Evidence map›Paper›PMID 25938431›Full record

ArticlePloS one2015

Violacein Treatment Modulates Acute and Chronic Inflammation through the Suppression of Cytokine Production and Induction of Regulatory T Cells.

Liana Verinaud, Stefanie Costa Pinto Lopes, Isabel Cristina Naranjo Prado, Fábio Zanucoli, Thiago Alves da Costa, Rosária Di Gangi, Luidy Kazuo Issayama, Ana Carolina Carvalho, Amanda Pires Bonfanti, Guilherme Francio Niederauer and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
2.0field-weighted citation impact, top 17% 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, 38 citations in OpenAlex.

  1. Violacein-Loaded Outer Membrane Vesicles fromACS biomaterials science & engineering · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Multi-target drug with potential applications: violacein in the spotlight.World journal of microbiology & biotechnology · 2021
    Review
  9. Microbiota, renal disease and renal transplantation.World journal of transplantation · 2021
    Review
  10. Review
  11. Article
  12. 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

16 authors at 1 institution in 1 country.

Liana VerinaudDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Stefanie Costa Pinto LopesDepartment of Genetics Evolution and Bioagents, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Isabel Cristina Naranjo PradoDepartment of Genetics Evolution and Bioagents, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Fábio ZanucoliDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Thiago Alves da CostaDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Rosária Di GangiDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Luidy Kazuo IssayamaDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Ana Carolina CarvalhoDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Amanda Pires BonfantiDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Guilherme Francio NiederauerDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Nelson DuranBiological Chemistry Laboratory, Chemistry Institute, University of Campinas, Campinas, SP, Brazil; Laboratory of Nanostructured Synthesis and Biosystems Interactions (NanoBioss), Chemistry Institute, University of Campinas, Campinas, SP, Brazil.
Fábio Trindade Maranhão CostaDepartment of Genetics Evolution and Bioagents, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Alexandre Leite Rodrigues OliveiraDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Maria Alice da Cruz HöflingDepartment of Histology and Embryology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Dagmar Ruth Stach MachadoDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Rodolfo ThoméDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is a necessary process to control infection. However, exacerbated inflammation, acute or chronic, promotes deleterious effects in the organism. Violacein (viola), a quorum sensing metabolite from the Gram-negative bacterium Chromobacterium violaceum, has been shown to protect mice from malaria and to have beneficial effects on tumors. However, it is not known whether this drug possesses anti-inflammatory activity. In this study, we investigated whether viola administration is able to reduce acute and chronic autoimmune inflammation. For that purpose, C57BL/6 mice were intraperitoneally injected with 1 μg of LPS and were treated with viola (3.5mg/kg) via i.p. at the same time-point. Three hours later, the levels of inflammatory cytokines in the sera and phenotypical characterization of leukocytes were determined. Mice treated with viola presented a significant reduction in the production of inflammatory cytokines compared with untreated mice. Interestingly, although viola is a compound derived from bacteria, it did not induce inflammation upon administration to naïve mice. To test whether viola would protect mice from an autoimmune inflammation, Experimental Autoimmune Encephalomyelitis (EAE)-inflicted mice were given viola i.p. at disease onset, at the 10th day from immunization. Viola-treated mice developed mild EAE disease in contrast with placebo-treated mice. The frequencies of dendritic cells and macrophages were unaltered in EAE mice treated with viola. However, the sole administration of viola augmented the levels of splenic regulatory T cells (CD4+Foxp3+). We also found that adoptive transfer of viola-elicited regulatory T cells significantly reduced EAE. Our study shows, for the first time, that violacein is able to modulate acute and chronic inflammation. Amelioration relied in suppression of cytokine production (in acute inflammation) and stimulation of regulatory T cells (in chronic inflammation). New studies must be conducted in order to assess the possible use of viola in therapeutic approaches in human autoimmune diseases.

Indexed as

Adoptive TransferAnimalsAnti-Inflammatory AgentsBiomarkersCytokinesDendritic CellsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleIndolesInflammationInflammation MediatorsLipopolysaccharidesLymphocyte CountMiceSeverity of Illness IndexAnti-Inflammatory AgentsBiomarkersCytokinesIndolesInflammation MediatorsLipopolysaccharidesviolacein

Identifiers

PMID25938431
PMCPMC4418714
OpenAlexW746699443

What OpenQuestion holds

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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.