Laboratory of Pathology and Immunology of Aquatic Animals, Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, 5 Yushan Road, Qingdao 266003, China.
Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China.
Int J Mol Sci. 2018 Jan 5;19(1):160. doi: 10.3390/ijms19010160.
Lymphocystis disease virus (LCDV) infection may induce a variety of host gene expression changes associated with disease development; however, our understanding of the molecular mechanisms underlying host-virus interactions is limited. In this study, RNA sequencing (RNA-seq) was employed to investigate differentially expressed genes (DEGs) in the gill of the flounder () at one week post LCDV infection. Transcriptome sequencing of the gill with and without LCDV infection was performed using the Illumina HiSeq 2500 platform. In total, RNA-seq analysis generated 193,225,170 clean reads aligned with 106,293 unigenes. Among them, 1812 genes were up-regulated and 1626 genes were down-regulated after LCDV infection. The DEGs related to cellular process and metabolism occupied the dominant position involved in the LCDV infection. A further function analysis demonstrated that the genes related to inflammation, the ubiquitin-proteasome pathway, cell proliferation, apoptosis, tumor formation, and anti-viral defense showed a differential expression. Several DEGs including , toll-like receptors, cytokine-related genes, antiviral related genes, and apoptosis related genes were involved in LCDV entry and immune response. In addition, RNA-seq data was validated by quantitative real-time PCR. For the first time, the comprehensive gene expression study provided valuable insights into the host-pathogen interaction between flounder and LCDV.
淋巴囊肿病病毒 (LCDV) 感染可能会引起宿主基因表达的多种变化,这些变化与疾病的发展有关;然而,我们对宿主-病毒相互作用的分子机制的理解是有限的。在这项研究中,采用 RNA 测序 (RNA-seq) 技术研究了在 LCDV 感染后一周的牙鲆 () 鳃中差异表达基因 (DEGs)。使用 Illumina HiSeq 2500 平台对感染和未感染 LCDV 的牙鲆鳃进行了转录组测序。总共,RNA-seq 分析生成了 193,225,170 条与 106,293 个基因簇匹配的清洁读段。其中,LCDV 感染后有 1812 个基因上调,1626 个基因下调。与细胞过程和代谢相关的 DEGs 在涉及 LCDV 感染的过程中占据主导地位。进一步的功能分析表明,与炎症、泛素-蛋白酶体途径、细胞增殖、凋亡、肿瘤形成和抗病毒防御相关的基因表现出差异表达。几个 DEGs,包括 、toll 样受体、细胞因子相关基因、抗病毒相关基因和凋亡相关基因,参与了 LCDV 的进入和免疫反应。此外,通过定量实时 PCR 验证了 RNA-seq 数据。本研究首次对牙鲆与 LCDV 之间的宿主-病原体相互作用进行了全面的基因表达研究,为深入了解该领域提供了有价值的见解。