Strain- and Subtype-Specific Replication of Genotype 3 Hepatitis E Viruses in Mongolian Gerbils

Tiancheng Li1, Yusuke Sakai2, Yasushi Ami3

  • 1Department of Virology II, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.

Viruses
|October 26, 2024
PubMed

Insights

Mongolian gerbils show potential as a small animal model for Hepatitis E Virus genotype 3 (HEV-3) infections, with infectivity varying by subtype. HEV-4i and HEV-5 infected gerbils may serve as models for studying HEV pathogenicity.

Area of Science:

  • Virology
  • Infectious Diseases
  • Animal Models

Background:

  • Mongolian gerbils are susceptible to various Hepatitis E Virus (HEV) genotypes (1, 4, 5, 8) and rat HEV, establishing them as a small animal model.
  • HEV genotype 3 (HEV-3) is a significant cause of zoonotic HEV infections, yet its subtypes HEV-3k and HEV-3ra show limited infectivity in gerbils.
  • A robust small-animal model for HEV-3 is crucial for understanding and combating zoonotic HEV.

Purpose of the Study:

  • To evaluate the infectivity of different HEV-3 subtypes in Mongolian gerbils.
  • To determine the potential of gerbils as a small-animal model for HEV-3 infections.
  • To compare the pathogenicity of various HEV strains and genera in gerbils.

Main Methods:

  • Gerbils were inoculated with five HEV-3 subtypes (HEV-3b, -3e, -3f, -3k, and -3ra).
  • Viral RNA detection in feces and anti-HEV IgG antibody titers in serum were analyzed.
  • ALT levels and liver damage were assessed following infection with HEV-3e, HEV-4i, HEV-5, and rat HEV.

Main Results:

  • Viral RNA was detected in the feces of gerbils infected with all tested HEV-3 subtypes.
  • High anti-HEV IgG antibody titers were observed in gerbils infected with HEV-3b/ch-, HEV-3f-, and HEV-3e.
  • HEV-3e infection led to prolonged high-level fecal virus shedding; HEV-3k and HEV-3ra showed limited replication and antibody response.
  • HEV-4i and HEV-5 infections caused elevated ALT levels and liver damage, unlike HEV-3e and rat HEV infections.

Conclusions:

  • Mongolian gerbils demonstrate potential as a small-animal model for HEV-3, with infectivity and host response varying by subtype and strain.
  • HEV-3e-infected gerbils are a promising model for studying HEV-3 shedding.
  • Gerbils infected with HEV-4i and HEV-5 may serve as valuable models for investigating HEV pathogenicity.