APOBEC3C S188I Polymorphism Enhances Context-Specific Editing of Hepatitis B Virus Genome

J Infect Dis. 2022 Sep 13;226(5):891-895. doi: 10.1093/infdis/jiac003.

Abstract

Single-nucleotide polymorphism in APOBEC3C (resulting in a serine to isoleucine in position 188) is present in approximately 10% of African populations and greatly enhances restriction against human immunodeficiency virus-1 and simian immunodeficiency virus by improving dimerization and DNA processivity of the enzyme. In this study, we demonstrated in culture and in infected patients that hepatitis B virus (HBV) could be edited by APOBEC3CS188I. Using next-generation sequencing, we demonstrated that APOBEC3CS188I led to enhanced editing activity in 5'TpCpA→5'TpTpA context. This constitutes a new hallmark of this enzyme, which could be used to determine its impact on HBV or nuclear DNA.

Keywords: APOBEC3C; Africa; editing; hepatitis B virus; nucleotide context; patients; polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytidine Deaminase* / genetics
  • Genome, Viral*
  • Hepatitis B / genetics
  • Hepatitis B virus* / genetics
  • Humans
  • Polymorphism, Single Nucleotide

Substances

  • APOBEC3C protein, human
  • Cytidine Deaminase