College of Bioscience and Biotechnology, Liaoning Engineering & Technology Research Center for Insect Resources, Shenyang Agricultural University, Shenyang 110866, China.
College of Bioscience and Biotechnology, Liaoning Engineering & Technology Research Center for Insect Resources, Shenyang Agricultural University, Shenyang 110866, China.
J Invertebr Pathol. 2019 Sep;166:107205. doi: 10.1016/j.jip.2019.107205. Epub 2019 May 25.
Insects have evolved efficient innate immune systems to defend themselves against the invasion of pathogens and parasites. We infected the lepidopteran Antheraea pernyi with Antheraea pernyi nucleopolyhedrovirus (ApNPV) and studied the host's transcriptional response to unravel the cellular and humoral immune responses of A. pernyi larval hemolymph to ApNPV. Comparison of gene expression levels revealed that a total of 3191 genes were differentially expressed, including 1107 up-regulated and 2084 down-regulated genes in ApNPV-infected hemolymph. Of these, 1416 and 982 differentially expressed genes (DEGs) were enriched in 3253 Gene Ontology terms and 258 KEGG pathways, respectively. DEGs involved in immunity related pathways were selected for further analysis. We screened 184 and 63 DEGs involved in cellular and humoral immune-related pathways, respectively, via KEGG analysis. Among the cellular immune-related pathways, autophagy, endocytosis, and lysosome were activated based on the expression profiles of several key regulatory genes, such as the up-regulation of Atg3 and LPS-induced TN factor, and the down-regulation of PIK3R4, HSC70 and V-ATPase. We concluded that phagosome, apoptosis, and ubiquitin-mediated proteolysis were suppressed by ApNPV as a result of down-regulation of most related DEGs. The majority of the DEGs enriched in Toll, Jak-STAT, MAPK, NF-κB and Insulin signaling pathways, complement and coagulation cascades, and melanogenesis were down-regulated, demonstrating that ApNPV infection greatly inhibited humoral immunity in the hemolymph of A. pernyi larvae. Our findings may serve as a basis for further research on the antiviral molecular mechanisms of A. pernyi.
昆虫已经进化出高效的先天免疫系统来抵御病原体和寄生虫的入侵。我们用野蚕核型多角体病毒(ApNPV)感染鳞翅目昆虫野蚕,并研究了宿主的转录反应,以揭示野蚕幼虫血淋巴中的细胞和体液免疫反应。比较基因表达水平表明,共有 3191 个基因差异表达,其中 ApNPV 感染血淋巴中 1107 个上调和 2084 个下调基因。其中,1416 和 982 个差异表达基因(DEGs)分别在 3253 个基因本体论术语和 258 个 KEGG 途径中富集。DEGs 参与免疫相关途径的分析。通过 KEGG 分析,我们筛选了 184 个和 63 个分别与细胞和体液免疫相关途径相关的 DEGs。在细胞免疫相关途径中,根据几个关键调节基因的表达谱,如 Atg3 和 LPS 诱导的 TN 因子的上调以及 PIK3R4、HSC70 和 V-ATPase 的下调,激活了自噬、内吞作用和溶酶体。我们得出结论,由于大多数相关 DEGs 的下调,吞噬体、凋亡和泛素介导的蛋白水解被 ApNPV 抑制。在 Toll、Jak-STAT、MAPK、NF-κB 和胰岛素信号通路、补体和凝血级联以及黑色素生成中富集的大多数 DEGs 下调,表明 ApNPV 感染极大地抑制了野蚕幼虫血淋巴中的体液免疫。我们的发现可以为进一步研究野蚕的抗病毒分子机制提供基础。