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Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin

Human herpesviruses 6-A and -B (HHV-6A, HHV-6B) are ubiquitous in human populations worldwide. These viruses have been associated with several diseases such as multiple sclerosis, Hodgkin’s lymphoma or encephalitis. Despite of the need to understand the genetic diversity and geographic stratificatio...

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Autores principales: Telford, Marco, Navarro, Arcadi, Santpere, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823862/
https://www.ncbi.nlm.nih.gov/pubmed/29472617
http://dx.doi.org/10.1038/s41598-018-21645-x
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author Telford, Marco
Navarro, Arcadi
Santpere, Gabriel
author_facet Telford, Marco
Navarro, Arcadi
Santpere, Gabriel
author_sort Telford, Marco
collection PubMed
description Human herpesviruses 6-A and -B (HHV-6A, HHV-6B) are ubiquitous in human populations worldwide. These viruses have been associated with several diseases such as multiple sclerosis, Hodgkin’s lymphoma or encephalitis. Despite of the need to understand the genetic diversity and geographic stratification of these viruses, the availability of complete viral sequences from different populations is still limited. Here, we present nine new inherited chromosomally integrated HHV-6 sequences from diverse geographical origin which were generated through target DNA enrichment on lymphoblastoid cell lines derived from healthy individuals. Integration with available HHV-6 sequences allowed the assessment of HHV-6A and -6B phylogeny, patterns of recombination and signatures of natural selection. Analysis of the intra-species variability showed differences between A and B diversity levels and revealed that the HHV-6B reference (Z29) is an uncommon sequence, suggesting the need for an alternative reference sequence. Signs of geographical variation are present and more defined in HHV-6A, while they appear partly masked by recombination in HHV-6B. Finally, we conducted a scan for signatures of selection in protein coding genes that yielded at least 6 genes (4 and 2 respectively for the A and B species) showing significant evidence for accelerated evolution, and 1 gene showing evidence of positive selection in HHV-6A.
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spelling pubmed-58238622018-02-26 Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin Telford, Marco Navarro, Arcadi Santpere, Gabriel Sci Rep Article Human herpesviruses 6-A and -B (HHV-6A, HHV-6B) are ubiquitous in human populations worldwide. These viruses have been associated with several diseases such as multiple sclerosis, Hodgkin’s lymphoma or encephalitis. Despite of the need to understand the genetic diversity and geographic stratification of these viruses, the availability of complete viral sequences from different populations is still limited. Here, we present nine new inherited chromosomally integrated HHV-6 sequences from diverse geographical origin which were generated through target DNA enrichment on lymphoblastoid cell lines derived from healthy individuals. Integration with available HHV-6 sequences allowed the assessment of HHV-6A and -6B phylogeny, patterns of recombination and signatures of natural selection. Analysis of the intra-species variability showed differences between A and B diversity levels and revealed that the HHV-6B reference (Z29) is an uncommon sequence, suggesting the need for an alternative reference sequence. Signs of geographical variation are present and more defined in HHV-6A, while they appear partly masked by recombination in HHV-6B. Finally, we conducted a scan for signatures of selection in protein coding genes that yielded at least 6 genes (4 and 2 respectively for the A and B species) showing significant evidence for accelerated evolution, and 1 gene showing evidence of positive selection in HHV-6A. Nature Publishing Group UK 2018-02-22 /pmc/articles/PMC5823862/ /pubmed/29472617 http://dx.doi.org/10.1038/s41598-018-21645-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Telford, Marco
Navarro, Arcadi
Santpere, Gabriel
Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title_full Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title_fullStr Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title_full_unstemmed Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title_short Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin
title_sort whole genome diversity of inherited chromosomally integrated hhv-6 derived from healthy individuals of diverse geographic origin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823862/
https://www.ncbi.nlm.nih.gov/pubmed/29472617
http://dx.doi.org/10.1038/s41598-018-21645-x
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