Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample
Abstract We recovered the first full-length poxvirus genome, including the terminal hairpin region, directly from complex clinical material using a combination of second generation short read and third generation nanopore sequencing technologies. The complete viral genome sequence was directly recov...
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Nature Portfolio
2017
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oai:doaj.org-article:756dc6fd915c4b93802783d41f08e1ca2021-12-02T16:06:50ZRecovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample10.1038/s41598-017-03997-y2045-2322https://doaj.org/article/756dc6fd915c4b93802783d41f08e1ca2017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03997-yhttps://doaj.org/toc/2045-2322Abstract We recovered the first full-length poxvirus genome, including the terminal hairpin region, directly from complex clinical material using a combination of second generation short read and third generation nanopore sequencing technologies. The complete viral genome sequence was directly recovered from a skin lesion of a grey seal thereby preventing sequence changes due to in vitro passaging of the virus. Subsequent analysis of the proteins encoded by this virus identified genes specific for skin adaptation and pathogenesis of parapoxviruses. These data warrant the classification of seal parapoxvirus, tentatively designated SePPV, as a new species within the genus Parapoxvirus.Thomas GüntherLudwig HaasMalik AlawiPeter WohlseinJerzy MarksAdam GrundhoffPaul BecherNicole FischerNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-8 (2017) |
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Medicine R Science Q Thomas Günther Ludwig Haas Malik Alawi Peter Wohlsein Jerzy Marks Adam Grundhoff Paul Becher Nicole Fischer Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
description |
Abstract We recovered the first full-length poxvirus genome, including the terminal hairpin region, directly from complex clinical material using a combination of second generation short read and third generation nanopore sequencing technologies. The complete viral genome sequence was directly recovered from a skin lesion of a grey seal thereby preventing sequence changes due to in vitro passaging of the virus. Subsequent analysis of the proteins encoded by this virus identified genes specific for skin adaptation and pathogenesis of parapoxviruses. These data warrant the classification of seal parapoxvirus, tentatively designated SePPV, as a new species within the genus Parapoxvirus. |
format |
article |
author |
Thomas Günther Ludwig Haas Malik Alawi Peter Wohlsein Jerzy Marks Adam Grundhoff Paul Becher Nicole Fischer |
author_facet |
Thomas Günther Ludwig Haas Malik Alawi Peter Wohlsein Jerzy Marks Adam Grundhoff Paul Becher Nicole Fischer |
author_sort |
Thomas Günther |
title |
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
title_short |
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
title_full |
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
title_fullStr |
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
title_full_unstemmed |
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
title_sort |
recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sample |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/756dc6fd915c4b93802783d41f08e1ca |
work_keys_str_mv |
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1718384849129046016 |