叙利亚仓鼠和恒河猴的柯萨奇病毒 B3 手足口病动物模型。

IF 5.5 3区 医学 Q1 Medicine
Suqin Duan , Wei Zhang , Yongjie Li, Yanyan Li, Yuan Zhao, Weihua Jin, Quan Liu, Mingxue Li, Wenting Sun, Lixiong Chen, Hongjie Xu, Jie Tang, Jinghan Hou, Zijun Deng, Fengmei Yang, Shaohui Ma, Zhanlong He
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引用次数: 0

摘要

柯萨奇病毒 B3(CVB3)是引起手足口病(HFMD)的病原体,其临床表现从轻微到严重不等。然而,传统的 CVB3 感染小鼠研究主要导致病毒性心肌炎和胰腺炎,无法复制手足口病的症状。这限制了我们对 CVB3 病毒与宿主相互作用的了解。同时,不同临床表现的动物模型可有效加速 CVB3 新型疗法和疫苗的开发。叙利亚仓鼠和恒河猴已被广泛用于评估多种肠道病毒,但 CVB3 尚未被系统报道。在本研究中,我们首先检测了叙利亚仓鼠通过不同途径感染 CVB3 的易感性。我们的研究发现,腹腔注射和鼻腔滴注都能有效地使 CVB3 感染叙利亚仓鼠,导致其出现特征性手足口病症状、鼻咽部定植和急性严重病理损伤。值得注意的是,滴鼻组的排毒周期更长,病理损伤更严重。在随后的研究中,通过滴鼻感染 CVB3 的猕猴也出现了手足口病的症状、排毒、血清抗体转换、病毒核酸和抗原以及心脏等特定器官的病理损伤。令人惊讶的是,心肌酶水平没有发现明显差异。而且临床表现与常见的轻度感染相似。总之,该研究建立了CVB3重症叙利亚仓鼠和轻症恒河猴手足口病模型,为了解发病机制、试验前预防和评估以及暴露后干预奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coxsackievirus B3 HFMD animal models in Syrian hamster and rhesus monkey

Coxsackievirus B3 (CVB3) is the pathogen causing hand, foot and mouth disease (HFMD), which manifests across a spectrum of clinical severity from mild to severe. However, CVB3-infected mouse models mainly demonstrate viral myocarditis and pancreatitis, failing to replicate human HFMD symptoms. Although several enteroviruses have been evaluated in Syrian hamsters and rhesus monkeys, there is no comprehensive data on CVB3. In this study, we have first tested the susceptibility of Syrian hamsters to CVB3 infection via different routes. The results showed that Syrian hamsters were successfully infected with CVB3 by intraperitoneal injection or nasal drip, leading to nasopharyngeal colonization, acute severe pathological injury, and typical HFMD symptoms. Notably, the nasal drip group exhibited a longer viral excretion cycle and more severe pathological damage. In the subsequent study, rhesus monkeys infected with CVB3 through nasal drips also presented signs of HFMD symptoms, viral excretion, serum antibody conversion, viral nucleic acids and antigens, and the specific organ damages, particularly in the heart. Surprisingly, there were no significant differences in myocardial enzyme levels, and the clinical symptoms resembled those often associated with common, mild infections. In summary, the study successfully developed severe Syrian hamsters and mild rhesus monkey models for CVB3-induced HFMD. These models could serve as a basis for understanding the disease pathogenesis, conducting pre-trial prevention and evaluation, and implementing post-exposure intervention.

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来源期刊
Virologica Sinica
Virologica Sinica Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
7.70
自引率
1.80%
发文量
3149
期刊介绍: Virologica Sinica is an international journal which aims at presenting the cutting-edge research on viruses all over the world. The journal publishes peer-reviewed original research articles, reviews, and letters to the editor, to encompass the latest developments in all branches of virology, including research on animal, plant and microbe viruses. The journal welcomes articles on virus discovery and characterization, viral epidemiology, viral pathogenesis, virus-host interaction, vaccine development, antiviral agents and therapies, and virus related bio-techniques. Virologica Sinica, the official journal of Chinese Society for Microbiology, will serve as a platform for the communication and exchange of academic information and ideas in an international context. Electronic ISSN: 1995-820X; Print ISSN: 1674-0769
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