PLoS ONE (Jan 2015)

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,
  • Nelson Duran,
  • Fábio Trindade Maranhão Costa,
  • Alexandre Leite Rodrigues Oliveira,
  • Maria Alice da Cruz Höfling,
  • Dagmar Ruth Stach Machado,
  • Rodolfo Thomé

DOI
https://doi.org/10.1371/journal.pone.0125409
Journal volume & issue
Vol. 10, no. 5
p. e0125409

Abstract

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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.