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12th International Conference on Harmful Algae

12th International Conference on Harmful Algae

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INTERNATIONAL SOCIETY FOR THE STUDY OF HARMFUL ALGAE12 th <str<strong>on</strong>g>Internati<strong>on</strong>al</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Harmful</strong> <strong>Algae</strong>, Copenhagen, Denmark, 4-8 September 2006POSTER ABSTRACTSPO.05-35Liquid chromatography-tandemmass spectrometry techniquesfor the discovery of new marinealgal toxin analogues andmetabolitesSessi<strong>on</strong>: PO.05 - Toxin analysisJAB Aasen 1 , MA Quilliam 21 Norwegian School of Veterinary Science,OSLO, Norway2 Institute for Marine Biosciences, NRC,HALIFAX, NOVA SCOTIA, CanadaIn recent years the number ofknown marine algal toxins hasincreased tremendously, mainly bydiscovery of new analogues andmetabolites within known toxingroups. This is due in particular tothe use of LC-MS/MS. In thispresentati<strong>on</strong>, we will outline somenew strategies based <strong>on</strong> variousMS/MS scanning techniques thatcan be used for comprehensivedetecti<strong>on</strong> and identificati<strong>on</strong> of newstructural analogues of toxins. Oneexample is the detecti<strong>on</strong> of assortednew analogues of the cyclic iminetoxins, spirolides (SPX). Targetingkey collisi<strong>on</strong>-induced product i<strong>on</strong>s(m/z 150 or 164) in a precursor i<strong>on</strong>scanning mode and presenting thei<strong>on</strong> intensity data in a 2-D c<strong>on</strong>tourplot (m/z vs. retenti<strong>on</strong> time) allowedthe detecti<strong>on</strong> of new toxins asindividual 'spots' and alsodetermines their masses. Producti<strong>on</strong> scans of those masses thenallow detailed structure informati<strong>on</strong>to be generated. Thus, several newSPX analogues including fatty acidacyl ester metabolites have beenidentified. Examples will also beshown for the yessotoxin (YTX),okadaic acid (OA) and pectenotoxin(PTX) groups. The discovery of allthese new toxin analogues raisessome important questi<strong>on</strong>s such astheir toxicological significance andwhether we will be able to m<strong>on</strong>itorfor the toxins without standards.PO.04-12Statewide distributi<strong>on</strong> ofsaxitoxins within Florida pufferfish speciesSessi<strong>on</strong>: PO.04 – Food chainsJP Abbott, JH Landsberg, LJFlewelling, L Sebastian, S StahlFlorida Fish and Wildlife C<strong>on</strong>servati<strong>on</strong> C,ST. PETERSBURG, United States ofAmericaFrom January 2002 to April 2005,28 cases of puffer fish pois<strong>on</strong>ing(PFP) were reported, primarily fromFlorida. A harvesting ban was putinto effect in April 2002. Previouslyunknown in Florida’s marine waters,all incidents were due to saxitoxinpresent in the muscle of southernpuffer fish (Sphoeroides nephelus)originating from the northern IndianRiver Lago<strong>on</strong> (IRL) <strong>on</strong> Florida’sAtlantic coast. Southern puffer fishin the IRL c<strong>on</strong>tinue to pose asignificant threat to public healthwith maximum levels in the musclejust over 20,106 µg STXeq./100 gtissue (n=384), (acti<strong>on</strong> level forshellfish is 80 µg STXeq./100gtissue). Lower levels, ranging from10 to 3133 µg STXeq./100g tissue,have also been found in the muscleof southern puffer fish fromApalachicola (northwest),Jacks<strong>on</strong>ville (northeast), FloridaKeys (south), Charlotte Harbor(southwest), Tampa Bay (centralwest) and Tequesta (southeast).Checkered (S. testudineus) pufferfish from the Florida Keys, IRL andTequesta (range= 17 to 137 µgSTXeq./100g tissue) were generallymuch lower than southern puffers.118

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