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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 2006cell size depended <strong>on</strong> the strainused and not <strong>on</strong> the salinity of thegrowth medium.PO.15-06PCR-based m<strong>on</strong>itoring of toxicdinoflagellates in aMediterranean shellfish farmSessi<strong>on</strong>: PO.15 - M<strong>on</strong>itoringElena Bertozzini 1 , Luca Galluzzi 2 ,Ant<strong>on</strong>ella Penna 1 , Maria Giacobbe 3 ,Federico Perini 2 , AlessandraPigalarga 2 , Silvia Prioli 4 , MauroMagnani 21 Università degli Studi di Urbino, PESARO,Italy2 University of Urbino, FANO, Italy3 IAMC, CNR, MESSINA, Italy4 Coop. MARE, CATTOLICA, ItalyParalytic Shellfish Pois<strong>on</strong>ing (PSP)and Diarrhetic Shellfish Pois<strong>on</strong>ing(DSP) are syndromes caused byc<strong>on</strong>sumpti<strong>on</strong> of shellfishc<strong>on</strong>taminated with toxins producedby several species of marinedinoflagellates. The standardm<strong>on</strong>itoring of shellfish farms for thepresence of harmful algae andrelated toxins usually requiresmicroscopic examinati<strong>on</strong> ofphytoplankt<strong>on</strong>, bioassays and toxindeterminati<strong>on</strong> by HPLC. Molecularbiology techniques may be helpfulin the detecti<strong>on</strong> of target microalgaein c<strong>on</strong>taminated mussels.A qualitative PCR assay for therapid detecti<strong>on</strong> of the generaAlexandrium and Dinophysis inseawater samples and musseltissues was developed. Thismethod was tested in a m<strong>on</strong>itoringprogram in a shellfish farm al<strong>on</strong>gthe NW Adriatic Sea and I<strong>on</strong>iancoast of Italy during 13 m<strong>on</strong>ths. Inseawater samples, the PCR methodhas generally shown a greatersensitivity compared to microscopeanalysis. Instead, the detecti<strong>on</strong> ofgenera Alexandrium and Dinophysisin mussel tissues poorly reflectedthe presence of thesedinoflagellates in the corresp<strong>on</strong>dingseawater samples. However, noDSP toxicity was found in musselsduring the entire m<strong>on</strong>itoringprogram. Even if no correlati<strong>on</strong> wasfound between the presence ofalgal DNA and toxin accumulati<strong>on</strong> inmussels, the detecti<strong>on</strong> of harmfulalgae DNA could furnish an earlywarning for potential mussel toxicityPO.02-06Molecular physiology of thetoxigenic haptophytePrymnesium parvumSessi<strong>on</strong>: PO.02 - GenomicsS Beszteri 1 , U Tillmann 1 , M Freitag 1 , GGlöckner 2 , AD Cembella 1 , U John 11 Alfred Wegener Institute,BREMERHAVEN, Germany2 Leibniz Institute for Age Research, JENA,GermanyPrymnesium parvum is a toxichaptophyte, which forms harmfulblooms causing mass fishmortalities in brackish and marinewaters. A functi<strong>on</strong>al genomicapproach, within the EU projectESTTAL (expressed sequence tagsof toxic algae), is being used toinvestigate the basis of toxicity andgrowth regulati<strong>on</strong> in this species.About 9,000 cl<strong>on</strong>es randomlyselected from a normalized cDNAlibrary were sequenced andapproximately 15,000 ESTs havebeen generated. The resulting~6230 c<strong>on</strong>tigs were analysed insilico and classified into functi<strong>on</strong>alcategories. The ESTs served as thebasis for olig<strong>on</strong>ucleotide design toproduce a microarray for geneexpressi<strong>on</strong> analysis. Prymnesiumtoxins, known as prymnesins, arelinear polyether compoundssuggesting that are produced or at134

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