Novel murine model of human astrovirus infection reveals cardiovascular tropism.

IF 4 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2025-05-20 Epub Date: 2025-04-30 DOI:10.1128/jvi.00240-25
Macee C Owen, Yuefang Zhou, Holly Dudley, Taylor Feehley, Ashley Hahn, Christine C Yokoyama, Margaret L Axelrod, Chieh-Yu Lin, David Wang, Andrew B Janowski
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引用次数: 0

Abstract

Astroviruses are a common cause of gastrointestinal disease in humans and have been linked to fatal cases of encephalitis. A major barrier to the study of human-infecting astroviruses is the lack of an in vivo model as previous attempts failed to identify a host that supports viral replication. We describe a novel murine model of infection using astrovirus VA1/HMO-C (VA1), an astrovirus with high seroprevalence in humans. VA1 is cardiotropic, and viral RNA levels peak in the heart tissue 7 days post-inoculation in multiple different murine genetic backgrounds. Infectious VA1 particles could be recovered from heart tissue 3 and 5 days post-inoculation. Viral capsid was detected intracellularly in the heart tissue by immunostaining, and viral RNA was detected in cardiac myocytes, endocardium, and endothelial cells based on fluorescent in situ hybridization and confocal microscopy. Histologically, we identified inflammatory infiltrates consistent with myocarditis in some mice, with viral RNA colocalizing with the infiltrates. These foci contained CD3 +T cells and CD68 +macrophages. Viral RNA levels increased by >10 fold in the heart tissue or serum samples from Rag1 or Stat1 knockout mice, demonstrating the role of both adaptive and innate immunity in the response to VA1 infection. Based on the in vivo tropisms, we tested cardiac-derived primary cells and determined that VA1 can replicate in primary human cardiac endothelial cells, suggesting a novel cardiovascular tropism in human cells. This novel in vivo model of a human-infecting astrovirus enables further characterization of the host immune response and reveals a new cardiovascular tropism of astroviruses.

Importance: Astroviruses routinely cause infections in humans; however, few methods were available to study these viruses. Here, we describe the first animal system to study human-infecting astroviruses by using mice. We demonstrate that mice are susceptible to astrovirus VA1, a strain that commonly infects humans and has been linked to fatal brain infections. The virus infects the heart tissue and is associated with inflammation. When mice with impaired immune systems were infected with VA1, they were found to have higher amounts of the virus in their hearts and blood. We found that VA1 can infect cells from human blood vessels of the heart, which is associated with human health. This model will enable us to better understand how astroviruses cause disease and how the immune system responds to infection. Our findings also suggest that astroviruses could be linked to cardiovascular diseases, including in humans.

人类星状病毒感染的新小鼠模型揭示心血管趋向性 。
星状病毒是人类胃肠道疾病的常见病因,并与脑炎的致命病例有关。研究人类感染的星状病毒的一个主要障碍是缺乏体内模型,因为以前的尝试未能确定支持病毒复制的宿主。我们描述了一种新的小鼠感染星状病毒VA1/HMO-C (VA1)模型,这是一种在人类中具有高血清阳性率的星状病毒。在多种不同遗传背景的小鼠中,VA1是嗜心性的,病毒RNA水平在接种后7天在心脏组织中达到峰值。接种后3和5 d可从心脏组织中回收感染性VA1颗粒。采用免疫染色法检测心脏组织细胞内的病毒衣壳,采用荧光原位杂交和共聚焦显微镜检测心肌细胞、心内膜和内皮细胞中的病毒RNA。组织学上,我们在一些小鼠中发现了与心肌炎一致的炎症浸润,病毒RNA与浸润共定位。这些病灶含有CD3 +T细胞和CD68 +巨噬细胞。在Rag1或Stat1敲除小鼠的心脏组织或血清样本中,病毒RNA水平增加了10倍,表明适应性免疫和先天免疫在对VA1感染的应答中都起作用。基于体内趋向性,我们测试了心脏来源的原代细胞,并确定VA1可以在原代人心脏内皮细胞中复制,这表明人类细胞中存在一种新的心血管趋向性。这种新的人类感染星状病毒的体内模型能够进一步表征宿主免疫反应,并揭示星状病毒的新心血管倾向。重要性:星状病毒通常会引起人类感染;然而,研究这些病毒的方法很少。在这里,我们描述了第一个用小鼠研究人类感染的星状病毒的动物系统。我们证明小鼠易感染星状病毒VA1,这是一种通常感染人类的毒株,与致命的脑部感染有关。这种病毒感染心脏组织,并与炎症有关。研究发现,当免疫系统受损的老鼠感染了VA1病毒后,它们的心脏和血液中病毒的含量更高。我们发现VA1可以感染来自人类心脏血管的细胞,这与人类健康有关。这个模型将使我们能够更好地了解星状病毒是如何引起疾病的,以及免疫系统是如何对感染作出反应的。我们的发现还表明,天体病毒可能与心血管疾病有关,包括人类的心血管疾病。
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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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