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不同小鼠品系、Wistar 大鼠和家兔实验性戊型肝炎病毒感染的不同结局。

Different Outcomes of Experimental Hepatitis E Virus Infection in Diverse Mouse Strains, Wistar Rats, and Rabbits.

机构信息

Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, 17493 Greifswald-Insel Riems, Germany.

Department of Experimental Animal Facilities and Biorisk Management, Friedrich-Loeffler-Institut, Südufer 10, 17493 Greifswald-Insel Riems, Germany.

出版信息

Viruses. 2018 Dec 20;11(1):1. doi: 10.3390/v11010001.

Abstract

Hepatitis E virus (HEV) is the causative agent of acute hepatitis E in humans in developing countries, but autochthonous cases of zoonotic genotype 3 (HEV-3) infection also occur in industrialized countries. In contrast to swine, rats, and rabbits, natural HEV infections in mice have not yet been demonstrated. The pig represents a well-established large animal model for HEV-3 infection, but a suitable small animal model mimicking natural HEV-3 infection is currently missing. Therefore, we experimentally inoculated C57BL/6 mice (wild-type, IFNAR, CD4, CD8) and BALB/c nude (nu/nu) mice, Wistar rats, and European rabbits with a wild boar-derived HEV-3 strain and monitored virus replication and shedding, as well as humoral immune responses. HEV RNA and anti-HEV antibodies were detected in one and two out of eight of the rats and all rabbits inoculated, respectively, but not in any of the mouse strains tested. Remarkably, immunosuppressive dexamethasone treatment of rats did not enhance their susceptibility to HEV infection. In rabbits, immunization with recombinant HEV-3 and ratHEV capsid proteins induced protection against HEV-3 challenge. In conclusion, the rabbit model for HEV-3 infection may serve as a suitable alternative to the non-human primate and swine models, and as an appropriate basis for vaccine evaluation studies.

摘要

戊型肝炎病毒 (HEV) 是发展中国家人类急性戊型肝炎的病原体,但在工业化国家也存在动物源性基因型 3 (HEV-3) 的感染。与猪、大鼠和兔子不同,自然感染 HEV 的小鼠尚未被证实。猪是一种已被充分证实的 HEV-3 感染的大型动物模型,但目前缺少一种能够模拟自然 HEV-3 感染的合适的小型动物模型。因此,我们用来源于野猪的 HEV-3 株对 C57BL/6 小鼠(野生型、IFNAR、CD4、CD8)和 BALB/c 裸鼠(nu/nu)、Wistar 大鼠和欧洲兔进行了实验性接种,并监测了病毒复制和排出情况,以及体液免疫反应。我们在接种的 8 只大鼠中检测到 1 只和 2 只大鼠以及所有的兔子的 HEV RNA 和抗 HEV 抗体,但在检测的任何一种小鼠品系中均未检测到。值得注意的是,对大鼠进行免疫抑制地塞米松处理并没有增强其对 HEV 感染的易感性。在兔子中,用重组 HEV-3 和大鼠 HEV 衣壳蛋白免疫接种可诱导对 HEV-3 攻击的保护。综上所述,兔的 HEV-3 感染模型可能是替代非人类灵长类动物和猪模型的合适选择,也是疫苗评价研究的合适基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8275/6356764/7be98d38cbd5/viruses-11-00001-g001.jpg

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