家蚕幼虫中肠单核测序揭示了感染后期BmNPV在中肠的免疫逃逸策略。

IF 3.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Biochemistry and Molecular Biology Pub Date : 2023-11-25 DOI:10.1016/j.ibmb.2023.104043
Junming Xia , Shigang Fei , Yigui Huang , Wenxuan Lai , Yue Yu , Lingying Liang , Hailin Wu , Luc Swevers , Jingchen Sun , Min Feng
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引用次数: 0

摘要

中肠是抵御微生物入侵和增殖的重要屏障,也是杆状病毒自然入侵宿主时首先遇到的组织。然而,不同的中肠细胞类型如何促进免疫反应和清除或促进病毒感染的知识有限。本文采用单核RNA测序(snRNA seq)技术分析家蚕幼虫中肠不同细胞亚群对家蚕核型多角体病毒(BmNPV)感染的反应。在感染后72 h,我们在bmnpv感染和未感染的家蚕幼虫中肠中鉴定出22个不同的集群,分别代表肠内分泌细胞(EEs)、肠细胞(ECs)、肠干细胞(ISCs)、杯状细胞样细胞和肌肉细胞类型。此外,我们的研究结果表明,在感染后期,BmNPV在中肠的免疫逃逸策略包括:(1)抑制抗病毒途径的反应;(2)抑制抗病毒宿主因子的表达;(3)刺激BmNPV复制促进基因的表达水平。这些发现表明,中肠作为抵御杆状病毒侵袭的第一道防线,具有“抗性”和“耐受性”的双重特性。我们的单细胞数据集揭示了家蚕幼虫中肠细胞的多样性,转录组分析提供了在单细胞水平上了解宿主与病毒感染之间相互作用的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Single-nucleus sequencing of silkworm larval midgut reveals the immune escape strategy of BmNPV in the midgut during the late stage of infection

The midgut is an important barrier against microorganism invasion and proliferation, yet is the first tissue encountered when a baculovirus naturally invades the host. However, only limited knowledge is available how different midgut cell types contribute to the immune response and the clearance or promotion of viral infection. Here, single-nucleus RNA sequencing (snRNA seq) was employed to analyze the responses of various cell subpopulations in the silkworm larval midgut to B. mori nucleopolyhedrovirus (BmNPV) infection. We identified 22 distinct clusters representing enteroendocrine cells (EEs), enterocytes (ECs), intestinal stem cells (ISCs), Goblet cell-like and muscle cell types in the BmNPV-infected and uninfected silkworm larvae midgut at 72 h post infection. Further, our results revealed that the strategies for immune escape of BmNPV in the midgut at the late stage of infection include (1) inhibiting the response of antiviral pathways; (2) inhibiting the expression of antiviral host factors; (3) stimulating expression levels of genes promoting BmNPV replication. These findings suggest that the midgut, as the first line of defense against the invasion of the baculovirus, has dual characteristics of "resistance" and "tolerance". Our single-cell dataset reveals the diversity of silkworm larval midgut cells, and the transcriptome analysis provides insights into the interaction between host and virus infection at the single-cell level.

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来源期刊
CiteScore
7.40
自引率
5.30%
发文量
105
审稿时长
40 days
期刊介绍: This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.
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Identification of a gene promoter active in Lucilia sericata larval salivary glands using a rapid transient expression assay. In vivo RNAi screening identifies multiple deubiquitinases required for the maintenance of intestinal homeostasis in Drosophila. JAK and STAT5B mediate olfactory response of migratory locusts to their own volatiles. Functional redundancy of the three insulin receptors of cockroaches. Editorial Board
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