Collaborative study for the detection of toxic compounds in shellfish extracts using cell-based assays. Part I: screening strategy and pre-validation study with lipophilic marine toxins

被引:0
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作者
Anne-Laure Sérandour
Aurélie Ledreux
Bénédicte Morin
Sylvain Derick
Elie Augier
Rachelle Lanceleur
Sahima Hamlaoui
Serge Moukha
Christophe Furger
Ronel Biré
Sophie Krys
Valérie Fessard
Marc Troussellier
Cécile Bernard
机构
[1] Unité de Toxicologie des Contaminants,UMR 7245 MNHN
[2] ANSES,CNRS MCAM
[3] Muséum National d’Histoire Naturelle,Laboratoire de Toxicologie
[4] UMR 5805 Université Bordeaux 1-CNRS EPOC,undefined
[5] LPTC,undefined
[6] Novaleads,undefined
[7] Université Bordeaux Segalen-INRA,undefined
[8] Unité de Caractérisation des Toxines,undefined
[9] ANSES,undefined
[10] UMR 5119 ECOSYM Université Montpellier 2 & 1-CNRS-IRD-Ifremer,undefined
来源
Analytical and Bioanalytical Chemistry | 2012年 / 403卷
关键词
Cell-based assays; Collaborative study; Lipophilic phycotoxins; Cytotoxicity;
D O I
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学科分类号
摘要
Human poisoning due to consumption of seafood contaminated with phycotoxins is a worldwide problem, and routine monitoring programs have been implemented in various countries to protect human consumers. Following successive episodes of unexplained shellfish toxicity since 2005 in the Arcachon Bay on the French Atlantic coast, a national research program was set up to investigate these atypical toxic events. Part of this program was devoted to fit-for-purpose cell-based assays (CBA) as complementary tools to collect toxicity data on atypical positive-mouse bioassay shellfish extracts. A collaborative study involving five laboratories was conducted. The responses of human hepatic (HepG2), human intestinal (Caco2), and mouse neuronal (Neuro2a) cell lines exposed to three known lipophilic phycotoxins—okadaic acid (OA), azaspiracid-1 (AZA1), and pectenotoxin-2 (PTX2)—were investigated. A screening strategy composed of standard operating procedures and a decision tree for dose–response modeling and assay validation were designed after a round of “trial-and-error” process. For each toxin, the shape of the concentration–response curves and the IC50 values were determined on the three cell lines. Whereas OA induced a similar response irrespective of the cell line (complete sigmoid), PTX2 was shown to be less toxic. AZA1 induced cytotoxicity only on HepG2 and Neuro2a, but not on Caco2. Intra- and inter-laboratory coefficients of variation of cell responses were large, with mean values ranging from 35 to 54 % and from 37 to 48 %, respectively. Investigating the responses of the selected cell lines to well-known toxins is the first step supporting the use of CBA among the panel of methods for characterizing atypical shellfish toxicity. Considering these successful results, the CBA strategy will be further applied to extracts of negative, spiked, and naturally contaminated shellfish tissues.
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页码:1983 / 1993
页数:10
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共 9 条
  • [1] Collaborative study for the detection of toxic compounds in shellfish extracts using cell-based assays. Part I: screening strategy and pre-validation study with lipophilic marine toxins
    Serandour, Anne-Laure
    Ledreux, Aurelie
    Morin, Benedicte
    Derick, Sylvain
    Augier, Elie
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    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2012, 403 (07) : 1983 - 1993
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