Molecular characterisation of a rabbit Hepatitis E Virus strain detected in a chronically HEV-infected individual from Germany

被引:2
|
作者
Klink, Patrycja [1 ]
Harms, Dominik [1 ,9 ]
Altmann, Britta [1 ]
Doerffel, Yvonne [2 ]
Morgera, Ulrike [2 ]
Zander, Steffen [1 ]
Bock, C. Thomas [1 ,3 ,8 ]
Hofmann, Joerg [4 ,5 ,6 ,7 ]
机构
[1] Robert Koch Inst, Dept Infect Dis, Div Viral Gastroenteritis & Hepatitis Pathogens &, D-13353 Berlin, Germany
[2] Charite Univ Med Berlin, Outpatient Clin, Berlin, Germany
[3] Univ Tubingen, Inst Trop Med, Tubingen, Germany
[4] Charite Univ Med Berlin, Inst Virol, Berlin, Germany
[5] Free Univ Berlin, Berlin, Germany
[6] Humboldt Univ, Berlin Inst Hlth, German Ctr Infect Res, Berlin, Germany
[7] Charite Vivantes GmbH, Lab Berlin, Berlin, Germany
[8] Robert Koch Inst, Seestr 10, D-13353 Berlin, Germany
[9] Inst Cardiac Diagnost & Therapy, Berlin, Germany
关键词
Rabbit HEV; Zoonoses; One health; NGS; Resistance-associated substitutions; Ribavirin; GENOTYPE; HUMANS; PIG;
D O I
10.1016/j.onehlt.2023.100528
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In immunocompromised individuals persisting viremia frequently leads to a chronic hepatitis E virus (HEV) infection. Zoonotic transmission of HEV from pigs and wild boar to humans is proven and sporadic infections with rabbit HEV (raHEV) have recently been reported. Here, the molecular characterisation of a raHEV strain isolated from an immunocompromised, chronically HEV-infected, heart-transplanted patient is described. After successful ribavirin (RBV) treatment of a HEV infection in 2019, the patient was again tested HEV positive in 2021 and received a second RBV therapy cycle. Full-length HEV genome amplification and next generation sequencing was performed on a plasma sample taken between first and second cycle of RBV therapy and a stool sample taken two months after starting the second cycle. The sequence of plasma (raHEV-83) and stool (raHEV99) derived virus showed the highest nucleotide sequence identity to a Chinese raHEV and a phylogenetic relationship to a raHEV strain isolated from a French patient. Furthermore, sequence analysis revealed the presence of RBV-associated substitutions V1479I and G1634K in the HEV sequences from plasma and additionally K1398R from stool. The results underline the role of rabbits as putative sources of HEV infection and emphasize the need of a one health concept for a better understanding of HEV epidemiology and to develop tools for prevention and control of HEV infection.
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