Panajotov Jessica, Falkenhagen Alexander, Gadicherla Ashish K, Johne Reimar
German Federal Institute for Risk Assessment, 10589 Berlin, Germany.
German Federal Institute for Risk Assessment, 10589 Berlin, Germany; Center for Quantitative Cell Imaging, University of Wisconsin, Madison, USA.
Virus Res. 2024 Jun;344:199364. doi: 10.1016/j.virusres.2024.199364. Epub 2024 Mar 28.
The hepatitis E virus (HEV) can cause acute and chronic hepatitis in humans. Whereas HEV genotypes 1-4 of species Paslahepevirus balayani are commonly found in humans, infections with ratHEV (species Rocahepevirus ratti) were previously considered to be restricted to rats. However, several cases of human ratHEV infections have been described recently. To investigate the zoonotic potential of this virus, a genomic clone was constructed here based on sequence data of ratHEV strain pt2, originally identified in a human patient with acute hepatitis from Hongkong. For comparison, genomic clones of ratHEV strain R63 from a rat and of HEV genotype 3 strain 47832mc from a human patient were used. After transfection of in vitro-transcribed RNA from the genomic clones into the human hepatoma cell line HuH-7-Lunet BLR, virus replication was shown for all strains by increasing genome copy numbers in cell culture supernatants. These cells developed persistent virus infections, and virus particles in the culture supernatant as well as viral antigen within the cells were demonstrated. All three generated virus strains successfully infected fresh HuH-7-Lunet BLR cells. In contrast, the human hepatoma cell lines HuH-7 and PLC/PRF/5 could only be infected with the genotype 3 strain and to a lesser extent with ratHEV strain R63. Infection of the rat-derived hepatoma cell lines clone 9, MH1C1 and H-4-II-E did not result in efficient virus replication for either strain. The results indicate that ratHEV strains from rats and humans can infect human hepatoma cells. The replication efficiency is strongly dependent on the cell line and virus strain. The investigated rat hepatoma cell lines could not be infected and other rat-derived cells should be tested in future to identify permissive cell lines from rats. The developed genomic clone can represent a useful tool for future research investigating pathogenicity and zoonotic potential of ratHEV.
戊型肝炎病毒(HEV)可导致人类急性和慢性肝炎。帕斯拉肝炎病毒属的HEV基因型1 - 4在人类中较为常见,而大鼠HEV(罗卡肝炎病毒属)感染以前被认为仅限于大鼠。然而,最近已报道了几例人类感染大鼠HEV的病例。为了研究这种病毒的人畜共患病潜力,我们基于最初在一名来自香港的急性肝炎患者中鉴定出的大鼠HEV毒株pt2的序列数据构建了一个基因组克隆。作为对照,使用了来自大鼠的大鼠HEV毒株R63和来自一名人类患者的HEV基因型3毒株47832mc的基因组克隆。将基因组克隆体外转录的RNA转染到人肝癌细胞系HuH - 7 - Lunet BLR后,通过增加细胞培养上清液中的基因组拷贝数,显示所有毒株均能进行病毒复制。这些细胞形成了持续性病毒感染,并在培养上清液中检测到病毒颗粒以及细胞内的病毒抗原。所有三种产生的病毒毒株均成功感染了新鲜的HuH - 7 - Lunet BLR细胞。相比之下,人肝癌细胞系HuH - 7和PLC/PRF/5仅能被基因型3毒株感染,且被大鼠HEV毒株R63感染的程度较低。大鼠来源的肝癌细胞系克隆9、MH1C1和H - 4 - II - E对这两种毒株均未产生有效的病毒复制。结果表明,来自大鼠和人类的大鼠HEV毒株均可感染人肝癌细胞。复制效率强烈依赖于细胞系和病毒毒株。所研究的大鼠肝癌细胞系未被感染,未来应测试其他大鼠来源的细胞以鉴定大鼠的允许性细胞系。所构建的基因组克隆可为未来研究大鼠HEV的致病性和人畜共患病潜力提供有用的工具。