Genotoxicity assessment of pesticides on terrestrial snail embryos by analysis of random amplified polymorphic DNA profiles

Affiliation auteurs!!!! Error affiliation !!!!
TitreGenotoxicity assessment of pesticides on terrestrial snail embryos by analysis of random amplified polymorphic DNA profiles
Type de publicationJournal Article
Year of Publication2015
AuteursBaurand P-E, Capelli N, de Vaufleury A
JournalJOURNAL OF HAZARDOUS MATERIALS
Volume298
Pagination320-327
Date PublishedNOV 15
Type of ArticleArticle
ISSN0304-3894
Mots-clésCopper sulfate, Embryogenotoxicity, Glyphosate, Landsnail, RAPD-HRS, Tebuconazole
Résumé

The study explores the relevance of coupling Random Amplified Polymorphic DNA (RAFD) and a High-Resolution capillary electrophoresis System (HRS) method for assessing the genotoxic potential of the wide variety commercial formulations of pesticides. Using this technique, the genotoxic potential of a glyphosate-based herbicide (Roundup Flash (R) (RU)) and two fungicide formulations based on tebuconazole and copper (Corail (R) and Bordeaux mixture (BM), respectively) was evaluated on terrestrial snail embryos. Clutches of Cantareus aspersus were exposed during their entire embryonic development to a range of concentration around the EC50 values (based on hatching success) for each compound tested. Three primers were used for the RAPD amplifications of pesticides samples. RAPD-HRS revealed concentration-dependent modifications in profiles generated with the three primers in RU (R)-exposed embryos from 30 mg/L glyphosate. For Corair (R)-exposed embryos, only two of the three primers were able to show alterations in profiles from 0.05 mg/L tebuconazole. For BM-exposed embryos, no signs of genotoxicity were observed. All changes observed in amplification profiles have been detected at concentrations lower than the recommended doses for vineyard field applications. Our study demonstrates the efficiency of coupling RAPD and HRS to efficiently screen the effect of pesticide formulations on DNA. (C) 2015 Elsevier B.V. All rights reserved.

DOI10.1016/j.jhazmat.2015.05.051