Cell binding tropism of rat hepatitis E virus is a pivotal determinant of its zoonotic transmission to humans

Classically, all hepatitis E virus (HEV) variants causing human infection belong to the genus <i>Paslahepevirus</i> (HEV-A). However, the increasing cases of rat HEV infection in humans since 2018 challenged this dogma, posing increasing health threats. Herein, we investigated the underlying mechanisms dictating the zoonotic potentials of different HEV species and their possible cross-protection relationships. We found that rat HEV virus-like particles (HEV<sup>VLPs</sup>) bound to human liver and intestinal cells/tissues with high efficiency. Moreover, rat HEV<sup>VLPs</sup> and infectious rat HEV particles penetrated the cell membrane and entered human target cells postbinding. In contrast, ferret HEV<sup>VLPs</sup> showed marginal cell binding and entry ability, bat HEV<sup>VLPs</sup> and avian HEV<sup>VLPs</sup> exhibited no binding and entry potency. Structure-based three-dimensional mapping identified that the surface spike domain of rat HEV is crucial for cell binding. Antigenic cartography indicated that rat HEV exhibited partial cross-reaction with HEV-A. Intriguingly, sera of HEV-A infected patients or human HEV vaccine Hecolin® immunized individuals provided partial cross-protection against the binding of rat HEV<sup>VLPs</sup> to human target cells. In summary, the interactions between the viral capsid and cellular receptor(s) regulate the distinct zoonotic potentials of different HEV species. The systematic characterization of antigenic cartography and serological cross-reactivity of different HEV species provide valuable insights for the development of species-specific diagnosis and protective vaccines against zoonotic HEV infection.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2024-10-28
DOI
https://doi.org/10.1073/pnas.2416255121
Citations
9
Primary Topic
Hepatitis Viruses Studies and Epidemiology
Type
article
Field-Weighted Citation Impact
3.33

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article

Cell binding tropism of rat hepatitis E virus is a pivotal determinant of its zoonotic transmission to humans

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9 citations
Proceedings of the National Academy of Sciences
Hepatitis Viruses Studies and Epidemiology
3.33
article

Cell binding tropism of rat hepatitis E virus is a pivotal determinant of its zoonotic transmission to humans

Lingli Wang, Siddharth Sridhar, Hongbo Guo, Yihan Lu, Xiucheng Pan, Zijie Wang, Renxian Tang, Jin Xu, Wenshi Wang, Huihui Kong, Jikai Zhang, Kuiyang Zheng, Guangde Yang, Jianwen Situ, Ying Dong, Zizheng Zheng, Xiaohui Ding, Peng Zhou, Jia Su, Chunyang Li, Zheng Li, Yao Hou, Shusheng Wu, Yibo Ding, Weiwei Miao, Dou Zeng, Xia Wang
article en
9 citations

Abstract

Classically, all hepatitis E virus (HEV) variants causing human infection belong to the genus <i>Paslahepevirus</i> (HEV-A). However, the increasing cases of rat HEV infection in humans since 2018 challenged this dogma, posing increasing health threats. Herein, we investigated the underlying mechanisms dictating the zoonotic potentials of different HEV species and their possible cross-protection relationships. We found that rat HEV virus-like particles (HEV<sup>VLPs</sup>) bound to human liver and intestinal cells/tissues with high efficiency. Moreover, rat HEV<sup>VLPs</sup> and infectious rat HEV particles penetrated the cell membrane and entered human target cells postbinding. In contrast, ferret HEV<sup>VLPs</sup> showed marginal cell binding and entry ability, bat HEV<sup>VLPs</sup> and avian HEV<sup>VLPs</sup> exhibited no binding and entry potency. Structure-based three-dimensional mapping identified that the surface spike domain of rat HEV is crucial for cell binding. Antigenic cartography indicated that rat HEV exhibited partial cross-reaction with HEV-A. Intriguingly, sera of HEV-A infected patients or human HEV vaccine Hecolin® immunized individuals provided partial cross-protection against the binding of rat HEV<sup>VLPs</sup> to human target cells. In summary, the interactions between the viral capsid and cellular receptor(s) regulate the distinct zoonotic potentials of different HEV species. The systematic characterization of antigenic cartography and serological cross-reactivity of different HEV species provide valuable insights for the development of species-specific diagnosis and protective vaccines against zoonotic HEV infection.

Proceedings of the National Academy of SciencesVol. 121(45)
Xuzhou Medical College (CN), Xiamen University (CN), Chinese Academy of Sciences (CN), Fudan University (CN), Guangzhou Experimental Station (CN), Wuhan Institute of Virology (CN), Chinese Academy of Agricultural Sciences (CN), Harbin Veterinary Research Institute (CN), University of Hong Kong (HK)
Jiangsu Commission of Health, National Natural Science Foundation of China, Food and Health Bureau, Xuzhou Medical University, Health and Medical Research Fund, Li Ka Shing Faculty of Medicine, University of Hong Kong
Life in Land
Openalex Percentile: Top 7%
Hepatitis Viruses Studies and Epidemiology
3.33
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