Effects of a skin neuropeptide (substance p) on cutaneous microflora

PLoS One. 2013 Nov 8;8(11):e78773. doi: 10.1371/journal.pone.0078773. eCollection 2013.

Abstract

Background: Skin is the largest human neuroendocrine organ and hosts the second most numerous microbial population but the interaction of skin neuropeptides with the microflora has never been investigated. We studied the effect of Substance P (SP), a peptide released by nerve endings in the skin on bacterial virulence.

Methodology/principal findings: Bacillus cereus, a member of the skin transient microflora, was used as a model. Exposure to SP strongly stimulated the cytotoxicity of B. cereus (+553±3% with SP 10(-6) M) and this effect was rapid (<5 min). Infection of keratinocytes with SP treated B. cereus led to a rise in caspase1 and morphological alterations of the actin cytoskeleton. Secretome analysis revealed that SP stimulated the release of collagenase and superoxide dismutase. Moreover, we also noted a shift in the surface polarity of the bacteria linked to a peel-off of the S-layer and the release of S-layer proteins. Meanwhile, the biofilm formation activity of B. cereus was increased. The Thermo unstable ribosomal Elongation factor (Ef-Tu) was identified as the SP binding site in B. cereus. Other Gram positive skin bacteria, namely Staphylococcus aureus and Staphylococcus epidermidis also reacted to SP by an increase of virulence. Thermal water from Uriage-les-Bains and an artificial polysaccharide (Teflose®) were capable to antagonize the effect of SP on bacterial virulence.

Conclusions/significance: SP is released in sweat during stress and is known to be involved in the pathogenesis of numerous skin diseases through neurogenic inflammation. Our study suggests that a direct effect of SP on the skin microbiote should be another mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus cereus / growth & development
  • Bacillus cereus / metabolism*
  • Biofilms / growth & development
  • Calcitonin Gene-Related Peptide
  • Humans
  • Keratinocytes / metabolism
  • Neurosecretory Systems / metabolism
  • Skin / metabolism*
  • Staphylococcus aureus / metabolism*
  • Staphylococcus aureus / pathogenicity
  • Substance P / metabolism*
  • Virulence / genetics

Substances

  • Substance P
  • Calcitonin Gene-Related Peptide

Grants and funding

This work was supported by the FUI program Skin-O-Flor certified by the world’s leading perfumery cosmetics network Cosmetic Valley and financed by the French Government (DGCIS), European Union (FEDER), Department of Eure et Loir and the Regions Centre and Haute-Normandie. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.