Identification and comparative analysis of the Eriocheir sinensis microRNA transcriptome response to Spiroplasma eriocheiris infection using a deep sequencing approach

被引:68
|
作者
Ou, Jiangtao [1 ,2 ]
Meng, Qingguo [1 ,2 ]
Li, Yue [1 ,2 ]
Xiu, Yunji [1 ,2 ]
Du, Jie [1 ,2 ]
Gu, Wei [1 ,2 ]
Wu, Ting [1 ,2 ]
Li, Wenjie [1 ,2 ]
Ding, Zhengfeng [1 ,2 ]
Wang, Wen [1 ,2 ]
机构
[1] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Biodivers & Biotechnol, Nanjing 210046, Jiangsu, Peoples R China
[2] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Aquat Crustacean Dis, Nanjing 210046, Jiangsu, Peoples R China
关键词
Eriocheir sinensis; Spiroplasma eriocheiris; Next generation sequencing; Immune-related microRNAs; Host-pathogen interaction; CHINESE MITTEN CRAB; RNA CDNA LIBRARIES; IMMUNE-RELATED GENES; INNATE IMMUNITY; CELL PROLIFERATION; TREMOR DISEASE; EXPRESSION; CONSTRUCTION; HEMOCYTES; EVOLUTION;
D O I
10.1016/j.fsi.2011.11.027
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The Chinese mitten crab Eriocheir sinensis is one of the most important freshwater aquaculture crustacean species in China. MicroRNAs (miRNAs) are small non-coding RNAs that are important effectors in the intricate host pathogen interaction network. To increase the repertoire of miRNAs characterized in crustaceans and to examine the relationship between host miRNA expression and pathogen infection, we used the Illumina/Solexa deep sequencing technology to sequence two small RNA libraries prepared from haemocytes of E. sinensis under normal conditions and during infection with Spiroplasma eriocheiris. The high-throughput sequencing resulted in approximately 30,975,151 and 30,826,277 raw reads corresponding to 12,077,088 and 16,271,545 high-quality mappable reads for the normal and infected haemocyte samples, respectively. Bioinformatic analyses identified 735 unique miRNAs, including 36 that are conserved in crustaceans, 134 that are novel to crabs but are present in other arthropods (PN-type), and 565 that are completely new (PC-type). Two hundred twenty-eight unique miRNAs displayed significant differential expression between the normal and infected haemocyte samples (p < 0.0001). Of these, 133 (58%) were significantly up-regulated and 95 (42%) were significantly down-regulated upon challenge with S. eriocheiris. Real-time quantitative PCR (RT-qPCR) experiments were preformed for 10 miRNAs of the two samples, and agreement was found between the sequencing and RT-qPCR data. To our knowledge, this is the first report of comprehensive identification of E. sinensis miRNAs and of expression analysis of E. sinensis miRNAs after exposure to S. eriocheiris. Many miRNAs were differentially regulated when exposed to the pathogen, and these findings support the hypothesis that certain miRNAs might be essential in host pathogen interactions. Our results suggest that elucidation of the molecular mechanisms responsible for miRNA regulation of the host's innate immune system should help with the development of new control strategies to prevent or treat S. eriocheiris infections in crustaceans. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:345 / 352
页数:8
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