Recombinant hepatitis E virus genomes infectious for primates: importance of capping and discovery of a cis-reactive element

Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15270-5. doi: 10.1073/pnas.251555098. Epub 2001 Dec 11.

Abstract

Hepatitis E virus recombinant genomes transcribed in vitro from two cDNA clones differing by two nucleotides were infectious for chimpanzees. However, one cDNA clone encoded a virus that was attenuated for chimpanzees and unable to infect rhesus monkeys. The second cDNA clone encoded a virus that infected both chimpanzees and rhesus monkeys and caused acute hepatitis in both. One mutation differentiating the two clones identified a cis-reactive element that appeared to overlap the 3' end of the capsid gene and part of the 3' noncoding region. Capping of the RNA transcripts was essential for infectivity.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • DNA, Viral
  • Genome, Viral*
  • Hepatitis E virus / genetics*
  • Hepatitis E virus / pathogenicity
  • Hepatitis, Viral, Animal / virology*
  • Macaca mulatta
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Pan troglodytes
  • RNA Caps*
  • RNA, Messenger / chemistry
  • RNA, Messenger / genetics
  • Recombination, Genetic*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Nucleic Acid
  • Virulence / genetics

Substances

  • DNA, Viral
  • RNA Caps
  • RNA, Messenger

Associated data

  • GENBANK/AF444002
  • GENBANK/AF444003