Laboratory of Fish Immunology and Nutrigenomics, Applied Animal and Aquatic Sciences Research Unit, Division of Fisheries, Faculty of Technology, Mahasarakham University, Khamriang Sub-District, Kantarawichai, Mahasarakham, 44150, Thailand.
Applied Taxonomic Research Center, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand; Laboratory of Biodiversity and Environmental Management, International College, Khon Kaen University, Khon Kaen, 40002, Thailand.
Fish Shellfish Immunol. 2022 Feb;121:108-115. doi: 10.1016/j.fsi.2021.12.053. Epub 2022 Jan 1.
To enhance genomic resources and to understand the molecular immune mechanisms underlying the response of fairy shrimp (Streptocephalus sirindhornae) to pathogens, we first performed a comparative gene transcription analysis from Aeromonas hydrophila-immunized shrimp and from a control group through RNA sequencing. Meanwhile, the differentially expressed genes (DEGs) were investigated, and a total of 46,958,894 clean reads were obtained and then assembled into 73,297 unigenes with an average length of 993 bp and an N50 of 1,458 bp. Unigenes were annotated by comparison with the NR/NT/KO/SwissProt/PFAM/GO and KOG databases, and 28,198 unigenes (38.47%) were annotated in at least one database. After a bacterial challenge, 143 and 287 genes were identified as markedly up- or downregulated, respectively, and 345 were associated with 142 pathways, including the classic immune-related apoptosis, toll-like receptor and MAPK signaling pathways. Moreover, ten differently expressed immune-related genes were confirmed by using quantitative real-time PCR. This study characterized a gene expression pattern for normal and Aeromonas hydrophila-immunized S. sirindhornae for the first time and shed new light on its molecular mechanisms, thus enabling the future efforts of disease control programs for this valuable aquaculture species.
为了增强基因组资源,并了解卤虫(Streptocephalus sirindhornae)对病原体反应的分子免疫机制,我们首先通过 RNA 测序对从嗜水气单胞菌免疫的虾和对照组进行了比较基因转录分析。同时,研究了差异表达基因(DEGs),共获得了 4695884 条清洁读数,然后组装成 73297 条 unigenes,平均长度为 993bp,N50 为 1458bp。通过与 NR/NT/KO/SwissProt/PFAM/GO 和 KOG 数据库进行比较,对 unigenes 进行了注释,其中 28198 个 unigenes(38.47%)在至少一个数据库中得到了注释。在细菌攻毒后,分别鉴定出 143 个和 287 个基因显著上调或下调,其中 345 个与 142 个通路相关,包括经典的免疫相关凋亡、Toll 样受体和 MAPK 信号通路。此外,还通过实时定量 PCR 验证了 10 个差异表达的免疫相关基因。本研究首次对正常卤虫和嗜水气单胞菌免疫的卤虫进行了基因表达模式的描述,揭示了其分子机制,从而为该有价值的水产养殖物种的疾病控制计划的未来努力提供了新的思路。