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Dynamics of Protein Phosphatase Gene Expression in Corbicula fluminea Exposed to Microcystin-LR and to Toxic Microcystis aeruginosa Cells

机译:暴露于微囊藻毒素-LR和有毒铜绿微囊藻的Cor杆菌中磷酸酶基因表达的动力学

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摘要

This study investigated the in vivo effects of microcystins on gene expression of several phosphoprotein phosphatases (PPP) in the freshwater clam Corbicula fluminea with two different exposure scenarios. Clams were exposed for 96 h to 5 μg L−1 of dissolved microcystin-LR and the relative changes of gene expression of three different types of PPP (PPP1, 2 and 4) were analyzed by quantitative real-time PCR. The results showed a significant induction of PPP2 gene expression in the visceral mass. In contrast, the cyanotoxin did not cause any significant changes on PPP1 and PPP4 gene expression. Based on these results, we studied alterations in transcriptional patterns in parallel with enzymatic activity of C. fluminea for PPP2, induced by a Microcystis aeruginosa toxic strain (1 × 105 cells cm−3) during 96 h. The relative changes of gene expression and enzyme activity in visceral mass were analyzed by quantitative real-time PCR and colorimetric assays respectively. The clams exhibited a significant reduction of PPP2 activity with a concomitant enhancement of gene expression. Considering all the results we can conclude that the exposure to an ecologically relevant concentration of pure or intracellular microcystins (-LR) promoted an in vivo effect on PPP2 gene expression in C. fluminea.
机译:这项研究调查了微囊藻毒素在两种不同暴露情况下对淡水蛤Cor菌中几种磷蛋白磷酸酶(PPP)基因表达的体内影响。将蛤暴露于5μgL −1 溶解的微囊藻毒素-LR中暴露96小时,并通过定量实时定量分析三种不同类型PPP(PPP1、2和4)的基因表达的相对变化。时间PCR。结果显示在内脏肿块中PPP2基因表达的显着诱导。相反,氰毒素在PPP1和PPP4基因表达上没有引起任何显着变化。基于这些结果,我们研究了由铜绿微囊藻毒性菌株(1×10 5 细胞cm −3 < / sup>),持续96小时。分别通过实时荧光定量PCR和比色法分析内脏组织中基因表达和酶活性的相对变化。蛤显示PPP2活性显着降低,同时基因表达增强。考虑到所有结果,我们可以得出结论,暴露于生态学上相关浓度的纯净或细胞内微囊藻毒素(-LR)可以促进对C. fluminea PPP2基因表达的体内影响。

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