Transcriptomic insights into the effects of Hepatospora eriocheir (Microsporidia) infection in Eriocheir sinensis

IF 3.7 2区 农林科学 Q1 FISHERIES
Fanya Nie , Xiao Zeng , Xing Lin , Jinyong Zhang , Yuanli Zhao
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Abstract

The Chinese mitten crab (Eriocheir sinensis), a key species in China’s freshwater aquaculture, faces growing threats from Hepatopancreatic Necrosis Syndrome caused by the microsporidian parasite Hepatospora eriocheir. Deciphering the molecular mechanisms underlying host-pathogen interactions is essential for developing effective disease control strategies. While alternative splicing (AS) and alternative polyadenylation (APA) represent a critical regulatory mechanism in immune responses to pathogenic challenges, their functional significance in E. sinensis remains poorly characterized. This study employed RNA-seq to analyze hepatopancreas transcriptomes during H. eriocheir infection, systematically investigating differentially expressed genes (DEGs), AS and APA events dynamics. We identified 831 DEGs (|log2FoldChange| 1 and p-value < 0.05) enriched in immune-related pathways including G protein-coupled receptor signaling and epithelial morphogenesis. Additionally, 83 AS events and 914 APA events were detected, demonstrating their coordinated regulatory roles in infection responses. Our analysis revealed APA as a novel post-transcriptional modulator of host immunity, providing critical insights into molecular defense mechanisms against microsporidian invasion. These findings advance understanding of RNA processing regulation in invertebrate innate immunity and establish a framework for targeted disease management in crustacean aquaculture.
中华绒螯蟹肝孢子虫(微孢子虫)感染的转录组学研究
中华绒螯蟹(Eriocheir sinensis)是我国淡水养殖的重要物种,其肝胰腺坏死综合征(hbs)的威胁日益严重。破译宿主-病原体相互作用的分子机制对于制定有效的疾病控制策略至关重要。虽然选择性剪接(AS)和选择性聚腺苷酸化(APA)是免疫应答致病性挑战的关键调控机制,但它们在中华按蚊中的功能意义尚不清楚。本研究采用RNA-seq方法分析毛绒螯蟹感染过程中肝胰腺转录组,系统研究差异表达基因(DEGs)、AS和APA事件动态。我们发现了831个DEGs (|log2FoldChange|≥1和p值<; 0.05),这些DEGs富集于免疫相关途径,包括G蛋白偶联受体信号传导和上皮形态发生。此外,检测到83个AS事件和914个APA事件,证明了它们在感染反应中的协调调节作用。我们的分析表明,APA是一种新的宿主免疫转录后调节剂,为研究微孢子虫入侵的分子防御机制提供了重要的见解。这些发现促进了对无脊椎动物先天免疫中RNA加工调控的理解,并为甲壳类水产养殖中的靶向疾病管理建立了框架。
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来源期刊
Aquaculture Reports
Aquaculture Reports Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
5.90
自引率
8.10%
发文量
469
审稿时长
77 days
期刊介绍: Aquaculture Reports will publish original research papers and reviews documenting outstanding science with a regional context and focus, answering the need for high quality information on novel species, systems and regions in emerging areas of aquaculture research and development, such as integrated multi-trophic aquaculture, urban aquaculture, ornamental, unfed aquaculture, offshore aquaculture and others. Papers having industry research as priority and encompassing product development research or current industry practice are encouraged.
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