Biomarkers of brevetoxin exposure and composite toxin levels in hard clam (Mercenaria sp.) exposed to Karenia brevis blooms

Toxicon. 2015 Mar:96:82-8. doi: 10.1016/j.toxicon.2015.01.014. Epub 2015 Jan 22.

Abstract

Brevetoxins in clams (Mercenaria sp.) exposed to recurring blooms of Karenia brevis in Sarasota Bay, FL, were studied over a three-year period. Brevetoxin profiles in toxic clams were generated by ELISA and LC-MS. Several brevetoxin metabolites, as identified by LC-MS, were major contributors to the composite brevetoxin response of ELISA. These were S-desoxyBTX-B2 (m/z 1018), BTX-B2 (m/z 1034), BTX-B5 (m/z 911), open A-ring BTX-B5 (m/z 929), and BTX-B1 (m/z 1018). Summed values of these metabolites were highly correlated (R(2) = 0.9) with composite B-type brevetoxin measurements by ELISA. S-desoxyBTX-B2, BTX-B2, and BTX-B1 were the most persistent and detectable in shellfish for several months after dissipation of blooms. These metabolites were selected as LC-MS biomarkers of brevetoxin exposure and reflective of composite B-type brevetoxins in hard clam. ELISA and LC-MS values were moderately correlated with toxicity of the shellfish by mouse bioassay. ELISA and LC-MS methods offer rapid screening and confirmatory determination of brevetoxins, respectively, as well as toxicity assessment in clams exposed to K. brevis blooms.

Keywords: Biomarkers; Brevetoxins; Hard clams; Karenia brevis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Assay
  • Biomarkers / metabolism*
  • Bivalvia / drug effects
  • Bivalvia / metabolism*
  • Chromatography, Liquid
  • Dinoflagellida / chemistry*
  • Environmental Exposure*
  • Enzyme-Linked Immunosorbent Assay
  • Florida
  • Harmful Algal Bloom*
  • Marine Toxins / analysis
  • Marine Toxins / toxicity*
  • Mass Spectrometry
  • Mice
  • Molecular Structure
  • Oxocins / analysis
  • Oxocins / toxicity*
  • Time Factors

Substances

  • Biomarkers
  • Marine Toxins
  • Oxocins
  • brevetoxin