Fishing for Targets of Alien Metabolites: A Novel Peroxisome Proliferator-Activated Receptor (PPAR) Agonist from a Marine Pest

Mar Drugs. 2018 Nov 3;16(11):431. doi: 10.3390/md16110431.

Abstract

Although the chemical warfare between invasive and native species has become a central problem in invasion biology, the molecular mechanisms by which bioactive metabolites from invasive pests influence local communities remain poorly characterized. This study demonstrates that the alkaloid caulerpin (CAU)-a bioactive component of the green alga Caulerpa cylindracea that has invaded the entire Mediterranean basin-is an agonist of peroxisome proliferator-activated receptors (PPARs). Our interdisciplinary study started with the in silico prediction of the ligand-protein interaction, which was then validated by in vivo, ex vivo and in vitro assays. On the basis of these results, we candidate CAU as a causal factor of the metabolic and behavioural disorders observed in Diplodus sargus, a native edible fish of high ecological and commercial relevance, feeding on C. cylindracea. Moreover, given the considerable interest in PPAR activators for the treatment of relevant human diseases, our findings are also discussed in terms of a possible nutraceutical/pharmacological valorisation of the invasive algal biomasses, supporting an innovative strategy for conserving biodiversity as an alternative to unrealistic campaigns for the eradication of invasive pests.

Keywords: Caulerpa cylindracea; Mediterranean; PPAR; biological invasions; caulerpin; molecular interactions.

Publication types

  • Video-Audio Media

MeSH terms

  • Animals
  • Biological Factors / metabolism
  • Biological Factors / pharmacology*
  • Caulerpa / metabolism*
  • Computer Simulation
  • Ecotoxicology
  • Fish Diseases / etiology*
  • Fish Diseases / metabolism
  • Food Chain
  • Indoles / metabolism
  • Indoles / toxicity*
  • Introduced Species*
  • Ligands
  • Models, Biological
  • Perciformes / physiology*
  • Peroxisome Proliferator-Activated Receptors / agonists*
  • Peroxisome Proliferator-Activated Receptors / metabolism

Substances

  • Biological Factors
  • Indoles
  • Ligands
  • Peroxisome Proliferator-Activated Receptors
  • caulerpin