基于气相色谱-质谱(GC-MS)的家蚕血淋巴代谢分析揭示了家蚕感染核多角体病毒后的四阶段代谢反应。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Molecular Biology Pub Date : 2024-10-31 DOI:10.1111/imb.12972
Zhenyue Su, Yi Li, Zihan Lin, Qing Huang, Xinyu Fan, Zhaoming Dong, Qingyou Xia, Ping Zhao, Xin Wang
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引用次数: 0

摘要

家蚕(Bombyx mori)是一种具有重要经济价值的昆虫,在丝绸生产中发挥着至关重要的作用。然而,家蚕育种极易受到各种病原体的感染,尤其是对家蚕构成严重威胁的蚕核多角体病毒(BmNPV)。最近的代谢组学研究揭示了与 BmNPV 感染相关的代谢变化。BmNPV 感染具有明显的时间特征。然而,很少有研究对不同时期感染的家蚕进行调查。本研究采用气相色谱-质谱联用技术(GC-MS)对家蚕感染后 48、72、96 和 120 h(h.p.i.)的血淋巴代谢物进行了全面分析。通过整合时间历程分析和京都基因组百科全书(KEGG)富集,该研究揭示了家蚕对 BmNPV 感染反应的四个阶段的代谢特征。在第一阶段(48 h.p.i.),家蚕激活抗氧化防御机制,涉及谷胱甘肽等关键抗氧化剂的代谢途径显著丰富,以减轻病毒入侵引起的氧化应激。到第二阶段(72 h.p.i.),与氨基酸代谢和蛋白质合成有关的途径开始活跃,表明蛋白质合成增加。在第 3 阶段(96 h.p.i.),能量代谢和物质运输途径显著上调,以支持病毒的快速复制和家蚕运动行为的增强。最后,在第 4 阶段(120 h.p.i.),与能量代谢、核酸合成和物质运输相关的途径进一步增强,这与病毒组装和释放的高峰期一致。这些发现有助于深入了解家蚕抗 NPV 的生化基础。
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GC-MS-based metabonomic analysis of silkworm haemolymph reveals four-stage metabolic responses to nucleopolyhedrovirus infection.

Silkworm, Bombyx mori, an economically significant insect, plays a crucial role in silk production. However, silkworm breeding is highly susceptible to various pathogens, particularly the Bombyx mori nucleopolyhedrovirus (BmNPV), which poses a serious threat. Recent metabonomic studies have provided insights into the metabolic changes associated with BmNPV infection. BmNPV infection has obvious temporal characteristics. However, few studies have investigated the silkworms infected in different periods. This study employed gas chromatography-mass spectrometry (GC-MS) to perform a comprehensive analysis of haemolymph metabolites in silkworms at 48, 72, 96 and 120 h post-infection (h.p.i.). Through the integration of time-course analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment, the study revealed distinct four-stage metabolic characteristics in the silkworm's response to BmNPV infection. At Stage 1 (48 h.p.i.), silkworms activate antioxidant defence mechanisms, with significant enrichment in metabolic pathways involving key antioxidants such as glutathione, to mitigate oxidative stress induced by viral invasion. By Stage 2 (72 h.p.i.), pathways related to amino acid metabolism and protein synthesis become active, indicating an increase in protein synthesis. In Stage 3 (96 h.p.i.), energy metabolism and substance transport pathways are significantly upregulated to support the rapid viral replication and the enhanced locomotor behaviour of silkworm. Finally, at Stage 4 (120 h.p.i.), there is a further enhancement of pathways related to energy metabolism, nucleic acid synthesis, and substance transport, which align with peak viral assembly and release. These findings contribute to an in-depth understanding of the biochemical basis of silkworm resistance to NPV.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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