Laboratory of Fish Diseases, Department of Aquaculture, Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, PR China; Heilongjiang Key Laboratory of Breeding and Aquaculture of Cold-water Fish, Harbin 150070, PR China.
Laboratory of Fish Diseases, Department of Aquaculture, Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, PR China.
Fish Shellfish Immunol. 2017 Nov;70:451-460. doi: 10.1016/j.fsi.2017.09.033. Epub 2017 Sep 13.
Yersinia ruckeri (YR) is the causative agent of yersiniosis which has caused significant economic losses in fish culture worldwide, including in Amur sturgeon (Acipenser schrenckii) culture. To better understand the mechanism of the immune responses to YR in Amur sturgeon, the transcriptomic profiles of the spleens from YR-infected and non-infected groups were obtained using RNA-seq techniques. The de novo assemblies yielded totally 145 670 unigenes from the two libraries. The total numbers of transcripts in YR-infected and non-infected groups were from 110 893 to 147 336, with the mean length varying from 560 to 631 (N50: from 882 to 1083). GO analysis revealed that 10 038 unigenes were categorized into 26 biological processes subcategories, 17 cellular components subcategories and 19 molecular functions subcategories. A total of 59 487 unigenes were annotated in the KEGG pathway and 20 pathways were related to the immune system. 1465 differently expressed genes (DEGs) were identified, including 377 up-regulated genes and 1088 down-regulated genes. 125 DEGs were found to be related to immune responses of Amur sturgeon and further divided into 16 immune-related KEGG pathways, including antigen processing and presentation, complement and coagulation cascades, T cell receptor signaling pathway, B cell receptor signaling pathway, NOD-like receptor signaling pathway, chemokine signaling pathway, etc. Eight of the DEGs were further validated by qRT-PCR. Altogether, the results obtained in this study will provide insight into the immune response of Amur sturgeon against Y. ruckeri infection.
豚鼠气单胞菌(YR)是鱼类疾病弧菌病的病原体,在全球鱼类养殖中造成了重大经济损失,包括在鲟鱼养殖中。为了更好地了解鲟鱼对 YR 免疫反应的机制,本研究采用 RNA-seq 技术获得了 YR 感染和未感染组脾脏的转录组图谱。从头组装总共从两个文库中获得了 145670 个基因。YR 感染组和未感染组的转录本总数从 110893 到 147336 不等,平均长度从 560 到 631(N50:从 882 到 1083)。GO 分析表明,10038 个基因被分为 26 个生物过程亚类、17 个细胞成分亚类和 19 个分子功能亚类。总共 59487 个基因在 KEGG 途径中被注释,其中 20 个途径与免疫系统有关。鉴定出 1465 个差异表达基因(DEGs),包括 377 个上调基因和 1088 个下调基因。发现 125 个 DEGs 与鲟鱼的免疫反应有关,并进一步分为 16 个与免疫有关的 KEGG 途径,包括抗原加工和呈递、补体和凝血级联、T 细胞受体信号通路、B 细胞受体信号通路、NOD 样受体信号通路、趋化因子信号通路等。其中 8 个 DEGs 通过 qRT-PCR 进一步验证。总之,本研究结果将为了解鲟鱼对 Y. ruckeri 感染的免疫反应提供新的视角。