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Molecular epidemiology of human Borna disease virus 1 infection revisited
Borna disease virus 1 (BoDV-1) strains attracted public interest by recently reported rare fatal encephalitis cases in Germany. Previously, human BoDV-1 infection was suggested to contribute to psychiatric diseases. Clinical outcomes (encephalitis vs. psychiatric disease) and epidemiology (zoonotic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132405/ https://www.ncbi.nlm.nih.gov/pubmed/35437118 http://dx.doi.org/10.1080/22221751.2022.2065931 |
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author | Bode, Liv Guo, Yujie Xie, Peng |
author_facet | Bode, Liv Guo, Yujie Xie, Peng |
author_sort | Bode, Liv |
collection | PubMed |
description | Borna disease virus 1 (BoDV-1) strains attracted public interest by recently reported rare fatal encephalitis cases in Germany. Previously, human BoDV-1 infection was suggested to contribute to psychiatric diseases. Clinical outcomes (encephalitis vs. psychiatric disease) and epidemiology (zoonotic vs. human-to-human transmission) are still controversial. Here, phylogenetic analyses of 18 human and 4 laboratory strains revealed close genomic homologies both in distant geographical regions, and different clinical entities. Single unique amino acid mutations substantiated the authenticity of human strains. No matching was found with those of shrew strains in the same cluster 4, arguing against zoonosis. Opposite epidemiology concepts should be equally considered. |
format | Online Article Text |
id | pubmed-9132405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-91324052022-05-26 Molecular epidemiology of human Borna disease virus 1 infection revisited Bode, Liv Guo, Yujie Xie, Peng Emerg Microbes Infect Article Commentary Borna disease virus 1 (BoDV-1) strains attracted public interest by recently reported rare fatal encephalitis cases in Germany. Previously, human BoDV-1 infection was suggested to contribute to psychiatric diseases. Clinical outcomes (encephalitis vs. psychiatric disease) and epidemiology (zoonotic vs. human-to-human transmission) are still controversial. Here, phylogenetic analyses of 18 human and 4 laboratory strains revealed close genomic homologies both in distant geographical regions, and different clinical entities. Single unique amino acid mutations substantiated the authenticity of human strains. No matching was found with those of shrew strains in the same cluster 4, arguing against zoonosis. Opposite epidemiology concepts should be equally considered. Taylor & Francis 2022-05-23 /pmc/articles/PMC9132405/ /pubmed/35437118 http://dx.doi.org/10.1080/22221751.2022.2065931 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Commentary Bode, Liv Guo, Yujie Xie, Peng Molecular epidemiology of human Borna disease virus 1 infection revisited |
title | Molecular epidemiology of human Borna disease virus 1 infection revisited |
title_full | Molecular epidemiology of human Borna disease virus 1 infection revisited |
title_fullStr | Molecular epidemiology of human Borna disease virus 1 infection revisited |
title_full_unstemmed | Molecular epidemiology of human Borna disease virus 1 infection revisited |
title_short | Molecular epidemiology of human Borna disease virus 1 infection revisited |
title_sort | molecular epidemiology of human borna disease virus 1 infection revisited |
topic | Article Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132405/ https://www.ncbi.nlm.nih.gov/pubmed/35437118 http://dx.doi.org/10.1080/22221751.2022.2065931 |
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