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Revealing Holobiont Structure and Function of Three Red Sea Deep-Sea Corals

机译:揭示三种红海深海珊瑚的Holobiont结构和功能

摘要

Deep-sea corals have long been regarded as cold-water coral; however a reevaluationof their habitat limitations has been suggested after the discovery ofdeep-sea coral in the Red Sea where temperatures exceed 20˚C. To gain furtherinsight into the biology of deep-sea corals at these temperatures, the work in thisPhD employed a holotranscriptomic approach, looking at coral animal host andbacterial symbiont gene expression in Dendrophyllia sp., Eguchipsammia fistula, andRhizotrochus sp. sampled from the deep Red Sea. Bacterial community compositionwas analyzed via amplicon-based 16S surveys and cultured bacterial strains weresubjected to bioprospecting in order to gauge the pharmaceutical potential of coralassociatedmicrobes.Coral host transcriptome data suggest that coral can employ mitochondrialhypometabolism, anaerobic glycolysis, and surface cilia to enhance mass transportrates to manage the low oxygen and highly oligotrophic Red Sea waters. In themicrobial community associated with these corals, ribokinases and retron-typereverse transcriptases are abundantly expressed. In its first application to deep-seacoral associated microbial communities, 16S-based next-generation sequencingfound that a single operational taxonomic unit can comprise the majority ofsequence reads and that a large number of low abundance populations are present,which cannot be visualized with first generation sequencing. Bioactivity testing ofselected bacterial isolates was surveyed over 100 cytological parameters with high content screening, covering several major organelles and key proteins involved in avariety of signaling cascades. Some of these cytological profiles were similar tothose of several reference pharmacologically active compounds, which suggest thatthe bacteria isolates produce compounds with similar mechanisms of action as thereference compounds.The sum of this work offers several mechanisms by which Red Sea deep-sea coralscope with environmental conditions in which no other deep-sea corals have yet tobe reported. These deep-sea coral are associated with rich microbial communities,which produce molecules that induce bioactivity. The aggregate of this workprovides direction for future research of Red Sea deep-sea coral and highlights thepotential pharmacological benefit of conserving these species and their uniqueecosystem.
机译:深海珊瑚长期以来被认为是冷水珊瑚。然而,在温度超过20 temperaturesC的红海中发现深海珊瑚后,建议重新评估其栖息地的限制。为了进一步了解在这样的温度下深海珊瑚的生物学特性,本博士论文采用了全基因组方法,研究了Dendrophyllia sp。,Eguchipsammia fistula和Rhizotrochus sp。中的珊瑚动物宿主和细菌共生基因表达。从深红海采样。通过基于扩增子的16S调查分析细菌群落组成,并对培养的细菌菌株进行生物勘探,以评估珊瑚相关微生物的药物潜力。珊瑚宿主转录组数据表明,珊瑚可以利用线粒体低代谢,厌氧糖酵解和表面纤毛来增强传质来管理。低氧和富营养化的红海水。在与这些珊瑚有关的微生物群落中,核糖激酶和逆转录型逆转录酶大量表达。基于16S的下一代测序技术在首次应用于深海珊瑚相关微生物群落时,发现单个操作生物分类单元可构成大多数序列读数,并且存在大量低丰度种群,而第一代种群无法观察到排序。选定的细菌分离物的生物活性测试通过高内涵筛选进行了100多个细胞学参数的调查,涵盖了涉及信号级联多样性的几种主要细胞器和关键蛋白。这些细胞学特征中的一些与几种参考药理活性化合物的细胞学特征相似,这表明细菌分离物产生与参考化合物具有相似作用机理的化合物。这项工作的总和提供了几种在环境条件下红海深海珊瑚镜的机理。其中尚无其他深海珊瑚的报道。这些深海珊瑚与丰富的微生物群落有关,微生物群落产生诱导生物活性的分子。这项工作的总和为红海深海珊瑚的未来研究提供了方向,并强调了保护这些物种及其独特生态系统的潜在药理学益处。

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