解剖鳜鱼幽门盲肠对急性ranv (MRV)感染的整体反应揭示了浆液炎的形成,然后是腹水。

IF 4 2区 医学 Q2 VIROLOGY
Wenfeng Zhang, Yong Li, Xiaosi Wu, Qianqian Sun, Yuting Fu, Shaoping Weng, Jianguo He, Chuanfu Dong
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引用次数: 0

摘要

鳜鱼拉纳病毒(MRV)是虹膜病毒科拉纳病毒属的一个新成员,与著名的大口黑鲈病毒(LMBV)具有98%以上的全基因组同源性。我们最近的工作表明,急性MRV感染主要影响幽门盲肠,这是鳜鱼的一个重要内脏器官,并被假设驱动严重腹水的特征性外部临床症状。在这项研究中,我们发现急性MRV感染最初以鳜鱼幽门盲肠的浆膜层为靶点,导致迅速发展为纤维性浆膜炎,其特征是浆膜肥大、纤维化、充血、水肿和组织粘连。利用单细胞RNA测序,研究人员分析了上皮细胞、免疫细胞和基质细胞的细胞组成,发现巨噬细胞和粒细胞的显著富集,以及T细胞和自然杀伤细胞,是急性细胞因子和炎症反应的关键介质。然后,强有力的实验证据表明,MRV感染特定的免疫细胞亚群T和B细胞以及成纤维细胞、肌成纤维细胞、内皮细胞和周细胞的基质细胞,导致增生性浆膜带中与细胞外基质(ECM)形成、胶原生物合成和血管重塑相关的基因和通路上调。此外,宿主衍生的V型胶原和mrv编码的胶原都与增生性浆膜中的ECM形成有关。总的来说,本研究提供了幽门盲肠对急性MRV感染反应的全面单细胞分辨率分析,并强调病毒驱动的浆膜炎是鳜鱼严重腹水的潜在原因。幽门盲肠是许多硬骨鱼类的重要消化和免疫器官,包括鳜鱼,一种肉食性鱼类,其幽门盲肠异常发达,每个人有207-326个盲肠。虽然MRV/LMBV感染多种鱼类,但严重腹水仅在受感染的鳜鱼中观察到。本研究表明,急性MRV感染可诱发幽门盲肠纤维性浆液炎,以充血、水肿和增生为特征,最终导致腹水和死亡。利用单细胞RNA测序,我们提供了受炎症反应影响或参与炎症反应的细胞类型的详细图景,揭示了它们在血清炎发病机制中的作用。这些发现促进了我们对mrv诱导的病理及其物种特异性表现的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dissection of the global responses of mandarin fish pyloric cecum to an acute ranavirus (MRV) infection reveals the formation of serositis and then ascites.

Mandarin fish ranavirus (MRV), a new member of the species Ranavirus micropterus1, sharing over 98% whole-genome nucleotide identity with the well-known largemouth bass virus (LMBV), is a distinct member of the genus Ranavirus within the family Iridoviridae. Our recent work showed that acute MRV infection predominantly affects the pyloric cecum, a critical visceral organ in mandarin fish, and was hypothesized to drive the characteristic external clinical sign of severe ascites. In this study, we reveal that acute MRV infection initially targets the serosal layer of the pyloric cecum of mandarin fish, leading to rapid progression into fibrinous serositis characterized by serosal hypertrophy, fibrosis, hyperemia, edema, and tissue adhesions. Using single-cell RNA sequencing, we dissect the cellular composition of epithelial, immune, and stromal populations, identifying significant enrichment of macrophages and granulocytes, alongside T and natural killer cells, as key mediators of acute cytokine and inflammatory responses. Then, robust experimental evidence demonstrates that MRV infects specific immune cell subsets of T and B cells and stromal cells of fibroblasts, myofibroblasts, endothelial cells, and pericytes, resulting in upregulation of genes and pathways associated with extracellular matrix (ECM) formation, collagen biosynthesis, and vascular remodeling in the hyperplastic serosal zone. Additionally, both host-derived type V collagens and MRV-encoded collagens are implicated in ECM formation in the hypertrophic serosa. Collectively, this study provides a comprehensive single-cell resolution analysis of the pyloric cecum's response to acute MRV infection and highlights virus-driven serositis as the underlying cause of severe ascites in mandarin fish.IMPORTANCEThe pyloric cecum is a vital digestive and immune organ in many bony fish species, including the mandarin fish, a carnivorous species with an exceptionally developed pyloric cecum comprising 207-326 ceca per individual. While MRV/LMBV infects various fish species, severe ascites is uniquely observed in infected mandarin fish. This study demonstrates that acute MRV infection induces fibrinous serositis in the pyloric cecum, characterized by hyperemia, edema, and hyperplasia, ultimately resulting in ascites and mortality. Leveraging single-cell RNA sequencing, we provide a detailed landscape of the cell types affected or involved in the inflammatory response, revealing their roles in the pathogenesis of serositis. These findings advance our understanding of MRV-induced pathology and its species-specific manifestations.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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