Toxic responses of metabolites produced by Ostreopsis cf. ovata on a panel of cell types

Rachelle Lanceleur1, Marin-Pierre Gémin2, Anne-Louise Blier1

  • 1ANSES, Fougères Laboratory, Toxicology of Contaminants Unit, French Agency for Food, Environmental and Occupational Health & Safety, Fougères, 35 306, France.

Insights

Blooms of Ostreopsis cf. ovata produce ovatoxins (OVTXs), causing human intoxications. This study investigated OVTX toxicity across various cell types, revealing cytotoxic and pro-inflammatory effects, though distinct from palytoxin mechanisms.

Area of Science:

  • Marine Biology
  • Toxicology
  • Cell Biology

Background:

  • Blooms of Ostreopsis cf. ovata are linked to human intoxications.
  • Ovatoxins (OVTXs) are the primary toxins, analogous to palytoxin (PlTX).
  • Limited toxicity data exists for OVTXs due to a lack of commercial standards.

Purpose of the Study:

  • To assess the toxicity of OVTXs on various human cell types.
  • To compare the effects of OVTXs with palytoxin (PlTX).
  • To investigate the mechanisms behind OVTX-induced cytotoxicity and inflammation.

Main Methods:

  • Generated extracts and purified OVTX-a and OVTX-d from Mediterranean O. cf. ovata strains.
  • Tested chemical samples and PlTX on cell lines from skin, intestine, lung, liver, and nervous system.
  • Assessed cytotoxicity and interleukin-8 (IL-8) release as indicators of inflammatory response.

Main Results:

  • O. cf. ovata extracts showed dose-dependent cytotoxicity and increased IL-8 release in keratinocytes.
  • OVTX-containing fractions were cytotoxic, with IL-8 induction primarily in liver cells.
  • Non-OVTX fractions also exhibited cytotoxicity and pro-inflammatory effects in lung and liver cells.
  • OVTX-a and OVTX-d displayed similar cytotoxicity, with minor differences in intestinal and skin cells.
  • Only PlTX induced significant pro-inflammatory effects, mainly in keratinocytes.

Conclusions:

  • OVTXs are cytotoxic to multiple cell types, sharing the Na+/K+ ATPase target with PlTX.
  • Distinct mechanisms likely explain the differing pro-inflammatory effects between OVTXs and PlTX.
  • Further research is needed to elucidate the non-OVTX components' roles in toxicity and inflammation.

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