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Transcriptome Analysis of the Midgut of the Chinese Oak Silkworm Antheraea pernyi Infected with Antheraea pernyi Nucleopolyhedrovirus

机译:Oak蚕An蚕核多角体病毒感染中国Oak蚕中肠的转录组分析

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摘要

The Antheraea pernyi nucleopolyhedrovirus (ApNPV) is an exclusive pathogen of A. pernyi. The intense interactions between ApNPV and A. pernyi cause a series of physiological and pathological changes to A. pernyi. However, no detailed report exists regarding the molecular mechanisms underlying the interactions between ApNPV and A. pernyi. In this study, four cDNA libraries of the A. pernyi midgut, including two ApNPV-infected groups and two control groups, were constructed for transcriptomic analysis to provide new clues regarding the molecular mechanisms that underlie these interactions. The transcriptome of the A. pernyi midgut was de novo assembled using the Trinity platform because of the lack of a genome resource for A. pernyi. Compared with the controls, a total of 5,172 differentially expressed genes (DEGs) were identified, including 2,183 up-regulated and 2,989 down-regulated candidates, of which 2,965 and 911 DEGs were classified into different GO categories and KEGG pathways, respectively. The DEGs involved in A. pernyi innate immunity were classified into several categories, including heat-shock proteins, apoptosis-related proteins, serpins, serine proteases and cytochrome P450s. Our results suggested that these genes were related to the immune response of the A. pernyi midgut to ApNPV infection via their essential roles in regulating a variety of physiological processes. Our results may serve as a basis for future research not only on the molecular mechanisms of ApNPV invasion but also on the anti-ApNPV mechanism of A. pernyi.
机译:多年生花丝虫核多角体病毒(ApNPV)是多年生曲霉的唯一病原体。 ApNPV与A. pernyi之间的强烈相互作用导致A. pernyi发生一系列生理和病理变化。但是,关于ApNPV和A. pernyi之间相互作用的分子机制,尚无详细报道。在这项研究中,构建了pernyi中肠的四个cDNA文库,包括两个被ApNPV感染的组和两个对照组,用于转录组学分析,以提供有关这些相互作用基础的分子机制的新线索。由于缺少A. pernyi的基因组资源,使用Trinity平台从头组装了A. pernyi中肠的转录组。与对照组相比,共鉴定了5,172个差异表达基因(DEG),包括2,183个上调候选基因和2,989个下调候选基因,其中2,965个和911个DEG分别分类为不同的GO类别和KEGG途径。参与peremi 先天免疫的DEGs分为几类,包括热激蛋白,凋亡相关蛋白,丝氨酸蛋白酶抑制剂,丝氨酸蛋白酶和细胞色素P450。我们的结果表明,这些基因与 A 的免疫反应有关。 pernyi 中肠通过其在调节各种生理过程中的重要作用而感染ApNPV。我们的研究结果不仅可以作为ApNPV入侵的分子机制,而且可以作为 A 的抗ApNPV机制的基础。 pernyi

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