<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Tweedy J</submitter><funding>HHV-6 Foundation</funding><pubmed_abstract>Human herpesvirus-6A and B (HHV-6A, HHV-6B) have recently defined endogenous genomes, resulting from integration into the germline: chromosomally-integrated "CiHHV-6A/B". These affect approximately 1.0% of human populations, giving potential for virus gene expression in every cell. We previously showed that CiHHV-6A was more divergent than CiHHV-6B by examining four genes in 44 European CiHHV-6A/B cardiac/haematology patients. There was evidence for gene expression/reactivation, implying functional non-defective genomes. To further define the relationship between HHV-6A and CiHHV-6A we used next-generation sequencing to characterize genomes from three CiHHV-6A cardiac patients. Comparisons to known exogenous HHV-6A showed CiHHV-6A genomes formed a separate clade; including all 85 non-inter</pubmed_abstract><journal>Viruses</journal><pagination>E19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4728579</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Complete Genome Sequence of Germline Chromosomally Integrated Human Herpesvirus 6A and Analyses Integration Sites Define a New Human Endogenous Virus with Potential to Reactivate as an Emerging Infection.</pubmed_title><pmcid>PMC4728579</pmcid><pubmed_authors>Lassner D</pubmed_authors><pubmed_authors>Tweedy J</pubmed_authors><pubmed_authors>Spyrou MA</pubmed_authors><pubmed_authors>Kuhl U</pubmed_authors><pubmed_authors>Pearson M</pubmed_authors><pubmed_authors>Gompels UA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Complete Genome Sequence of Germline Chromosomally Integrated Human Herpesvirus 6A and Analyses Integration Sites Define a New Human Endogenous Virus with Potential to Reactivate as an Emerging Infection.</name><description>Human herpesvirus-6A and B (HHV-6A, HHV-6B) have recently defined endogenous genomes, resulting from integration into the germline: chromosomally-integrated "CiHHV-6A/B". These affect approximately 1.0% of human populations, giving potential for virus gene expression in every cell. We previously showed that CiHHV-6A was more divergent than CiHHV-6B by examining four genes in 44 European CiHHV-6A/B cardiac/haematology patients. There was evidence for gene expression/reactivation, implying functional non-defective genomes. To further define the relationship between HHV-6A and CiHHV-6A we used next-generation sequencing to characterize genomes from three CiHHV-6A cardiac patients. Comparisons to known exogenous HHV-6A showed CiHHV-6A genomes formed a separate clade; including all 85 non-inter</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2026-05-05T18:58:48.397Z</modification><creation>2019-03-27T02:07:38Z</creation></dates><accession>S-EPMC4728579</accession><cross_references><pubmed>26784220</pubmed><doi>10.3390/v8010019</doi></cross_references></HashMap>