College of Life Sciences, Henan Agricultural University, Zhengzhou 450002, China.
College of Plant Protection, Henan Agricultural University, Zhengzhou 450002, China.
Viruses. 2022 Dec 21;15(1):19. doi: 10.3390/v15010019.
MicroRNAs (miRNAs), are a novel class of gene expression regulators, that have been found to participate in regulating host-virus interactions. However, the function of insect-derived miRNAs in response to virus infection is poorly understood. We analyzed miRNA expression profiles in the fat bodies of () infected with multiple nucleopolyhedroviruses (MbMNPV). A total of 52 differentially expressed miRNAs (DEmiRNAs) were filtered out through RNA-seq analysis. The targets of 52 DEmiRNAs were predicted and 100 miRNA-mRNA interaction pairs were obtained. The predicted targets of DEmiRNAs were mainly enriched in the Wnt signaling pathway, phagosome, and mTOR signaling pathway, which are related to the virus infection. Real-time PCR was used to verify the RNA sequencing results. ame-miR-317-3p, mse-miR-34, novel1-star, and sfr-miR-6094-5p were shown to be involved in the host response to MbMNPV infection. Results suggest that sfr-miR-6094-5p can negatively regulate the expression of four host genes eIF3-S7, CG7583, CG16901, and btf314, and inhibited MbMNPV infection significantly. Further studies showed that RNAi-mediated knockdown of eIF3-S7 inhibited the MbMNPV infection. These findings suggest that sfr-miR-6094-5p inhibits MbMNPV infection by negatively regulating the expression of eIF3-S7. This study provides new insights into MbMNPV and interaction mechanisms.
微小 RNA(miRNAs)是一类新的基因表达调控因子,已发现它们参与宿主-病毒相互作用的调节。然而,昆虫衍生的 miRNAs 对病毒感染的反应功能知之甚少。我们分析了感染 ()的脂肪体中的 miRNA 表达谱 多种核多角体病毒(MbMNPV)。通过 RNA-seq 分析筛选出 52 个差异表达的 miRNAs(DEmiRNAs)。预测了 52 个 DEmiRNAs 的靶标,并获得了 100 个 miRNA-mRNA 相互作用对。DEmiRNAs 的预测靶标主要富集在 Wnt 信号通路、吞噬体和 mTOR 信号通路,这些通路与病毒感染有关。实时 PCR 用于验证 RNA 测序结果。ame-miR-317-3p、mse-miR-34、novel1-star 和 sfr-miR-6094-5p 被证明参与宿主对 MbMNPV 感染的反应。结果表明,sfr-miR-6094-5p 可以负调控 eIF3-S7、CG7583、CG16901 和 btf314 四个宿主基因的表达,并显著抑制 MbMNPV 感染。进一步的研究表明,RNAi 介导的 eIF3-S7 敲低抑制了 MbMNPV 感染。这些发现表明,sfr-miR-6094-5p 通过负调控 eIF3-S7 的表达抑制 MbMNPV 感染。本研究为 MbMNPV 和 相互作用机制提供了新的见解。