School of Marine Sciences, Sun Yat-sen University, Guangzhou, China.
Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), Zhuhai, China.
J Fish Dis. 2021 Sep;44(9):1305-1314. doi: 10.1111/jfd.13389. Epub 2021 May 28.
Nervous necrosis virus (NNV) is one of the most destructive fish viruses and affects more than 120 marine and freshwater teleost species. However, the pathogenesis of NNV has not been made clear. MicroRNAs (miRNAs) play important roles in the regulation of viral infection. To understand the roles and regulation patterns of miRNAs in NNV infection, high-throughput sequencing was carried out in Lateolabrax japonicus brain (LJB) cells with or without red-spotted grouper NNV (RGNNV) infection at 12 and 24 hr. Here, we identified 59 known and 61 novel differentially expressed miRNAs (DE miRNAs) between mock and RGNNV-infected LJB cells. KEGG pathway analysis showed that the target genes of DE miRNAs were significantly enriched in immune-related signalling pathways, such as autophagy, mitophagy and TGF-beta signalling pathways. The expression patterns of four DE miRNAs (lja-miR-145, lja-miR-182, lja-miR-183 and lja-miR-187) were verified by qRT-PCR both in vivo and in vitro. We found that lja-miR-145 promoted RGNNV proliferation, while lja-miR-183 suppressed RGNNV proliferation. Furthermore, lja-miR-145 facilitated RGNNV-induced autophagy activation, whereas lja-miR-183 repressed autophagy in LJB cells as measured by LC3B-II/I and p62 protein levels. All these results indicate the involvement of lja-miR-145 and lja-miR-183 in RGNNV-induced autophagy. In conclusion, this study provides evidence for the important roles of miRNAs in NNV infection and a basis for uncovering the molecular regulation mechanism of NNV-induced autophagy.
神经坏死病毒(NNV)是一种极具破坏性的鱼类病毒,可感染 120 多种海洋和淡水硬骨鱼类。然而,NNV 的发病机制尚未阐明。microRNAs(miRNAs)在病毒感染的调控中发挥着重要作用。为了了解 miRNAs 在 NNV 感染中的作用和调控模式,本研究在红鳍东方鲀脑(LJB)细胞中进行了高通量测序,这些细胞在感染 NNV 前后 12 和 24 小时分别进行了 mock 和 RGNNV 感染。在此,我们在 mock 和 RGNNV 感染的 LJB 细胞之间鉴定了 59 个已知和 61 个新的差异表达 miRNA(DE miRNAs)。KEGG 通路分析表明,DE miRNAs 的靶基因显著富集在免疫相关信号通路中,如自噬、线粒体自噬和 TGF-β信号通路。通过 qRT-PCR 分别在体内和体外验证了四个 DE miRNAs(lja-miR-145、lja-miR-182、lja-miR-183 和 lja-miR-187)的表达模式。研究发现,lja-miR-145 促进了 RGNNV 的增殖,而 lja-miR-183 则抑制了 RGNNV 的增殖。此外,lja-miR-145 促进了 RGNNV 诱导的自噬激活,而 lja-miR-183 则通过 LC3B-II/I 和 p62 蛋白水平抑制了 LJB 细胞中的自噬。所有这些结果表明,lja-miR-145 和 lja-miR-183 参与了 RGNNV 诱导的自噬。综上所述,本研究为 miRNAs 在 NNV 感染中的重要作用提供了证据,并为揭示 NNV 诱导自噬的分子调控机制奠定了基础。