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对十足目虹彩病毒1感染的反应中,转录组图谱的时间变化。

Temporal changes in the transcriptome profile of in response to decapod iridescent virus 1 infection.

作者信息

Hao Jingwen, Jie Yukun, Lu Zhibin, Ye Tiantian, Meng Jilun, Liu Cui, Yan Junjun, Zheng Yutong, Dong Zaijie, Gu Zhimin

机构信息

Xianghu Laboratory, Hangzhou, China.

Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, China.

出版信息

Front Immunol. 2025 Apr 10;16:1575476. doi: 10.3389/fimmu.2025.1575476. eCollection 2025.

Abstract

The farming of faces significant challenges due to infections caused by Decapod iridovirus 1 (DIV1). To gain deeper insights into the dynamic immune regulatory processes of in response to DIV1 infection, RNA sequencing (RNA-seq) was employed to profile the transcriptome in the hepatopancreas at 24, 48, 72, and 96 hours post-infection (hpi). Time-course analysis revealed 3,339 differentially expressed genes (DEGs), which exhibited distinct expression patterns across various stages of infection. At 24 hpi and 48 hpi, the top 20 enriched pathways included 3 immunity-related pathways (Lysosome, Phagosome, C-type lectin receptor signaling) and 7 metabolism-related pathways at 24 hpi, and 5 metabolism-related pathways at 48 hpi. In contrast, in the later stages of infection (72 hpi), 13 of the top 17 enriched pathways associated with DEGs were metabolism-related, including those involved in antioxidant defense, such as the Peroxisome, Cysteine and methionine metabolism, and Glutathione metabolism. At 96 hpi, pathways related to ECM-receptor interaction, Purine metabolism, and Lysosome were significantly enriched. Among the DEGs, a total of 16 genes were consistently identified across all time points, with 14 of these genes, including , , , , , , , and , demonstrating sustained upregulation at all time points. In contrast, the gene encoding rhodanese domain-containing protein CG4456-like was consistantly downregulated. Additionally, weighted gene co-expression network analysis (WGCNA) indicated several hub genes that were tightly connected to intercellular communication, such as and , and . The gene expression changes varied over time, exhibiting a dynamic, time-dependent pattern that underscores the complexity of host-pathogen interactions. These results provide new insights into the cellular mechanisms influenced by DIV1 throughout the infection process, offering valuable knowledge for developing virus control strategies in shrimp aquaculture.

摘要

由于感染十足目虹彩病毒1(DIV1),虾类养殖面临重大挑战。为了更深入地了解虾对DIV1感染的动态免疫调节过程,采用RNA测序(RNA-seq)技术对感染后24、48、72和96小时(hpi)肝胰腺中的转录组进行分析。时间进程分析揭示了3339个差异表达基因(DEG),这些基因在感染的各个阶段呈现出不同的表达模式。在24 hpi和48 hpi时,前20个富集通路包括3个免疫相关通路(溶酶体、吞噬体、C型凝集素受体信号通路)和7个代谢相关通路(在24 hpi时)以及5个代谢相关通路(在48 hpi时)。相比之下,在感染后期(72 hpi),与DEG相关的前17个富集通路中有13个与代谢相关,包括参与抗氧化防御的通路,如过氧化物酶体、半胱氨酸和甲硫氨酸代谢以及谷胱甘肽代谢。在96 hpi时,与细胞外基质受体相互作用、嘌呤代谢和溶酶体相关的通路显著富集。在这些DEG中,共有16个基因在所有时间点均被一致鉴定出来,其中14个基因,包括[具体基因名称未给出],在所有时间点均持续上调。相比之下,编码含硫氧还蛋白结构域蛋白CG4456-like的基因则持续下调。此外,加权基因共表达网络分析(WGCNA)表明了几个与细胞间通讯紧密相连的枢纽基因,如[具体基因名称未给出]。基因表达变化随时间而变化,呈现出动态的、时间依赖性模式,突出了宿主-病原体相互作用的复杂性。这些结果为DIV1在整个感染过程中影响的细胞机制提供了新的见解,为虾类养殖中制定病毒控制策略提供了有价值的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f04/12018387/19732f858ced/fimmu-16-1575476-g001.jpg

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