The genetic variability of hepatitis B virus subgenotype F1b precore/core gene is related to the outcome of the acute infection

ESPOSITO, ISABELLA; MENDIZABAL, MANUEL; CALZETTA, PABLO; GADANO, ADRIÁN; MARCIANO, SEBASTIÁN; MASCARDI, MARIA FLORENCIA; ARRIGO, DIEGO; GIUNTA, DIEGO; MARCIANO, SEBASTIÁN; MASCARDI, MARIA FLORENCIA; ARRIGO, DIEGO; GIUNTA, DIEGO; TRINKS, JULIETA; FRANCO, ALEJANDRA; LIVELLARA, BEATRIZ; VUJACICH, CLAUDIA; FLICHMAN, DIEGO; TRINKS, JULIETA; FRANCO, ALEJANDRA; LIVELLARA, BEATRIZ; VUJACICH, CLAUDIA; FLICHMAN, DIEGO; ESPOSITO, ISABELLA; MENDIZABAL, MANUEL; CALZETTA, PABLO; GADANO, ADRIÁN

VIRUS RESEARCH

ELSEVIER SCIENCE BV

Año: 2020 vol. 277

0168-1702

Aim: To assess the association of viral and host genetic variability with the outcome of acute infection with hepatitis B virus subgenotype F1b (HBV/F1b). Methods: The cohort consisted of 26 patients with acute HBV/F1b infection who exhibit different outcomes: spontaneous resolution (n = 10), progression to chronic hepatitis (n = 10) and acute liver failure (n = 6). HLA SNPs (rs3077, rs9277542, rs2856718 and rs7453920) were determined. The S gene and core promoter/precore/core region were direct sequenced, and this latter region was also ultra-deep sequenced. Mean number of mutations, mutation rate, Shannon entropy, positive selection sites and mutational patterns of quasispecies were compared between groups. Results: HLA SNPs were associated with spontaneous resolution or progression to chronic hepatitis, but not with the development of acute liver failure. The mean number of mutations in the S gene was similar among the three groups. Patients with spontaneous resolution had the lowest number of mutations, mutation rates and Shannon entropy values in the precore/core compared to the other two groups. Ten positive selection sites mapped on HLA-restricted epitopes were related to progression to chronic hepatitis and acute liver failure. Mutations T1753C, A1762T, G1764A, C1766T, T1768A G1896A, G2092T and T2107C were associated with acute liver failure and progression to chronic hepatitis. Conclusion: Highly heterogeneous and complex HBV precore/core carrying specific point mutations, combined with the host HLA background, were associated with a worse clinical outcome of acute HBV/F1b infection.