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Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss
Poxviruses are known to evolve slower than RNA viruses with only 1–2 mutations/genome/year. Rather than single mutations, rearrangements such as gene gain and loss, which have been discussed as a possible driver for host adaption, were described in poxviruses. In 2022 and 2023 the world is being cha...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230479/ https://www.ncbi.nlm.nih.gov/pubmed/37256469 http://dx.doi.org/10.1007/s11262-023-02002-1 |
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author | Brinkmann, Annika Kohl, Claudia Pape, Katharina Bourquain, Daniel Thürmer, Andrea Michel, Janine Schaade, Lars Nitsche, Andreas |
author_facet | Brinkmann, Annika Kohl, Claudia Pape, Katharina Bourquain, Daniel Thürmer, Andrea Michel, Janine Schaade, Lars Nitsche, Andreas |
author_sort | Brinkmann, Annika |
collection | PubMed |
description | Poxviruses are known to evolve slower than RNA viruses with only 1–2 mutations/genome/year. Rather than single mutations, rearrangements such as gene gain and loss, which have been discussed as a possible driver for host adaption, were described in poxviruses. In 2022 and 2023 the world is being challenged by the largest global outbreak so far of Mpox virus, and the virus seems to have established itself in the human community for an extended period of time. Here, we report five Mpox virus genomes from Germany with extensive gene duplication and loss, leading to the expansion of the ITR regions from 6400 to up to 24,600 bp. We describe duplications of up to 18,200 bp to the opposed genome end, and deletions at the site of insertion of up to 16,900 bp. Deletions and duplications of genes with functions of supposed immune modulation, virulence and host adaption as B19R, B21R, B22R and D10L are described. In summary, we highlight the need for monitoring rearrangements of the Mpox virus genome rather than for monitoring single mutations only. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11262-023-02002-1. |
format | Online Article Text |
id | pubmed-10230479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102304792023-06-01 Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss Brinkmann, Annika Kohl, Claudia Pape, Katharina Bourquain, Daniel Thürmer, Andrea Michel, Janine Schaade, Lars Nitsche, Andreas Virus Genes Original Paper Poxviruses are known to evolve slower than RNA viruses with only 1–2 mutations/genome/year. Rather than single mutations, rearrangements such as gene gain and loss, which have been discussed as a possible driver for host adaption, were described in poxviruses. In 2022 and 2023 the world is being challenged by the largest global outbreak so far of Mpox virus, and the virus seems to have established itself in the human community for an extended period of time. Here, we report five Mpox virus genomes from Germany with extensive gene duplication and loss, leading to the expansion of the ITR regions from 6400 to up to 24,600 bp. We describe duplications of up to 18,200 bp to the opposed genome end, and deletions at the site of insertion of up to 16,900 bp. Deletions and duplications of genes with functions of supposed immune modulation, virulence and host adaption as B19R, B21R, B22R and D10L are described. In summary, we highlight the need for monitoring rearrangements of the Mpox virus genome rather than for monitoring single mutations only. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11262-023-02002-1. Springer US 2023-05-31 2023 /pmc/articles/PMC10230479/ /pubmed/37256469 http://dx.doi.org/10.1007/s11262-023-02002-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Brinkmann, Annika Kohl, Claudia Pape, Katharina Bourquain, Daniel Thürmer, Andrea Michel, Janine Schaade, Lars Nitsche, Andreas Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title | Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title_full | Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title_fullStr | Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title_full_unstemmed | Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title_short | Extensive ITR expansion of the 2022 Mpox virus genome through gene duplication and gene loss |
title_sort | extensive itr expansion of the 2022 mpox virus genome through gene duplication and gene loss |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230479/ https://www.ncbi.nlm.nih.gov/pubmed/37256469 http://dx.doi.org/10.1007/s11262-023-02002-1 |
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