Production of infectious dromedary camel hepatitis E virus by a reverse genetic system: Potential for zoonotic infection

被引:50
|
作者
Li, Tian-Cheng [1 ]
Zhou, Xianfeng [3 ]
Yoshizaki, Sayaka [1 ]
Ami, Yasushi [2 ]
Suzaki, Yuriko [2 ]
Nakamura, Tomofumi [4 ]
Takeda, Naokazu [5 ]
Wakita, Takaji [1 ]
机构
[1] Natl Inst Infect Dis, Dept Virol 2, Gakuen 4-7-1, Tokyo 2080011, Japan
[2] Natl Inst Infect Dis, Div Expt Anim Res, Gakuen 4-7-1, Tokyo 2080011, Japan
[3] Nanchang Ctr Dis Control & Prevent, Dept Microbiol, Nanchang, Jiangxi, Peoples R China
[4] Osaka Univ, Res Fdn Microbial Dis, Kanonji Inst, Seto Ctr, Seto Cho 4-1-70, Kanonji, Kagawa 7680065, Japan
[5] Osaka Univ, Microbial Dis Res Inst, Suita, Osaka 5650781, Japan
关键词
Dromedary camel hepatitis E virus; DcHEV; Zoonotic infection; Alanine aminotransferase (ALT); Reverse genetics system; PLC/PRF/5; cell; FAMILY HEPEVIRIDAE; CDNA-CLONE; HEV; CONSTRUCTION; PARTICLES; PREGNANCY; STRAINS; GENOME; FECES; SWINE;
D O I
10.1016/j.jhep.2016.07.013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: The pathogenicity, epidemiology and replication mechanism of dromedary camel hepatitis E virus (DcHEV), a novel hepatitis E virus (HEV), has been unclear. Here we used a reverse genetic system to produce DcHEV and examined the possibility of zoonotic infection. METHODS: Capped genomic RNA derived from a synthetic DcHEV cDNA was transfected into human hepatocarcinoma cells PLC/PRF/5. The DcHEV capsid protein and RNA were detected by an enzyme-linked immunosorbent assay (ELISA) or RT-qPCR. A neutralization test for DcHEV was carried out by using antisera against HEV-like particles. DcHEV was used to inoculate two cynomolgus monkeys to examine the potential for cross-species infection. RESULTS: The transfection of PLC/PRF/5 cells with capped DcHEV RNA resulted in the production of infectious DcHEV. The genome sequence analysis demonstrated that both nucleotide and amino acid changes accumulated during the passages in PLC/PRF/5 cells. The cynomolgus monkeys showed serological signs of infection when DcHEV was intravenously inoculated. DcHEV was neutralized by not only anti-DcHEV-LPs antibody, but also anti-genotype 1 (G1), G3 and G4 HEV-LPs antibodies. Moreover, the monkeys immunized with DcHEV escaped the G3 HEV challenge, indicating that the serotype of DcHEV is similar to those of other human HEVs. CONCLUSIONS: Infectious DcHEV was produced using a reverse genetic system and propagated in PLC/PRF/5 cells. The antigenicity and immunogenicity of DcHEV are similar to those of G1, G3 and G4 HEV. DcHEV was experimentally transmitted to primates, demonstrating the possibility of a zoonotic infection by DcHEV. LAY SUMMARY: Dromedary camel hepatitis E virus (DcHEV) was produced by a reverse genetic system and grows well in PLC/PRF/5 cells. Cynomolgus monkeys experimentally infected with DcHEV indicated serological signs of infection, suggesting that DcHEV has the potential to cause zoonotic HEV infection. (C) 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved
引用
收藏
页码:1104 / 1111
页数:8
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