Expanding the Hepatitis E Virus Toolbox: Selectable Replicons and Recombinant Reporter Genomes

Viruses. 2023 Mar 28;15(4):869. doi: 10.3390/v15040869.

Abstract

Hepatitis E virus (HEV) has received relatively little attention for decades although it is now considered as one of the most frequent causes of acute hepatitis worldwide. Our knowledge of this enterically-transmitted, positive-strand RNA virus and its life cycle remains scarce but research on HEV has gained momentum more recently. Indeed, advances in the molecular virology of hepatitis E, including the establishment of subgenomic replicons and infectious molecular clones, now allow study of the entire viral life cycle and to explore host factors required for productive infection. Here, we provide an overview on currently available systems, with an emphasis on selectable replicons and recombinant reporter genomes. Furthermore, we discuss the challenges in developing new systems which should enable to further investigate this widely distributed and important pathogen.

Keywords: epitope tag; infectious clone; insertion; reporter; selection gene; subgenomic replicon.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genome, Viral
  • Hepatitis E virus* / genetics
  • Hepatitis E*
  • Humans
  • RNA, Viral
  • Replicon
  • Virus Replication / genetics

Substances

  • RNA, Viral

Grants and funding

This research was funded by the Swiss National Science Foundation (grants 310030_207477 and CRSK-3_190706) as well as the Novartis Foundation for Medical–Biological Research (grant 18C140).