Department of Microbiology and Infectious Disease Centre, School of Basic Medical Sciences, Peking University Health Science Centre, Beijing, People's Republic of China.
Department of Severe Hepatology, Shanghai Public Health Clinical Centre, Fudan University, Shanghai, People's Republic of China.
Emerg Microbes Infect. 2020 Dec;9(1):2697-2705. doi: 10.1080/22221751.2020.1858178.
The pathogenicity of each hepatitis E virus (HEV) genotypes/subtypes may be different. This study aimed to investigate the infectivity and pathogenicity of different HEV genotypes/subtypes from different mammalian sources especially human in rabbits, and to assess whether rabbits are an appropriate animal model to study different HEV genotypes/subtypes. Thirty-seven rabbits were randomly divided into nine groups and inoculated with eight different HEV strains, including human-derived HEV3b (hHEV-3b), hHEV-4a, hHEV-4d and hHEV-4h, swine-derived HEV4d (sHEV-4d) and sHEV-4h, rabbit-derived HEV3 (HEV-3ra) and camel-derived HEV8. HEV RNA, antigen, anti-HEV and alanine aminotransferase (ALT) in serum or/and feces were monitored weekly. One rabbit from each group was euthanized at seven weeks post inoculation and the liver specimens were taken for histopathological analysis and immunofluorescence staining of HEV ORF2 proteins. hHEV-4d, sHEV-4d and HEV-3ra infections were successfully established in rabbits and typical acute hepatitis symptoms were observed, including viraemia/antigenemia, fecal virus/antigen shedding, elevated ALT level and liver histopathological changes. One rabbit infected with HEV-3ra showed chronic infection. hHEV-4d and sHEV-4d are less infectious and pathogenic than HEV-3ra in rabbits. hHEV-3b and HEV8 only caused inapparent infection in rabbits as 60% (3/5) and 20% (1/5) of the rabbits seroconverted to anti-HEV, respectively. No obvious signs of HEV infection in rabbits inoculated with hHEV-4a, hHEV-4h and sHEV-4h. The infectivity and pathogenicity of different HEV genotypes/subtypes in rabbits is different, which may be related to the species specificity of HEV. Rabbit can be used as an animal model for the study of HEV-3ra and more importantly human HEV-4d.
各型/亚型戊型肝炎病毒(HEV)的致病性可能不同。本研究旨在探索来自不同哺乳动物来源(尤其是人类)的不同 HEV 基因型/亚型在兔体内的感染性和致病性,并评估兔是否为研究不同 HEV 基因型/亚型的合适动物模型。37 只兔随机分为 9 组,接种 8 种不同的 HEV 株,包括人源 HEV3b(hHEV-3b)、hHEV-4a、hHEV-4d 和 hHEV-4h、猪源 HEV4d(sHEV-4d)和 sHEV-4h、兔源 HEV3(HEV-3ra)和骆驼源 HEV8。每周监测血清或/和粪便中的 HEV RNA、抗原、抗-HEV 和丙氨酸氨基转移酶(ALT)。每组各有 1 只兔在接种后 7 周处死,取肝脏标本进行组织病理学分析和 HEV ORF2 蛋白免疫荧光染色。hHEV-4d、sHEV-4d 和 HEV-3ra 感染兔成功建立,观察到典型的急性肝炎症状,包括病毒血症/抗原血症、粪便病毒/抗原排出、ALT 水平升高和肝组织病理学改变。1 只感染 HEV-3ra 的兔出现慢性感染。与 HEV-3ra 相比,hHEV-4d 和 sHEV-4d 在兔体内的感染性和致病性较低。hHEV-3b 和 HEV8 仅使 60%(3/5)和 20%(1/5)的兔血清转换为抗-HEV,导致无症状感染。接种 hHEV-4a、hHEV-4h 和 sHEV-4h 的兔未出现明显的 HEV 感染迹象。不同 HEV 基因型/亚型在兔体内的感染性和致病性不同,这可能与 HEV 的种属特异性有关。兔可作为研究 HEV-3ra 的动物模型,更重要的是可作为研究人源 HEV-4d 的动物模型。