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中华卤虫对微球菌溶壁亚种感染的转录组分析。

Transcriptome analysis of Artemia sinica in response to Micrococcus lysodeikticus infection.

机构信息

The Key Laboratory of Zoological Systematics and Application, College of Life Sciences, Hebei University, 071002, Baoding, PR China.

The Key Laboratory of Zoological Systematics and Application, College of Life Sciences, Hebei University, 071002, Baoding, PR China.

出版信息

Fish Shellfish Immunol. 2018 Oct;81:92-98. doi: 10.1016/j.fsi.2018.06.033. Epub 2018 Jul 10.

DOI:10.1016/j.fsi.2018.06.033
PMID:30006042
Abstract

To enhance genomic resources and understand the molecular immune mechanisms underlying the response topathogens, we first performed a comparative gene transcription analysis from Micrococcus lysodeikticus-immunized Artemia sinica and from a control group through RNA-Seq technology, meanwhile the differentially expressed genes (DEGs) were investigated. In total, 80, 113, 984 clean reads were obtained and then assembled into 71,536 unigenes with an average length of 1115 bp and an N50 of 1783 bp. Unigenes were annotated by comparing against nr, Swiss-Prot\KEGG\ COG\ KOG\ GO and Pfam databases, and 27,689 unigenes (38.7%) were annotated in at least one database. After bacterial challenge, 183 and 298 genes were identified as remarkably up-regulated or down-regulated, respectively, amongst 481 were associated with 168 pathways, including classical immune-related pathways, such as 'Toll-like receptor signaling', 'the complement cascades', 'MAPK signaling pathway' and 'Apoptosis'. Besides, eight genes which were differently expressed immune-related were confirmed by using quantitative real-time PCR. This study characterized a gene expression pattern for normal and M. lysodeikticus -immunized A. sinica for the first time and sheds new light on the molecular mechanisms thus enabling future efforts on disease control programs in this valuable aquaculture species.

摘要

为了增强基因组资源并了解病原体反应的分子免疫机制,我们首先通过 RNA-Seq 技术对微球菌溶壁酶免疫的卤虫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)。总共获得了 80、113、984 条清洁读数,然后组装成 71536 条 unigenes,平均长度为 1115 bp,N50 为 1783 bp。通过与 nr、Swiss-Prot\KEGG\COG\KOG\GO 和 Pfam 数据库进行比对,对 unigenes 进行了注释,27689 条 unigenes(38.7%)在至少一个数据库中得到注释。在细菌攻毒后,分别有 183 个和 298 个基因被鉴定为显著上调或下调,其中 481 个基因与 168 条途径相关,包括经典的免疫相关途径,如“Toll-like receptor signaling”、“the complement cascades”、“MAPK signaling pathway”和“Apoptosis”。此外,通过使用定量实时 PCR 验证了 8 个表达不同的免疫相关基因。本研究首次对正常和微球菌溶壁酶免疫的卤虫进行了基因表达模式描述,为进一步研究该有价值的水产养殖物种的疾病控制方案提供了新的思路。

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