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利用生态毒理学基因组学解析紫外光过滤剂(二苯甲酮-3)和高温对软珊瑚 Acropora tenuis 产生的不良影响的作用机制。

Deciphering mechanisms of UV filter (benzophenone-3)- and high temperature-induced adverse effects in the coral Acropora tenuis, using ecotoxicogenomics.

机构信息

R&D Safety Science Research, Kao Corporation, 2606 Akabane, Ichikai-Machi, Haga-Gun, Tochigi, Japan.

Atmosphere and Ocean Research Institute, The University of Tokyo, Kashiwa, Chiba, Japan; Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Chiba, Japan.

出版信息

Sci Total Environ. 2024 Dec 1;954:176018. doi: 10.1016/j.scitotenv.2024.176018. Epub 2024 Sep 13.

DOI:10.1016/j.scitotenv.2024.176018
PMID:39278489
Abstract

Coral reefs are at risk of bleaching due to various environmental and anthropogenic stressors such as global warming and chemical pollutants. However, there is little understanding of stressor-specific mechanisms that cause coral bleaching. Therefore, conducting accurate ecotoxicological risk assessments and deciphering modes of action of potentially deleterious ultraviolet (UV) filters (sunscreen compounds) are crucial issues. In this study, we evaluated the toxicity and bleaching effect of benzophenone-3 (BP-3), which is widely used in sunscreen products, on the reef-building coral Acropora tenuis. Furthermore, to understand differences in UV filter- and temperature-induced adverse effects, a comparative ecotoxicogenomic approach using RNA-seq was integrated into a toxicity test to clarify differences in gene expression changes induced by BP-3 and heat stress (31 °C). The lethal concentration 50 % (LC50) was calculated as 3.9 mg/L, indicating that the aquatic environmental risk on corals posed by BP-3 was low based on the risk assessment in this study. Differentially expressed genes related to oxidative stress and extracellular matrix organization were involved in coral responses to both BP-3 and heat stress, but their patterns differed. Whereas immune and heat-shock responses were activated in response to heat stress, activation of a drug metabolism pathway and several signal transduction pathways were identified in BP-3 treatment groups. Our study enhances understanding of stress responses in corals induced by UV filters and thermal stress. Using potential gene markers identified in this study for eco-epidemiological surveys of stressed corals, we urgently need to develop effective countermeasures.

摘要

珊瑚礁由于全球变暖和化学污染物等各种环境和人为胁迫因素而面临白化风险。然而,对于导致珊瑚白化的胁迫特异性机制知之甚少。因此,进行准确的生态毒理学风险评估和解密潜在有害紫外线 (UV) 过滤器(防晒霜化合物)的作用模式是至关重要的问题。在这项研究中,我们评估了广泛用于防晒霜产品的二苯甲酮-3 (BP-3) 的毒性和白化效应,对造礁珊瑚 Acropora tenuis 的影响。此外,为了了解 UV 滤光片和温度引起的不良影响的差异,我们采用 RNA-seq 进行了比较生态毒理基因组学方法,将其整合到毒性测试中,以阐明 BP-3 和热应激(31°C)引起的基因表达变化的差异。致死浓度 50%(LC50)计算为 3.9 mg/L,表明根据本研究中的风险评估,BP-3 对珊瑚的水生环境风险较低。与氧化应激和细胞外基质组织相关的差异表达基因参与了珊瑚对 BP-3 和热应激的反应,但它们的模式不同。尽管热应激会激活免疫和热休克反应,但在 BP-3 处理组中鉴定到药物代谢途径和几种信号转导途径的激活。我们的研究增强了对 UV 滤光片和热应激引起的珊瑚应激反应的理解。使用本研究中确定的潜在基因标记,对受胁迫的珊瑚进行生态流行病学调查,我们迫切需要制定有效的对策。

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