Marine Science Center, Northeastern University, Nahant, Massachusetts, United States of America.
PLoS One. 2013 Nov 21;8(11):e81821. doi: 10.1371/journal.pone.0081821. eCollection 2013.
Coral diseases are among the most serious threats to coral reefs worldwide, yet most coral diseases remain poorly understood. How the coral host responds to pathogen infection is an area where very little is known. Here we used next-generation RNA-sequencing (RNA-seq) to produce a transcriptome-wide profile of the immune response of the Staghorn coral Acropora cervicornis to White Band Disease (WBD) by comparing infected versus healthy (asymptomatic) coral tissues. The transcriptome of A. cervicornis was assembled de novo from A-tail selected Illumina mRNA-seq data from whole coral tissues, and parsed bioinformatically into coral and non-coral transcripts using existing Acropora genomes in order to identify putative coral transcripts. Differentially expressed transcripts were identified in the coral and non-coral datasets to identify genes that were up- and down-regulated due to disease infection. RNA-seq analyses indicate that infected corals exhibited significant changes in gene expression across 4% (1,805 out of 47,748 transcripts) of the coral transcriptome. The primary response to infection included transcripts involved in macrophage-mediated pathogen recognition and ROS production, two hallmarks of phagocytosis, as well as key mediators of apoptosis and calcium homeostasis. The strong up-regulation of the enzyme allene oxide synthase-lipoxygenase suggests a key role of the allene oxide pathway in coral immunity. Interestingly, none of the three primary innate immune pathways--Toll-like receptors (TLR), Complement, and prophenoloxydase pathways, were strongly associated with the response of A. cervicornis to infection. Five-hundred and fifty differentially expressed non-coral transcripts were classified as metazoan (n = 84), algal or plant (n = 52), fungi (n = 24) and protozoans (n = 13). None of the 52 putative Symbiodinium or algal transcript had any clear immune functions indicating that the immune response is driven by the coral host, and not its algal symbionts.
珊瑚疾病是全球范围内对珊瑚礁最严重的威胁之一,但大多数珊瑚疾病仍知之甚少。珊瑚宿主对病原体感染的反应是一个知之甚少的领域。在这里,我们使用下一代 RNA 测序(RNA-seq)通过比较感染和健康(无症状)珊瑚组织,生成鹿角珊瑚 Acropora cervicornis 对白色带疾病(WBD)的免疫反应的全转录组图谱。从 A 尾选择的 Illumina mRNA-seq 数据从头组装 A. cervicornis 的转录组,并使用现有的 Acropora 基因组在生物信息学上解析为珊瑚和非珊瑚转录本,以鉴定推定的珊瑚转录本。在珊瑚和非珊瑚数据集之间鉴定差异表达的转录本,以鉴定因疾病感染而上调或下调的基因。RNA-seq 分析表明,感染的珊瑚在 4%(47748 个转录本中的 1805 个)的珊瑚转录本中表现出显著的基因表达变化。感染的主要反应包括涉及巨噬细胞介导的病原体识别和 ROS 产生的转录本,这是吞噬作用的两个标志,以及凋亡和钙稳态的关键介质。烯氧合酶-脂氧合酶的强烈上调表明该途径在珊瑚免疫中具有关键作用。有趣的是,三个人先天免疫途径——Toll 样受体(TLR)、补体和酚氧化酶途径——都没有与 A. cervicornis 对感染的反应强烈相关。550 个差异表达的非珊瑚转录本被归类为后生动物(n = 84)、藻类或植物(n = 52)、真菌(n = 24)和原生动物(n = 13)。52 个推定的 Symbiodinium 或藻类转录本都没有明显的免疫功能,这表明免疫反应是由珊瑚宿主驱动的,而不是其藻类共生体。