Xing Shanshan, Du Junzheng, Gao Shandian, Tian Zhancheng, Zheng Yadong, Liu Guangyuan, Luo Jianxun, Yin Hong
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Lanzhou, Gansu 730046, PR China.
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Lanzhou, Gansu 730046, PR China.
Infect Genet Evol. 2016 Apr;39:74-84. doi: 10.1016/j.meegid.2016.01.012. Epub 2016 Jan 13.
Cellular microRNAs (miRNAs) have been reported to be key regulators of virus-host interactions. Bluetongue virus (BTV) is an insect-borne virus that causes huge economic losses in the livestock industry worldwide. Aedes albopictus cell lines have become powerful and convenient tools for studying BTV-vector interactions. However, the role of miRNAs in A. albopictus cells during BTV infection is not well understood. In this study, we performed a deep sequencing analysis of small RNA libraries of BTV-infected and mock-infected A. albopictus cells, and a total of 11,206,854 and 12,125,274 clean reads were identified, respectively. A differential expression analysis showed that 140 miRNAs, including 15 known and 125 novel miRNAs, were significantly dysregulated after infection, and a total of 414 and 2307 target genes were annotated, respectively. Real-time quantitative reverse transcription-polymerase chain reaction validated the expression patterns of 11 selected miRNAs and their mRNA targets. Functional annotation of the target genes suggested that these target genes were mainly involved in metabolic pathways, oxidative phosphorylation, endocytosis, RNA transport, as well as the FoxO, Hippo, Jak-STAT, and MAPK signaling pathways. This is the first systematic study on the effect of BTV infection on miRNA expression in A. albopictus cells. This investigation provides information concerning the cellular miRNA expression profile in response to BTV infection, and it offers clues for identifying potential candidates for vector-based antiviral strategies.
据报道,细胞微小RNA(miRNA)是病毒与宿主相互作用的关键调节因子。蓝舌病毒(BTV)是一种虫媒病毒,在全球畜牧业中造成巨大经济损失。白纹伊蚊细胞系已成为研究BTV与载体相互作用的强大而便捷的工具。然而,miRNA在BTV感染期间白纹伊蚊细胞中的作用尚不清楚。在本研究中,我们对BTV感染和模拟感染的白纹伊蚊细胞的小RNA文库进行了深度测序分析,分别鉴定出11,206,854和12,125,274条clean reads。差异表达分析表明,140种miRNA,包括15种已知miRNA和125种新miRNA,在感染后显著失调,分别注释了414个和2307个靶基因。实时定量逆转录-聚合酶链反应验证了11种选定miRNA及其mRNA靶标的表达模式。靶基因的功能注释表明,这些靶基因主要参与代谢途径、氧化磷酸化、内吞作用、RNA转运,以及FoxO、Hippo、Jak-STAT和MAPK信号通路。这是首次关于BTV感染对白纹伊蚊细胞中miRNA表达影响的系统研究。本研究提供了关于细胞miRNA表达谱对BTV感染反应的信息,并为鉴定基于载体的抗病毒策略的潜在候选物提供了线索。