Laboratory of Radioecology and Ecotoxicology, Institute of Radioprotection and Nuclear Safety, Bd 186, BP 3, 13115 Saint-Paul-Lez-Durance, France.
Ecotoxicol Environ Saf. 2011 Oct;74(7):1800-7. doi: 10.1016/j.ecoenv.2011.06.010. Epub 2011 Jul 8.
This work aims to investigate the accumulation levels and effects (transcriptional responses, histopathology and survival rate) associated with a wide range of dissolved uranium (U) concentrations (0, 0.03, 0.6, 4 and 8 mg/L of U) on adult male crayfish Procambarus clarkii during 4 (T4) and 10 (T10) days of exposure. The follow-up of the crayfish mortality showed that P. clarkii was highly resistant to U. Increasing waterborne U concentrations led to increasing bioaccumulation in key crayfish organs and increasing histological damages. U distribution in tissues was also evaluated using transmission electron microscopy and showed the presence of a detoxified form of U in the gill's epithelium in the shape of flakes. Expression levels of mitochondrial genes (cox1, atp6 and 12S gene) and genes involved in oxidative stress (sod(Mn) and mt) were examined together with the housekeeping gene 18S. atp6 and mt genes of P. clarkii were cloned and sequenced before analysis. Significant correlations were observed between U bioaccumulation and the down-regulation of both cox1 and sod(Mn) genes. This work provides a first U toxicogenomic and histopathological pattern of P. clarkii, identify U biomarkers and associate gene expression endpoints to accumulation levels. It also provides new insights into the mechanisms involved in U stress.
本研究旨在探究成年雄性克氏原螯虾(Procambarus clarkii)在暴露于不同浓度溶解态铀(U)(0、0.03、0.6、4 和 8 mg/L)4 天(T4)和 10 天(T10)后的 U 积累水平及其影响(转录反应、组织病理学和存活率)。通过对克氏原螯虾死亡率的跟踪观察,发现其对 U 具有很强的抗性。随水中 U 浓度的增加,U 在关键螯虾器官中的生物积累增加,组织学损伤加剧。采用透射电子显微镜评估了 U 在组织中的分布,结果显示在鳃上皮细胞中存在一种以薄片形式存在的 U 解毒形式。同时检测了与线粒体相关的基因(cox1、atp6 和 12S 基因)和参与氧化应激的基因(sod(Mn)和 mt)以及管家基因 18S 的表达水平。在分析之前,对 P. clarkii 的 atp6 和 mt 基因进行了克隆和测序。U 的生物积累与 cox1 和 sod(Mn)基因的下调呈显著正相关。本研究为 P. clarkii 的 U 毒性基因组学和组织病理学模式提供了初步认识,鉴定了 U 生物标志物,并将基因表达终点与积累水平联系起来。同时,本研究还为 U 应激相关机制提供了新的见解。