Zhou Zhi, Zhao Shuimiao, Tang Jia, Liu Zhaoqun, Wu Yibo, Wang Yan, Lin Senjie
Key Laboratory of Tropical Biological Resources of Ministry of Education, Hainan University, Haikou, China.
Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian, China.
Front Physiol. 2019 Apr 2;10:366. doi: 10.3389/fphys.2019.00366. eCollection 2019.
is known to cause coral diseases, especially under environmental perturbation, but its impact on coral physiology and underpinning mechanism is poorly understood. In the present study, we investigated cytological, immunological, and metatranscriptomic responses of the scleractinian coral to infection. The density and chlorophyll content of symbiotic zooxanthellae decreased significantly at 12 and 24 h after challenge. The activities of antioxidant enzymes such as superoxide dismutase and catalase, nitric oxide synthase, phenoloxidase (PO), and the activation level of caspase3 all rose significantly in after challenge. In the metatranscriptomic analysis, we found 10 significantly upregulated genes in the symbionts at 24 h after the challenge, which were mostly involved in the metabolism of nucleic acid and polysaccharide, and 133 significantly down-regulated symbiont genes, which were mainly related to amino acid catabolism and transport. Meanwhile, 1432 significantly upregulated coral genes were revealed, highly overrepresented in GO terms that are mostly related to the regulation of immune response, the regulation of cytokine production, and innate immune response. Furthermore, at 24 h after challenge, 890 coral genes were significantly downregulated, highly overrepresented in four GO terms implicated in defense response. These results in concert suggest that infection triggered the innate immune response including the redox, PO, and apoptosis systems, but repressed the response of the complement system in the scleractinian coral , accompanied by symbiont density decrease and symbiosis collapse through disordering the metabolism of the symbionts. These findings shed light on the molecular regulatory processes underlying bleaching and degradation of resulting from the infection of .
已知其会引发珊瑚疾病,尤其是在环境扰动的情况下,但其对珊瑚生理学及潜在机制的影响却知之甚少。在本研究中,我们调查了石珊瑚对感染的细胞学、免疫学和宏转录组学反应。在受到攻击后的12小时和24小时,共生虫黄藻的密度和叶绿素含量显著下降。攻击后,超氧化物歧化酶、过氧化氢酶、一氧化氮合酶、酚氧化酶(PO)等抗氧化酶的活性以及caspase3的激活水平均显著上升。在宏转录组分析中,我们发现在攻击后24小时,共生体中有10个基因显著上调,这些基因大多参与核酸和多糖的代谢,还有133个共生体基因显著下调,主要与氨基酸分解代谢和转运有关。同时,发现有1432个珊瑚基因显著上调,在与免疫反应调节、细胞因子产生调节和先天免疫反应相关的基因本体(GO)术语中高度富集。此外,在攻击后24小时,890个珊瑚基因显著下调,在与防御反应相关的四个GO术语中高度富集。这些结果共同表明,感染引发了包括氧化还原、PO和凋亡系统在内的先天免疫反应,但抑制了石珊瑚中补体系统的反应,同时通过扰乱共生体的代谢导致共生体密度降低和共生关系崩溃。这些发现揭示了由感染导致的珊瑚白化和退化背后的分子调控过程。