| Literature DB >> 29743673 |
Barbara Mühlemann1, Terry C Jones1,2, Peter de Barros Damgaard3, Morten E Allentoft3, Irina Shevnina4, Andrey Logvin4, Emma Usmanova5, Irina P Panyushkina6, Bazartseren Boldgiv7, Tsevel Bazartseren8, Kadicha Tashbaeva9, Victor Merz10, Nina Lau11, Václav Smrčka12, Dmitry Voyakin13, Egor Kitov14, Andrey Epimakhov15, Dalia Pokutta16, Magdolna Vicze17, T Douglas Price18, Vyacheslav Moiseyev19, Anders J Hansen3, Ludovic Orlando3,20, Simon Rasmussen21, Martin Sikora3, Lasse Vinner3, Albert D M E Osterhaus22, Derek J Smith1, Dieter Glebe23,24, Ron A M Fouchier25, Christian Drosten2,26, Karl-Göran Sjögren18, Kristian Kristiansen18, Eske Willerslev27,28,29.
Abstract
Hepatitis B virus (HBV) is a major cause of human hepatitis. There is considerable uncertainty about the timescale of its evolution and its association with humans. Here we present 12 full or partial ancient HBV genomes that are between approximately 0.8 and 4.5 thousand years old. The ancient sequences group either within or in a sister relationship with extant human or other ape HBV clades. Generally, the genome properties follow those of modern HBV. The root of the HBV tree is projected to between 8.6 and 20.9 thousand years ago, and we estimate a substitution rate of 8.04 × 10-6-1.51 × 10-5 nucleotide substitutions per site per year. In several cases, the geographical locations of the ancient genotypes do not match present-day distributions. Genotypes that today are typical of Africa and Asia, and a subgenotype from India, are shown to have an early Eurasian presence. The geographical and temporal patterns that we observe in ancient and modern HBV genotypes are compatible with well-documented human migrations during the Bronze and Iron Ages1,2. We provide evidence for the creation of HBV genotype A via recombination, and for a long-term association of modern HBV genotypes with humans, including the discovery of a human genotype that is now extinct. These data expose a complexity of HBV evolution that is not evident when considering modern sequences alone.Entities:
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Year: 2018 PMID: 29743673 DOI: 10.1038/s41586-018-0097-z
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962