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Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3

In this study, two human bocaviruses (HBoV), HBoV2 and HBoV3, that were detected previously in enteric samples were characterized genetically. Nearly complete genome sequences of three HBoV2 variants and one HBoV3 variant originating from Thailand and the UK were compared to published HBoV sequences...

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Detalles Bibliográficos
Autores principales: Chieochansin, Thaweesak, Simmonds, Peter, Poovorawan, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086703/
https://www.ncbi.nlm.nih.gov/pubmed/20686798
http://dx.doi.org/10.1007/s00705-010-0781-2
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author Chieochansin, Thaweesak
Simmonds, Peter
Poovorawan, Yong
author_facet Chieochansin, Thaweesak
Simmonds, Peter
Poovorawan, Yong
author_sort Chieochansin, Thaweesak
collection PubMed
description In this study, two human bocaviruses (HBoV), HBoV2 and HBoV3, that were detected previously in enteric samples were characterized genetically. Nearly complete genome sequences of three HBoV2 variants and one HBoV3 variant originating from Thailand and the UK were compared to published HBoV sequences. HBoV2 showed divergence from HBoV1 throughout the genome, while the HBoV3 sequence grouped phylogenetically with HBoV1 in the non-structural region and with HBoV2 sequences in the structural gene, consistent with its proposed recombinant origin. Compared to HBoV1 and HBoV3, HBoV2 shows substantially greater intra-species diversity, consistent with a longer period of human circulation.
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spelling pubmed-70867032020-03-23 Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3 Chieochansin, Thaweesak Simmonds, Peter Poovorawan, Yong Arch Virol Brief Report In this study, two human bocaviruses (HBoV), HBoV2 and HBoV3, that were detected previously in enteric samples were characterized genetically. Nearly complete genome sequences of three HBoV2 variants and one HBoV3 variant originating from Thailand and the UK were compared to published HBoV sequences. HBoV2 showed divergence from HBoV1 throughout the genome, while the HBoV3 sequence grouped phylogenetically with HBoV1 in the non-structural region and with HBoV2 sequences in the structural gene, consistent with its proposed recombinant origin. Compared to HBoV1 and HBoV3, HBoV2 shows substantially greater intra-species diversity, consistent with a longer period of human circulation. Springer Vienna 2010-08-05 2010 /pmc/articles/PMC7086703/ /pubmed/20686798 http://dx.doi.org/10.1007/s00705-010-0781-2 Text en © Springer-Verlag 2010 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Brief Report
Chieochansin, Thaweesak
Simmonds, Peter
Poovorawan, Yong
Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title_full Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title_fullStr Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title_full_unstemmed Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title_short Determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
title_sort determination and analysis of complete coding sequence regions of new discovered human bocavirus types 2 and 3
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086703/
https://www.ncbi.nlm.nih.gov/pubmed/20686798
http://dx.doi.org/10.1007/s00705-010-0781-2
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