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Reduced genetic distance and high replication levels increase the RNA recombination rate of hepatitis delta virus

  • Chia Chi Lin
  • , Zhi Wei Yang
  • , Shan Bei Iang
  • , Mei Chao*
  • *Corresponding author for this work
  • Chang Gung University

Research output: Contribution to journalJournal Article peer-review

11 Scopus citations

Abstract

Hepatitis delta virus (HDV) replication is carried out by host RNA polymerases. Since homologous inter-genotypic RNA recombination is known to occur in HDV, possibly via a replication-dependent process, we hypothesized that the degree of sequence homology and the replication level should be related to the recombination frequency in cells co-expressing two HDV sequences. To confirm this, we separately co-transfected cells with three different pairs of HDV genomic RNAs and analyzed the obtained recombinants by RT-PCR followed by restriction fragment length polymorphism and sequencing analyses. The sequence divergence between the clones ranged from 24% to less than 0.1%, and the difference in replication levels was as high as 100-fold. As expected, significant differences were observed in the recombination frequencies, which ranged from 0.5% to 47.5%. Furthermore, varying the relative amounts of parental RNA altered the dominant recombinant species produced, suggesting that template switching occurs frequently during the synthesis of genomic HDV RNA. Taken together, these data suggest that during the host RNA polymerase-driven RNA recombination of HDV, both inter- and intra-genotypic recombination events are important in shaping the genetic diversity of HDV.

Original languageEnglish
Pages (from-to)79-85
Number of pages7
JournalVirus Research
Volume195
DOIs
StatePublished - 02 01 2015

Bibliographical note

Publisher Copyright:
© 2014 Elsevier B.V.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Hepatitis delta virus
  • RNA recombination
  • Template-switching
  • Viral evolution

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