The comet assay inFolsomia candida: A suitable approach to assess genotoxicity in collembolans

遗传毒性 彗星试验 乐果 琼脂糖 毒理 生物 DNA损伤 溶解 生物测定 DNA 化学 遗传学 分子生物学 杀虫剂 毒性 生态学 有机化学
作者
Diogo N. Cardoso,Ana Rita R. Silva,Andreia Cruz,Joana Lourenço,Joana Neves,Catarina Malheiro,Sónia Mendo,Amadeu M.V.M. Soares,Susana Loureiro
出处
期刊:Environmental Toxicology and Chemistry [Wiley]
卷期号:36 (9): 2514-2520 被引量:11
标识
DOI:10.1002/etc.3795
摘要

The present study shows the comet assay technique being successfully applied for the first time to one of the most widely used soil organisms in standardized ecotoxicological tests, Folsomia candida, providing a step forward in assessing the genotoxicity induced by xenobiotics. Because collembolans have a high content of chitin, a new methodology was developed in which the heads of the collembolans were separated from the rest of the body, allowing the hemolymph to leak out. This procedure allows the cells to be released, and after lysis the genetic material is available for the comet assay. Among other key procedures, the use of 30 organisms (20- to 22-d-old adults) per replicate and the correct amount of cells with genetic material (translated as 10 μL of suspension) applied on the agarose gel were determinants for the success of the results obtained. The methodology was validated by exposing F. candida to a representative metallic element (cadmium) and a representative of organophosphates, the insecticide dimethoate, for a shorter time period of 10 d, compared with the 28 d for the International Organization for Standardization 11267 method. Within this method, the relatively low percentage of DNA damage (30%) observed in controls and the significant increase in terms of percentage of DNA damage for almost all the concentrations of dimethoate and Cd (reaching 52% and 56% of damage in the highest concentrations, respectively) confirmed the genotoxic effect of both compounds and validated this technique. The comet assay proved to be a sensitive technique to detect DNA strand breaks in collembolans' cells. Environ Toxicol Chem 2017;36:2514-2520. © 2017 SETAC.

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