Abstract

BackgroundHepatitis B virus (HBV) can have mutations that include the a determinant, which causes breakthrough infection. In particular, a single mutation at amino acid 145 of the surface protein (G145) is frequently reported in the failure of prophylactic treatment. The aim of this study was to evaluate the frequency of the a determinant mutants, especially the G145 variant, in Japan, where universal vaccination has not been adopted.MethodsThe present study was a retrospective study. The study cohorts were defined as follows: group 1, children with failure to prevent mother-to-child transmission despite immunoprophylaxis (n = 18, male/female = 8/10, age 1-14 years; median 6 years); group 2, HBV carriers who had not received vaccination or hepatitis B immunoglobulin (n = 107, male/female = 107, age 1-52 years; median 16 years). To detect the G145R and G145A mutants in patients, we designed 3 probes for real-time PCR. We also performed direct sequencing and cloning of PCR products.ResultsBy mutant-specific real-time PCR, one subject (5.6%) was positive for the G145R mutant in group 1, while the G145 mutant was undetectable in group 2. The a determinant mutants were detected in one (5.6%) of the group 1 subjects and 10 (9.3%) of the group 2 subjects using direct sequencing, but direct sequencing did not reveal the G145 mutant as a predominant strain in the two groups. However, the subject who was positive according to the mutant-specific real-time PCR in group 1 had overlapped peaks at nt 587 in the electropherogram. In group 2, 11 patients had overlapped peaks at nt 587 in the electropherogram. Cloning of PCR products allowed detection of the G145R mutant as a minor strain in 7 (group 1: 1 subject, group 2: 6 subjects) of 12 subjects who had overlapped peaks at nt 587 in the electropherogram.ConclusionsThe frequency of the a determinant mutants was not high in Japan. However, the G145R mutant was often present as a minor population in children and adults. HBV carriers might have the a determinant mutants as a minor form.

Highlights

  • Hepatitis B virus (HBV) can have mutations that include the a determinant, which causes breakthrough infection

  • The mutant primer detected a weak signal of wild-type HBV DNA, these findings suggested that the mutant primer could clearly identify the mutant with a point mutation at nt 587 G to A if the mutant was the predominant strain

  • HBV carriers without HB immunoglobulin (HBIG) or the HB vaccine We examined 107 HBV carriers who had never received HBIG or the HB vaccine and found that none of them was positive for the mutant-specific real-time polymerase chain reaction (PCR) (Table 2)

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Summary

Introduction

Hepatitis B virus (HBV) can have mutations that include the a determinant, which causes breakthrough infection. The aim of this study was to evaluate the frequency of the a determinant mutants, especially the G145 variant, in Japan, where universal vaccination has not been adopted. Hepatitis B virus (HBV) variants with mutations in the a determinant frequently emerge under immunological pressure induced by the HB vaccine or HB immunoglobulin (HBIG)[1,2,3,4]. Of various mutants with the a determinant, the mutant with a single mutation at the 145th amino acid of the hepatitis B surface antigen (HBsAg) has been frequently reported to cause the failure of prophylaxis in mother-to-child transmission [5,6,7,8,9,10]. The aim of this study was to evaluate the frequency of the a determinant mutants in HBV carriers

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