Tracing 2500 years of human betaherpesvirus 6A and 6B diversity through ancient DNA
Guellil MPapers in this archive, van Dorp LPapers in this archive, Saag LPapers in this archive, Beneker OPapers in this archive, Bonucci BPapers in this archive, Sasso SPapers in this archive, Saupe TPapers in this archive, Solnik APapers in this archive, Kabral HPapers in this archive, Allmäe RPapers in this archive, Bates JPapers in this archive, Dittmar JMPapers in this archive, Ge XJPapers in this archive, Inskip SPapers in this archive, Jonuks TPapers in this archive, Karmanov VNPapers in this archive, Khartanovich VIPapers in this archive, Larmuseau MHDPapers in this archive, Aneli SPapers in this archive, Cessford CPapers in this archive, Kriiska APapers in this archive, Mägi MPapers in this archive, Malve MPapers in this archive, De Winter NPapers in this archive, Metspalu MPapers in this archive, Pagani LPapers in this archive, Robb JEPapers in this archive, Kivisild TPapers in this archive, H
Abstract
Human betaherpesviruses 6A and 6B (HHV-6A/6B) are DNA viruses, which integrate into the human genome, and are best known to cause “sixth disease.” Despite their recent discovery (1980s), they were speculated to have a much longer history within the human population than modern data suggest. We present the first 11 ancient genomes of HHV-6A and HHV-6B, dating as far back as the 8th to 6th century BCE. We demonstrate that large fractions of current HHV-6 diversity were already established by the 14th century CE. Our data corroborate that HHV-6A/6B integrations stem from ancient founder events. In addition, we show that all known inherited chromosomally integrated HHV-6A clades were already represented in historical populations, confirming that HHV-6A no longer integrates into the germ line within populations of European ancestry and likely endogenized in early human history.
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