Murphy James W A, Collier Abby C, Richmond Robert H
Kewalo Marine Laboratory, Pacific Biosciences Research Center, University of Hawaii at Manoa, Honolulu, HI, United States of America.
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, Hawaii (HI), United States of America.
PeerJ. 2019 Jun 7;7:e7020. doi: 10.7717/peerj.7020. eCollection 2019.
The impacts of continued degradation of watersheds on coastal coral reefs world-wide is alarming, and action addressing anthropogenic stressors and subsequent rehabilitation of watersheds and adjacent reefs is an urgent priority. The aim of this study is to develop and improve the use of antioxidant enzymes as bioindicators of stress in coral species. In order to fully develop such tools, it is necessary to first understand baseline cycling of these enzymes within coral tissues. Due to inherent links between reproduction and oxidative stress, these aims may be facilitated by sampling coral tissues over reproductively-linked lunar cycles to determine variations from baseline. By developing a greater understanding of biochemical markers of stress in corals, specifically antioxidant defense enzymes catalase (CAT), glutathione reductase (GR), glutathione peroxidase (GPx), and superoxide dismutase (SOD) in Hawaiian , we have provided molecular tools that identify thresholds of stress on coral reefs. Our results suggest that the coral reproductive state is a significant factor affecting the activity of antioxidant enzymes. Specifically, CAT and GR display maximum activity during peak reproductive state. Whereas significant maximal Se-independent GPx and SOD activity was measured during off-peak reproductive cycles. Such insight into the cyclical variation of the activity of these enzymes should be applied towards differentiating the influence of natural biological activity cycling in diagnostic tests identifying the effects of different physical environmental factors and chemical pollutants on coral health. Through the development and application of these molecular biomarkers of stress, we look to improve our ability to identify problems at the sub-lethal level, when action can be taken to mitigate a/biotic impacts.
流域持续退化对全球沿海珊瑚礁的影响令人担忧,应对人为压力源以及随后对流域和邻近珊瑚礁进行恢复的行动是当务之急。本研究的目的是开发并改进将抗氧化酶用作珊瑚物种应激生物指标的方法。为了充分开发此类工具,有必要首先了解这些酶在珊瑚组织内的基线循环情况。由于繁殖与氧化应激之间存在内在联系,通过在与繁殖相关的月周期内对珊瑚组织进行采样以确定与基线的差异,可能有助于实现这些目标。通过更深入地了解珊瑚应激的生化标志物,特别是夏威夷珊瑚中的抗氧化防御酶过氧化氢酶(CAT)、谷胱甘肽还原酶(GR)、谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD),我们提供了可识别珊瑚礁应激阈值的分子工具。我们的结果表明,珊瑚的繁殖状态是影响抗氧化酶活性的一个重要因素。具体而言,CAT和GR在繁殖高峰期表现出最大活性。而在繁殖非高峰期测得显著的最大非硒依赖性GPx和SOD活性。这种对这些酶活性周期性变化的洞察应应用于在诊断测试中区分自然生物活性循环的影响,以确定不同物理环境因素和化学污染物对珊瑚健康的影响。通过开发和应用这些应激分子生物标志物,我们希望提高在亚致死水平识别问题的能力,以便能够采取行动减轻生物/非生物影响。