Unraveling the innate immune responses of Bombyx mori hemolymph, fat body, and midgut to Bombyx mori nucleopolyhedrovirus oral infection by metabolomic analysis

家蚕 生物 血淋巴 中肠 代谢组学 家蚕 代谢途径 先天免疫系统 小桶 生物化学 脂肪酸代谢 微生物学 新陈代谢 基因 转录组 基因表达 植物 生物信息学 受体 幼虫
作者
Guobao Wang,Dandan Xu,Dingge Guo,Yuzhuo Zhang,Xiaoxi Mai,Zhang Baoren,Hui Cao,Shengxiang Zhang
出处
期刊:Archives of Insect Biochemistry and Physiology [Wiley]
卷期号:108 (4) 被引量:6
标识
DOI:10.1002/arch.21848
摘要

Abstract Bombyx mori nucleopolyhedrovirus (BmNPV) infection causes a series of physiological and pathological changes in Bombyx mori ( B. mori ). Here, a metabolomic study of the innate immunity organs including hemolymph, fat body, and midgut of the silkworm strain Dazao following BmNPV challenge was conducted to reveal the metabolic variations in B. mori . Compared to the control, 4964 and 4942 features with 4077 and 4327 high‐quality features were generated under positive and negative modes, respectively, from BmNPV‐infected larvae. The principal component analysis and supervised learning method using partial least squares discrimination analysis demonstrated good analytical stability and experimental reproducibility of the metabolic profiles. Based on database annotations, a total of 296, 108, and 215 differential expressed metabolites (DEMs) were identified from BmNPV‐infected group of hemolymph, fat body, and midgut, respectively, which were all mainly grouped into carboxylic acids and derivatives, fatty acyls, and glycerophospholipids. Kyoto Encyclopedia of Genes and Genomes Database enrichment analysis of the DEMs showed that amino acid metabolism was increased at 24 h after BmNPV infection. BmNPV induction was adopted to significantly alter a series of immune‐related pathways including phospholipase D signaling pathway, FoxO signaling pathway, metabolism of xenobiotics by cytochrome P450, melanogenesis, membrane transport, carbohydrate metabolism, and lipid metabolism. The different levels of expression of several DEMs including l ‐glutamate, naphthalene, 3‐succinoylpyridine 1‐acyl‐sn‐glycerol 3‐phosphate, and l ‐tyrosine which were involved in those pathways exhibited the immune responses of B. mori to BmNPV infection. Our findings are valuable for a better understanding of the antiviral mechanism of B. mori underlying the interaction between the silkworm and BmNPV.
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