Transcriptional and biochemical analysis of antioxidant enzymes in the mussel Mytilus galloprovincialis during experimental exposures to the toxic dinoflagellate Prorocentrum lima

Mar Environ Res. 2017 Aug:129:304-315. doi: 10.1016/j.marenvres.2017.06.009. Epub 2017 Jun 15.

Abstract

The genotoxic and cytotoxic effects of Diarrhetic Shellfish Poisoning (DSP) toxins have been widely investigated in bivalve molluscs, representing the main vectors of these compounds in the Atlantic coast of Europe. DSP toxins are produced by Harmful Algal Blooms (HABs) of Dinophysis and Prorocentrum dinoflagellates, being subsequently accumulated by marine organisms and biomagnified throughout trophic webs. Yet, bivalves display increased resistance to the harmful effects of these toxins during HAB episodes. While previous reports have suggested that such resilience might be the result of an increased activity in the bivalve antioxidant system, very little is still known about the specific mechanism underlying the protective effect observed in these organisms. The present work aims to fill this gap by studying transcriptional expression levels and biochemical activities of antioxidant enzymes in different tissues the mussel Mytilus galloprovincialis during experimental exposures to DSP toxins produced by the dinoflagellate Prorocentrum lima. Results are consistent with the presence of a compensatory mechanism involving a down-regulation in the expression of specific genes encoding antioxidant enzymes [i.e., SuperOxide Dismutase (SOD) and CATalase (CAT)] which is counterbalanced by the up-regulation of other antioxidant genes such as Glutathione S-Transferase pi-1 (GST-pi) and Selenium-dependent Glutathione PeroXidase (Se-GPx), respectively. Enzymatic activity analyses mirror gene expression results, revealing high antioxidant activity levels (consistent with a protective role for the antioxidant system) along with reduced lipid peroxidation (increasing the defense against oxidative stress).

Keywords: Antioxidant enzymes; Bivalves; Diarrhetic shellfish toxins; Gene expression; Lipid peroxidation; Oxidative stress.

MeSH terms

  • Animals
  • Catalase / metabolism
  • Dinoflagellida / physiology*
  • Environmental Monitoring
  • Europe
  • Glutathione Peroxidase / metabolism
  • Harmful Algal Bloom*
  • Marine Toxins / toxicity*
  • Mytilus / physiology*
  • Superoxide Dismutase / metabolism

Substances

  • Marine Toxins
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase