# Experimental hepatitis E virus genotype 1 infection in three types of wild rodents

**Authors:** He Zhang, Yang Wu, Haojie Wang, Tianxu Liu, Xing Liu, Jianxing Chen, Yue Sun, Lihong Xue, Changwen Li, Huairan Liu, Hongyan Chen, Yinglin Qi, Tongqing An, Liang Wang, Zhimin Jin, Changqing Yu, Xinyue Yang, Yuebao Li, Hui Li, Changyou Xia, Xin Yin, Lin Wang

PMC · DOI: 10.1371/journal.ppat.1014050 · 2026-03-18

## TL;DR

Researchers found that three wild rodent species can be infected with a human-specific hepatitis E virus, suggesting these animals might play a role in virus spread.

## Contribution

The study identifies wild rodents as potential natural hosts for HEV-1, challenging the belief that the virus is strictly human-specific.

## Key findings

- Apodemus peninsulae showed high susceptibility to HEV-1 with symptoms similar to human infections.
- Infected rodents exhibited systemic viral replication and activated inflammatory pathways like IL-1β and IL-18.
- HEV-1 can be transmitted through oral, contact, and vertical routes in these rodents, with ribavirin effective in suppressing replication.

## Abstract

Hepatitis E virus genotype 1 (HEV-1) has long been considered human-specific, with no known natural animal hosts. Here, we demonstrate that three wild rodent species—Apodemus peninsulae, Clethrionomys rufocanus, and Lasiopodomys brandtii—are susceptible to HEV-1 infection. Among them, A. peninsulae infected with HEV-1 exhibited the highest susceptibility, characterized by robust fecal viral shedding, systemic viral replication, seroconversion, and mild liver pathology mimicking human acute HEV-1 infection. Intrahepatic transcriptomic analysis of infected animals revealed activation of inflammatory pathways, including upregulation of IL-1β and IL-18. Re-inoculation experiments confirmed infection-induced protective immunity, and ribavirin treatment effectively suppressed viral replication. HEV-1 infection can be established by oral gavage inoculation, close contact and vertical transmission. These results provide solid evidence that wild rodents can serve as potential hosts for HEV-1, highlighting the potential role of wild rodents in HEV-1 ecology and cross-species transmission.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL18 (interleukin 18)
- **Chemicals:** ribavirin (PubChem CID 37542)
- **Species:** Apodemus peninsulae (taxon 105297), Lasiopodomys brandtii (taxon 407171)

## Full-text entities

- **Genes:** IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, ORF2 [NCBI Gene 1494410], IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** viremia (MESH:D014766), Infection (MESH:D007239), HEV (MESH:D016751), inflammatory (MESH:D007249), weight gain (MESH:D015430), hepatic injury (MESH:D056486), zoonotic (MESH:D015047), AHE (MESH:D017114)
- **Chemicals:** sodium phosphate (MESH:C018279), eosin (MESH:D004801), Ribavirin (MESH:D012254), DAB (MESH:C000469), TRIzol (MESH:C411644), ammonium molybdate (MESH:C022175), iodixanol (MESH:C044834), xylene (MESH:D014992), agarose (MESH:D012685), BioRender (-), ethanol (MESH:D000431), carbon (MESH:D002244), phosphotungstic acid (MESH:D010772), sucrose (MESH:D013395), glutaraldehyde (MESH:D005976), hematoxylin (MESH:D006416), water (MESH:D014867), Formvar (MESH:C013215), copper (MESH:D003300), formalin (MESH:D005557), paraffin (MESH:D010232), H&amp;E (MESH:D006371), remdesivir (MESH:C000606551)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009], C. rufocanus [taxon 527686], Apodemus peninsulae (Korean field mouse, species) [taxon 105297], Gerbillinae (gerbils, subfamily) [taxon 10045], Rodentia (rodent, order) [taxon 9989], Mus musculus (house mouse, species) [taxon 10090], Meriones unguiculatus (Mongolian gerbil, species) [taxon 10047], Sus scrofa (pig, species) [taxon 9823], Lasiopodomys brandtii (Brandt's vole, species) [taxon 407171], Hepatitis E Virus [taxon 12461], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** alanine (A) at position 462, Histidine (H) at position 458, S10A, Y1320H, S11A, valine (V) at position 600

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12998826/full.md

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Source: https://tomesphere.com/paper/PMC12998826