Dong Ying, Sun Hongjuan, Zhou Zunchun, Yang Aifu, Chen Zhong, Guan Xiaoyan, Gao Shan, Wang Bai, Jiang Bei, Jiang Jingwei
Liaoning Key Lab of Marine Fishery Molecular Biology, Liaoning Ocean and Fisheries Science Research Institute, Dalian 116023, China.
Int J Mol Sci. 2014 Oct 27;15(11):19472-86. doi: 10.3390/ijms151119472.
The sea cucumber (Apostichopus japonicus) occupies a basal position during the evolution of deuterostomes and is also an important aquaculture species. In order to identify more immune effectors, transcriptome sequencing of A. japonicus coelomocytes in response to lipopolysaccharide (LPS) challenge was performed using the Illumina HiSeq™ 2000 platform. One hundred and seven differentially expressed genes were selected and divided into four functional categories including pathogen recognition (25 genes), reorganization of cytoskeleton (27 genes), inflammation (41 genes) and apoptosis (14 genes). They were analyzed to elucidate the mechanisms of host-pathogen interactions and downstream signaling transduction. Quantitative real-time polymerase chain reactions (qRT-PCRs) of 10 representative genes validated the accuracy and reliability of RNA sequencing results with the correlation coefficients from 0.88 to 0.98 and p-value <0.05. Expression analysis of immune-related genes after LPS challenge will be useful in understanding the immune response mechanisms of A. japonicus against pathogen invasion and developing strategies for resistant markers selection.
海参(刺参)在后口动物进化过程中处于基础地位,也是一种重要的水产养殖物种。为了鉴定更多的免疫效应分子,利用Illumina HiSeq™ 2000平台对经脂多糖(LPS)刺激的刺参体腔细胞进行了转录组测序。筛选出107个差异表达基因,并分为四个功能类别,包括病原体识别(25个基因)、细胞骨架重组(27个基因)、炎症(41个基因)和凋亡(14个基因)。对这些基因进行分析以阐明宿主 - 病原体相互作用及下游信号转导的机制。10个代表性基因的定量实时聚合酶链反应(qRT-PCR)验证了RNA测序结果的准确性和可靠性,相关系数在0.88至0.98之间,p值<0.05。LPS刺激后免疫相关基因的表达分析将有助于理解刺参抵抗病原体入侵的免疫反应机制,并为抗性标记选择制定策略。