · MICHIGAN STATE UNIVERSITY · PI ABRAMOVITCH, ROBERT B · 2013 to 2014
$392k
NIAID NIH HHS R01 AI116605NIAID NIH HHS R21 AI105867NIAID NIH HHS R21 AI117018
6 · The paper itself

Abstract

The continued rise of antibiotic-resistant bacterial infections has motivated alternative strategies for target discovery and treatment of infections. Antivirulence therapies function through inhibition of in vivo required virulence factors to disarm the pathogen instead of directly targeting viability or growth. This approach to treating bacteria-mediated diseases may have advantages over traditional antibiotics because it targets factors specific for pathogenesis, potentially reducing selection for resistance and limiting collateral damage to the resident microbiota. This review examines vulnerable molecular mechanisms used by bacteria to cause disease and the antivirulence compounds that sabotage these virulence pathways. By expanding the study of antimicrobial targets beyond those that are essential for growth, antivirulence strategies offer new and innovative opportunities to combat infectious diseases.

Indexed as

Anti-Bacterial AgentsArtemisininsBacteriaBacterial AdhesionBacterial ProteinsEthoxzolamideFimbriae, BacterialHistidine KinaseSulfonamidesVirulenceAnti-Bacterial AgentsartemisininArtemisininsBacterial ProteinsCrl protein, BacteriaEthoxzolamideHistidine KinaseLED209Sulfonamidesantivirulence therapiesbacterial pathogenesis

Identifiers

PMID28209403
PMCPMC5679398

What OpenQuestion holds

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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.