Institute of Aquatic Biology and Jiangsu Key Laboratory for Biofunctional Molecules, College of Life Sciences and Chemistry, Jiangsu Second Normal University, Nanjing, People's Republic of China.
State Key Laboratory Breeding Base of Marine Genetic Resource, Third Institute of Oceanography, SOA, Xiamen, People's Republic of China.
PLoS One. 2018 Sep 28;13(9):e0204626. doi: 10.1371/journal.pone.0204626. eCollection 2018.
Intestine is a primary site of the white spot syndrome virus (WSSV) infection in most crustaceans. To date, little is known about its role in the anti-viral immune response in the freshwater prawn Macrobrachium rosenbergii. In this study, next-generation sequencing was employed to investigate the M. rosenbergii intestine transcriptomes following WSSV or poly I:C challenges. A total of 41.06 M, 39.58 M and 47.00 M clean reads were generated and assembled into 65,340, 71,241 and 70,614 transcripts from the negative control group (NG), WSSV challenge group (WG) and poly I:C treatment group (PG) respectively. Based on homology searches, functional annotation with 7 databases (NR, NT, GO, COG, KEGG, Swissprot and Interpro) for 88,412 transcripts was performed. After WSSV or poly (I:C) challenge, the numbers of up-regulated differentially expressed genes (DEGs) were greater than the down-regulated DEGs. Gene Ontology (GO) classification of the DEGs also distributed similarly, with the same top 10 annotations and were all assigned to the signaling pathways, including spliceosome, Rap1 signaling pathway, proteoglycans, PI3K-Akt signaling pathway, ECM receptor interaction. Results could contribute to a better understanding of the intestinal immune response to viral pathogens.
肠是大多数甲壳类动物中白斑综合征病毒(WSSV)感染的主要部位。迄今为止,人们对其在淡水虾罗氏沼虾抗病毒免疫反应中的作用知之甚少。在这项研究中,采用下一代测序技术研究了 WSSV 或多聚 I:C 挑战后罗氏沼虾肠转录组。从阴性对照组(NG)、WSSV 攻毒组(WG)和多聚 I:C 处理组(PG)分别生成了 41.06 M、39.58 M 和 47.00 M 的清洁读数,并组装成 65340、71241 和 70614 个转录本。基于同源搜索,对 7 个数据库(NR、NT、GO、COG、KEGG、Swissprot 和 Interpro)的 88412 个转录本进行了功能注释。在 WSSV 或多聚(I:C)攻毒后,上调的差异表达基因(DEG)的数量大于下调的 DEG。DEG 的基因本体论(GO)分类也分布相似,前 10 个注释相同,均被分配到信号通路,包括剪接体、Rap1 信号通路、蛋白聚糖、PI3K-Akt 信号通路、ECM 受体相互作用。结果有助于更好地了解肠道对病毒病原体的免疫反应。