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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 2006PO.05-07Testing of a passive adsorpti<strong>on</strong>device in the detecti<strong>on</strong> of DTXsunder c<strong>on</strong>trolled c<strong>on</strong>diti<strong>on</strong>sSessi<strong>on</strong>: PO.05 - Toxin analysisClaire Marcaillou, Florence M<strong>on</strong>deguer,Jean Bapt Bérard, Amélie GoupilIFREMER, NANTES, FranceRecently, McKenzie and hiscollaborators described an attractivetechnique to detect lipophilic toxinsin the field. The principle is based<strong>on</strong> the passive adsorpti<strong>on</strong> of toxins<strong>on</strong>to porous synthetic resin held insmall bags. For the purpose ofusing this technique for adec<strong>on</strong>taminati<strong>on</strong> trial, anexperiment was set up in thelaboratory with a Prorocentrum limaculture. Prorcentrum lima is abenthic species producing DTXsand cultivable in the laboratory. Thecumulative adsorpti<strong>on</strong> was studiedunder three envir<strong>on</strong>mentalc<strong>on</strong>diti<strong>on</strong>s: in the raw culture, in thefiltrate and in the lysate of the sameculture. The results obtained fromthis preliminary experiment were asfollows: the cumulative adsorpti<strong>on</strong>does not seem to be modified bythe cell presence, its relati<strong>on</strong>shipwith exposure time is linear overtime and for the toxin levels studied,and the reproducibility is good in allcases.PO.15-16The Envir<strong>on</strong>mental SampleProcessor (ESP): a robotic devicefor detecting microorganismsremotely using molecular probetechnologySessi<strong>on</strong>: PO.15 - M<strong>on</strong>itoringR Marin III 1 , C Scholin 1 , S Jensen 1 , BRoman 1 , J Feldman 2 , D Greenfield 1 , CPrest<strong>on</strong> 1 , W J<strong>on</strong>es 1 , E Massi<strong>on</strong> 1 , GDoucette 3 , T Mikulski 31 MBARI, MOSS LANDING, CA, UnitedStates of America2 Jet Propulsi<strong>on</strong> Labaratory, PASADENA,CA, United States of America3 Marine Biotoxins Program, NOAA/NOS,CHARLESTON, SC, United States ofAmericaOne of our primary research goalsis to develop analytical techniquesand instrumentati<strong>on</strong> that allow us touse molecular probe technology todetect microorganisms, their genesand gene products remotely, in situ.Towards that end we havedeveloped the ESP,http://www.mbari.org/microbial/ESP,a device designed to collect discretewater samples from the oceansubsurface, c<strong>on</strong>centrateparticulates, and automateapplicati<strong>on</strong> of ribosomal RNA(rRNA) targeted DNA probe arrays(see Greenfield et al.) and antibodybaseddiagnostics (see Doucette etal.). The ESP can also be used toarchive samples for a variety ofnucleic acid analyses, microscopyand other types of analyticalprocedures after the instrument isrecovered. To date, 3 differentclasses of DNA probe arrays thattarget a variety of bacteria andarchaea, harmful algae, and larvalinvertebrates have been applied insingle field deployments inM<strong>on</strong>terey Bay, CA, lasting ~20 d. Inc<strong>on</strong>cert with the probe arrays fordetecting a suite of HAB speciesthat include Pseudo-nitzschiaaustralis, P. multiseries and P.pseudodelicatissima, we havesuccessfully utilized a competitiveELISA technique for detectingdomoic acid. In this presentati<strong>on</strong> wewill review the design and workingsof the ESP, and our plans for futuredeployments, developments andtechnology transfer.232

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