# Molecular Characterization of Hepatitis B Virus in People Living with HIV in Rural and Peri-Urban Communities in Botswana

**Authors:** Bonolo B. Phinius, Wonderful T. Choga, Motswedi Anderson, Margaret Mokomane, Irene Gobe, Tsholofelo Ratsoma, Basetsana Phakedi, Gorata Mpebe, Lynnette Bhebhe, Tendani Gaolathe, Mosepele Mosepele, Joseph Makhema, Roger Shapiro, Shahin Lockman, Rosemary Musonda, Sikhulile Moyo, Simani Gaseitsiwe

PMC · DOI: 10.3390/biomedicines12071561 · Biomedicines · 2024-07-14

## TL;DR

This study analyzed hepatitis B virus (HBV) in people with HIV in Botswana, finding common mutations and differences over time.

## Contribution

The study provides new molecular insights into HBV evolution in HIV-positive individuals in Botswana.

## Key findings

- Sequencing success was higher in HBsAg+ samples compared to OBI+ samples.
- Most HBV sequences were genotype A1, with some D3 and E genotypes identified.
- Escape mutations like K122R were common, and some mutations affected protein function.

## Abstract

(1) Background: Hepatitis B virus (HBV) sequencing data are important for monitoring HBV evolution. We aimed to molecularly characterize HBV sequences from participants with HBV surface antigen-positive (HBsAg+) serology and occult hepatitis B infection (OBI+). (2) Methods: We utilized archived plasma samples from people living with human immunodeficiency virus (PLWH) in Botswana. HBV DNA was sequenced, genotyped and analyzed for mutations. We compared mutations from study sequences to those from previously generated HBV sequences in Botswana. The impact of OBI-associated mutations on protein function was assessed using the Protein Variation Effect Analyzer. (3) Results: Sequencing success was higher in HBsAg+ than in OBI+ samples [86/128 (67.2%) vs. 21/71 (29.2%)]. Overall, 93.5% (100/107) of sequences were genotype A1, 2.8% (3/107) were D3 and 3.7% (4/107) were E. We identified 13 escape mutations in 18/90 (20%) sequences with HBsAg coverage, with K122R having the highest frequency. The mutational profile of current sequences differed from previous Botswana HBV sequences, suggesting possible mutational changes over time. Mutations deemed to have an impact on protein function were tpQ6H, surfaceV194A and preCW28L. (4) Conclusions: We characterized HBV sequences from PLWH in Botswana. Escape mutations were prevalent and were not associated with OBI. Longitudinal HBV studies are needed to investigate HBV natural evolution.

## Linked entities

- **Diseases:** Hepatitis B (MONDO:0005344)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** hepatitis B infection (MESH:D006509), human immunodeficiency virus (MESH:D015658)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Human immunodeficiency virus 1 (no rank) [taxon 11676]
- **Mutations:** K122R

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11275055/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11275055/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC11275055/full.md

---
Source: https://tomesphere.com/paper/PMC11275055