Anderson David A, Walz Marcus E, Weil Ernesto, Tonellato Peter, Smith Matthew C
Department of Pathology and Immunology, Washington University in St. Louis, St. Louis, Missouri, United States of America; Department of Marine Sciences, University of Puerto Rico at Mayagüez, Mayagüez, Puerto Rico, United States of America.
Joseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee , Milwaukee, Wisconsin , United States of America.
PeerJ. 2016 Feb 15;4:e1616. doi: 10.7717/peerj.1616. eCollection 2016.
Climate change-driven coral disease outbreaks have led to widespread declines in coral populations. Early work on coral genomics established that corals have a complex innate immune system, and whole-transcriptome gene expression studies have revealed mechanisms by which the coral immune system responds to stress and disease. The present investigation expands bioinformatic data available to study coral molecular physiology through the assembly and annotation of a reference transcriptome of the Caribbean reef-building coral, Orbicella faveolata. Samples were collected during a warm water thermal anomaly, coral bleaching event and Caribbean yellow band disease outbreak in 2010 in Puerto Rico. Multiplex sequencing of RNA on the Illumina GAIIx platform and de novo transcriptome assembly by Trinity produced 70,745,177 raw short-sequence reads and 32,463 O. faveolata transcripts, respectively. The reference transcriptome was annotated with gene ontologies, mapped to KEGG pathways, and a predicted proteome of 20,488 sequences was generated. Protein families and signaling pathways that are essential in the regulation of innate immunity across Phyla were investigated in-depth. Results were used to develop models of evolutionarily conserved Wnt, Notch, Rig-like receptor, Nod-like receptor, and Dicer signaling. O. faveolata is a coral species that has been studied widely under climate-driven stress and disease, and the present investigation provides new data on the genes that putatively regulate its immune system.
气候变化引发的珊瑚疾病暴发已导致珊瑚种群数量普遍下降。早期关于珊瑚基因组学的研究表明,珊瑚拥有复杂的固有免疫系统,全转录组基因表达研究揭示了珊瑚免疫系统应对压力和疾病的机制。本研究通过对加勒比造礁珊瑚奥氏蜂巢珊瑚(Orbicella faveolata)的参考转录组进行组装和注释,扩展了用于研究珊瑚分子生理学的生物信息数据。样本于2010年在波多黎各的一次暖水热异常、珊瑚白化事件和加勒比黄带病暴发期间采集。在Illumina GAIIx平台上对RNA进行多重测序,并通过Trinity进行转录组从头组装,分别产生了70,745,177条原始短序列读数和32,463条奥氏蜂巢珊瑚转录本。参考转录组用基因本体进行注释,映射到KEGG通路,并生成了一个包含20,488个序列的预测蛋白质组。对跨门固有免疫调节中至关重要的蛋白质家族和信号通路进行了深入研究。研究结果用于构建进化上保守的Wnt、Notch、RIG样受体、NOD样受体和Dicer信号通路模型。奥氏蜂巢珊瑚是一种在气候驱动的压力和疾病下受到广泛研究的珊瑚物种,本研究提供了关于可能调节其免疫系统的基因的新数据。