A cytotoxicity assay for the detection and differentiation of two families of shellfish toxins

A. F. Flanagan, K. R. Callanan, J. Donlon, R. Palmer, A. Forde, M. Kane

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

60 Citations (Scopus)

Abstract

There is an urgent need for an alternative to the mouse bioassay for the detection of algal toxins in shellfish on both analytical and animal welfare grounds. Several alternative methodologies have been described, but have not gained widespread acceptance to date, because each assay measures only one or a small number of related phycotoxins out of the increasing range that needs to be detected. A simple cytotoxicity assay using either the HepG2 or ECV-304 cell lines is described with two end-point measurements, which can detect and distinguish between two unrelated classes of phycotoxins. Morphological examination following 3 h exposure to the sample enables the detection of the diarrhetic shellfish poisons, including okadaic acid and related toxins. Viability testing using MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide), following 24 h exposure of the same cells to the sample, reveals a second class of toxin, which is most probably the newly-described toxin, azaspiracid. This assay should play an important role in shellfish monitoring in the future.

Original languageEnglish
Pages (from-to)1021-1027
Number of pages7
JournalToxicon
Volume39
Issue number7
DOIs
Publication statusPublished - 1 Jul 2001

Keywords

  • AZP
  • Azaspiracid
  • Cytotoxicity assay
  • DSP
  • Infremer mouse bioassay
  • Phycotoxin

Fingerprint

Dive into the research topics of 'A cytotoxicity assay for the detection and differentiation of two families of shellfish toxins'. Together they form a unique fingerprint.

Cite this