Evidence map›Paper›PMID 25093328›Full record

ArticlePloS one2014

The periplasmic protein TolB as a potential drug target in Pseudomonas aeruginosa.

Alessandra Lo Sciuto, Regina Fernández-Piñar, Lucia Bertuccini, Francesca Iosi, Fabiana Superti, Francesco Imperi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 63 citations in OpenAlex.

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  8. Targeting Iron - Respiratory Reciprocity Promotes Bacterial Death.bioRxiv : the preprint server for biology · 2024
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  12. Chlorogenic Acid InhibitsMicroorganisms · 2023
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  13. Article
  14. Review
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  17. Article
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  19. Endogenous membrane stress induces T6SS activity inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

6 authors at 1 institution in 1 country.

Alessandra Lo SciutoDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.
Regina Fernández-PiñarDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy.
Lucia BertucciniUltrastructural Infectious Pathology Section, Department of Technology and Health, National Institute of Health, Rome, Italy.
Francesca IosiUltrastructural Infectious Pathology Section, Department of Technology and Health, National Institute of Health, Rome, Italy.
Fabiana SupertiUltrastructural Infectious Pathology Section, Department of Technology and Health, National Institute of Health, Rome, Italy.
Francesco ImperiDepartment of Biology and Biotechnology "Charles Darwin", Sapienza University of Rome, Rome, Italy; Pasteur Institute-Cenci Bolognetti Foundation, Sapienza University of Rome, Rome, Italy.
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Gram-negative bacterium Pseudomonas aeruginosa is one of the most dreaded pathogens in the hospital setting, and represents a prototype of multi-drug resistant "superbug" for which effective therapeutic options are very limited. The identification and characterization of new cellular functions that are essential for P. aeruginosa viability and/or virulence could drive the development of anti-Pseudomonas compounds with novel mechanisms of action. In this study we investigated whether TolB, the periplasmic component of the Tol-Pal trans-envelope protein complex of Gram-negative bacteria, represents a potential drug target in P. aeruginosa. By combining conditional mutagenesis with the analysis of specific pathogenicity-related phenotypes, we demonstrated that TolB is essential for P. aeruginosa growth, both in laboratory and clinical strains, and that TolB-depleted P. aeruginosa cells are strongly defective in cell-envelope integrity, resistance to human serum and several antibiotics, as well as in the ability to cause infection and persist in an insect model of P. aeruginosa infection. The essentiality of TolB for P. aeruginosa growth, resistance and pathogenicity highlights the potential of TolB as a novel molecular target for anti-P. aeruginosa drug discovery.

Indexed as

Drug DiscoveryMolecular Targeted TherapyAnti-Bacterial AgentsDrug Resistance, BacterialHumansMicrobial Sensitivity TestsOrganisms, Genetically ModifiedPeriplasmic ProteinsPolymyxinsPseudomonas aeruginosaPseudomonas InfectionsAnti-Bacterial AgentsPeriplasmic ProteinsPolymyxins

Identifiers

PMID25093328
PMCPMC4122361
OpenAlexW2001470060

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.