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Molecular Evolution of Human Adenovirus (HAdV) Species C
Currently, 88 different Human Adenovirus (HAdV) types are grouped into seven HAdV species A to G. Most types (57) belong to species HAdV-D. Recombination between capsid genes (hexon, penton and fiber) is the main factor contributing to the diversity in species HAdV-D. Noteworthy, species HAdV-C cont...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355881/ https://www.ncbi.nlm.nih.gov/pubmed/30705303 http://dx.doi.org/10.1038/s41598-018-37249-4 |
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author | Dhingra, Akshay Hage, Elias Ganzenmueller, Tina Böttcher, Sindy Hofmann, Jörg Hamprecht, Klaus Obermeier, Patrick Rath, Barbara Hausmann, Fabian Dobner, Thomas Heim, Albert |
author_facet | Dhingra, Akshay Hage, Elias Ganzenmueller, Tina Böttcher, Sindy Hofmann, Jörg Hamprecht, Klaus Obermeier, Patrick Rath, Barbara Hausmann, Fabian Dobner, Thomas Heim, Albert |
author_sort | Dhingra, Akshay |
collection | PubMed |
description | Currently, 88 different Human Adenovirus (HAdV) types are grouped into seven HAdV species A to G. Most types (57) belong to species HAdV-D. Recombination between capsid genes (hexon, penton and fiber) is the main factor contributing to the diversity in species HAdV-D. Noteworthy, species HAdV-C contains so far only five types, although species HAdV-C is highly prevalent and clinically significant in immunosuppressed patients. Therefore, the evolution of species HAdV-C was studied by generating 51 complete genome sequences from circulating strains. Clustering of the whole genome HAdV-C sequences confirmed classical typing results (fifteen HAdV-C1, thirty HAdV-C2, four HAdV-C5, two HAdV-C6). However, two HAdV-C2 strains had a novel penton base sequence and thus were re-labeled as the novel type HAdV-C89. Fiber and early gene region 3 (E3) sequences clustered always with the corresponding prototype sequence but clustering of the E4 region indicated recombination events in 26 out of the 51 sequenced specimens. Recombination of the E1 gene region was detected in 16 circulating strains. As early gene region sequences are not considered in the type definition of HAdVs, evolution of HAdV-C remains on the subtype level. Nonetheless, recombination of the E1 and E4 gene regions may influence the virulence of HAdV-C strains. |
format | Online Article Text |
id | pubmed-6355881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63558812019-02-04 Molecular Evolution of Human Adenovirus (HAdV) Species C Dhingra, Akshay Hage, Elias Ganzenmueller, Tina Böttcher, Sindy Hofmann, Jörg Hamprecht, Klaus Obermeier, Patrick Rath, Barbara Hausmann, Fabian Dobner, Thomas Heim, Albert Sci Rep Article Currently, 88 different Human Adenovirus (HAdV) types are grouped into seven HAdV species A to G. Most types (57) belong to species HAdV-D. Recombination between capsid genes (hexon, penton and fiber) is the main factor contributing to the diversity in species HAdV-D. Noteworthy, species HAdV-C contains so far only five types, although species HAdV-C is highly prevalent and clinically significant in immunosuppressed patients. Therefore, the evolution of species HAdV-C was studied by generating 51 complete genome sequences from circulating strains. Clustering of the whole genome HAdV-C sequences confirmed classical typing results (fifteen HAdV-C1, thirty HAdV-C2, four HAdV-C5, two HAdV-C6). However, two HAdV-C2 strains had a novel penton base sequence and thus were re-labeled as the novel type HAdV-C89. Fiber and early gene region 3 (E3) sequences clustered always with the corresponding prototype sequence but clustering of the E4 region indicated recombination events in 26 out of the 51 sequenced specimens. Recombination of the E1 gene region was detected in 16 circulating strains. As early gene region sequences are not considered in the type definition of HAdVs, evolution of HAdV-C remains on the subtype level. Nonetheless, recombination of the E1 and E4 gene regions may influence the virulence of HAdV-C strains. Nature Publishing Group UK 2019-01-31 /pmc/articles/PMC6355881/ /pubmed/30705303 http://dx.doi.org/10.1038/s41598-018-37249-4 Text en © The Author(s) 2019 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 Dhingra, Akshay Hage, Elias Ganzenmueller, Tina Böttcher, Sindy Hofmann, Jörg Hamprecht, Klaus Obermeier, Patrick Rath, Barbara Hausmann, Fabian Dobner, Thomas Heim, Albert Molecular Evolution of Human Adenovirus (HAdV) Species C |
title | Molecular Evolution of Human Adenovirus (HAdV) Species C |
title_full | Molecular Evolution of Human Adenovirus (HAdV) Species C |
title_fullStr | Molecular Evolution of Human Adenovirus (HAdV) Species C |
title_full_unstemmed | Molecular Evolution of Human Adenovirus (HAdV) Species C |
title_short | Molecular Evolution of Human Adenovirus (HAdV) Species C |
title_sort | molecular evolution of human adenovirus (hadv) species c |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355881/ https://www.ncbi.nlm.nih.gov/pubmed/30705303 http://dx.doi.org/10.1038/s41598-018-37249-4 |
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