Human hepatocytes apoptosis induced by replication of hepatitis B virus subgenotypes F1b and F4: Role of basal core promoter and preCore mutations

SEVIC, INA; BARBINI, LUCIANA; SEVIC, INA; BARBINI, LUCIANA; ELIZALDE, MARÍA MERCEDES; CAMPOS, RODOLFO HÉCTOR; GONZÁLEZ LÓPEZ LEDESMA, MARÍA MORA; ELIZALDE, MARÍA MERCEDES; FLICHMAN, DIEGO MARTIN; CAMPOS, RODOLFO HÉCTOR; GONZÁLEZ LÓPEZ LEDESMA, MARÍA MORA; FLICHMAN, DIEGO MARTIN

VIROLOGY

ACADEMIC PRESS INC ELSEVIER SCIENCE

Año: 2018 vol. 513 p. 160 - 167

0042-6822

In the context of pathogenesis of HBV infection, HBV genotypes and mutants have been shown to affect the natural course of chronic infection and treatment outcomes. In this work, we studied the induction of apoptosis by the replication of HBV subgenotypes F1b and F4, and the naturally occurring mutants BCP and preCore. Both subgenotypes F1b and F4 HBV genome transfections induced cell death by apoptosis in human hepatocytes. The BCPdm (A1762T/G1764A) and preCore (G1896A) mutants induced higher levels of apoptosis than the wt virus. This increase in apoptosis was not associated with the enhanced viral replication of the variants. HBV-mediated apoptosis was independent of viral subgenotypes, and associated with the modulation of members of the regulatory Bcl-2 family proteins expression in the mitochondrial apoptotic pathway. Finally, the apoptosis induction increase observed for the preCore mutants suggests that HBeAg might have an anti-apoptotic effect in human hepatocytes.