期刊
MARINE DRUGS
卷 11, 期 10, 页码 3718-3734出版社
MDPI AG
DOI: 10.3390/md11103718
关键词
diarrhetic shellfish poisoning (DSP); diarrhetic shellfish toxins (DSTs); okadaic acid; rapid screening test; LC-MS; MS; protein phosphatase 2A (PP2A); enzyme-linked immunosorbent assay (ELISA); Jellett rapid test; Puget Sound
资金
- United States Environmental Protection Agency (EPA) through their National Estuary Program [PC-00J32601]
- NOAA's National Center for Coastal Ocean Sciences' Event Response program (NOAA ER)
The illness of three people due to diarrhetic shellfish poisoning (DSP) following their ingestion of recreationally harvested mussels from Sequim Bay State Park in the summer of 2011, resulted in intensified monitoring for diarrhetic shellfish toxins (DSTs) in Washington State. Rapid testing at remote sites was proposed as a means to provide early warning of DST events in order to protect human health and allow growers to test pre-harvest shellfish samples, thereby preventing harvest of toxic product that would later be destroyed or recalled. Tissue homogenates from several shellfish species collected from two sites in Sequim Bay, WA in the summer 2012, as well as other sites throughout Puget Sound, were analyzed using three rapid screening methods: a lateral flow antibody-based test strip (Jellett Rapid Test), an enzyme-linked immunosorbent assay (ELISA) and a protein phosphatase 2A inhibition assay (PP2A). The results were compared to the standard regulatory method of liquid chromatography coupled with tandem mass spectroscopy (LC-MS/MS). The Jellett Rapid Test for DSP gave an unacceptable number of false negatives due to incomplete extraction of DSTs using the manufacturer's recommended method while the ELISA antibody had low cross-reactivity with dinophysistoxin-1, the major toxin isomer in shellfish from the region. The PP2A test showed the greatest promise as a screening tool for Washington State shellfish harvesters.
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