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Detection of Low Copy Number Integrated Viral DNA Formed by In Vitro Hepatitis B Infection
Published on: November 7, 2018
Temporal evolution and global spread of hepatitis B virus genotype G
Jonas Michel Wolf1,2, Sílvia De Carli2, Vagner Reinaldo Zingalli Bueno Pereira2
1Programa de Pós-Graduação em Biologia Celular e Molecular Aplicada à Saúde, ULBRA, Universidade Luterana do Brasil, Canoas, Brazil.
Insights
Hepatitis B virus genotype G (HBV-G) originated in the 19th century, likely in North America. This rare HBV genotype spread globally in the late 20th century, with significant dissemination in the 1990s.
Area of Science:
- Virology
- Epidemiology
- Molecular Evolution
Background:
- Hepatitis B virus (HBV) infection is a significant global health concern.
- HBV is categorized into genotypes A-J, with varying worldwide prevalence.
- HBV genotype G (HBV-G) is rare but found across continents.
Purpose of the Study:
- To investigate the temporal evolution and global dissemination patterns of HBV genotype G.
- To compare whole-genome sequences of HBV-G from diverse geographical regions.
- To elucidate the origin and spread dynamics of HBV-G.
Main Methods:
- Bayesian coalescent analysis was employed.
- Estimated the time to the most recent common ancestor (tMRCA) for HBV-G.
- Analyzed population dynamics over recent decades.
Main Results:
- The tMRCA for all HBV-G strains was estimated to be around 1855 (HPD 95%: 1778-1931).
- HBV-G likely originated in North America and spread to other continents starting in the 1970s.
- Viral spread was constant from 1855 to the 1980s, increasing in the 1990s, and plateauing post-2000s.
Conclusions:
- HBV genotype G emerged in the 19th century.
- Major global spread events occurred in the late 20th century, particularly the 1990s.
- Dissemination in the 1990s may be linked to high-risk behaviors such as sexual activity and injecting drug use.
Abstract:
Hepatitis B virus (HBV) infection is considered a major health problem in the world. HBV is classified into genotypes A to J disseminated worldwide. Genotypes A, D and F are the most frequent in the Western World, B and C are predominant in the East, and E, F, H and J are infrequent and restricted to specific regions. HBV-G is a rare genotype, but it has been detected in different continents. This study aimed to report the temporal evolution and global spread of HBV-G comparing whole-genome sequences of this genotype from different regions in the world. Bayesian coalescent analysis was performed to estimate the time to the most recent common ancestor (tMRCA) and the population dynamics in the last decades. The results demonstrated that tMRCA of all HBV-Gs dated back to 1855 (95% highest posterior density interval [HPD 95%]: 1778 - 1931). This genotype has a possible origin in North America and it was disseminated to other continents (South and Central America, Europe, Asia and Africa) more than one century later (around the 1970s). The viral population demonstrated constant spreading from 1855 to the 1980s, followed by an increase in the 1990s and reached a plateau after the 2000s. Wide spreading at the beginning of the 1990s was probably associated with the dissemination by highly sexual active groups and injecting drug users. In conclusion, the present study demonstrated that HBV-G was originated in the 19th century with main events of spread at the end of the 20th century.
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