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Probing the Viromic Frontiers

Modern molecular technology, and particularly high-throughput sequencing (HTS), has revolutionized virus discovery and expanded the depth and breadth of the virome. Recent HTS was used to identify and discover a previously undescribed member of the family Flaviviridae that has genomic features chara...

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Autor principal: Rasmussen, Angela L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659475/
https://www.ncbi.nlm.nih.gov/pubmed/26556279
http://dx.doi.org/10.1128/mBio.01767-15
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author Rasmussen, Angela L.
author_facet Rasmussen, Angela L.
author_sort Rasmussen, Angela L.
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description Modern molecular technology, and particularly high-throughput sequencing (HTS), has revolutionized virus discovery and expanded the depth and breadth of the virome. Recent HTS was used to identify and discover a previously undescribed member of the family Flaviviridae that has genomic features characteristic of both hepaciviruses and pegiviruses. This virus, designated human hepegivirus-1 (HHpgV-1), may represent a previously undescribed new genus in the Flaviviridae family with implications for public health and blood supply safety. Detecting uncharacterized viruses such as HHpgV-1 in clinical samples requires an unbiased screening method that is as sensitive as PCR, while simultaneously detecting multiple rare viral sequences. The virome-capture-sequencing platform for vertebrate viruses (VirCapSeq-VERT) uses positive-selection oligonucleotide capture to sensitively detect sequences from every known vertebrate virus, even in high-background specimens with low-abundance viruses. VirCapSeq-VERT can also detect uncharacterized viruses with sequence homology to known viruses, enabling a new paradigm for virus detection.
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spelling pubmed-46594752015-12-02 Probing the Viromic Frontiers Rasmussen, Angela L. mBio Commentary Modern molecular technology, and particularly high-throughput sequencing (HTS), has revolutionized virus discovery and expanded the depth and breadth of the virome. Recent HTS was used to identify and discover a previously undescribed member of the family Flaviviridae that has genomic features characteristic of both hepaciviruses and pegiviruses. This virus, designated human hepegivirus-1 (HHpgV-1), may represent a previously undescribed new genus in the Flaviviridae family with implications for public health and blood supply safety. Detecting uncharacterized viruses such as HHpgV-1 in clinical samples requires an unbiased screening method that is as sensitive as PCR, while simultaneously detecting multiple rare viral sequences. The virome-capture-sequencing platform for vertebrate viruses (VirCapSeq-VERT) uses positive-selection oligonucleotide capture to sensitively detect sequences from every known vertebrate virus, even in high-background specimens with low-abundance viruses. VirCapSeq-VERT can also detect uncharacterized viruses with sequence homology to known viruses, enabling a new paradigm for virus detection. American Society of Microbiology 2015-11-10 /pmc/articles/PMC4659475/ /pubmed/26556279 http://dx.doi.org/10.1128/mBio.01767-15 Text en Copyright © 2015 Rasmussen. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Commentary
Rasmussen, Angela L.
Probing the Viromic Frontiers
title Probing the Viromic Frontiers
title_full Probing the Viromic Frontiers
title_fullStr Probing the Viromic Frontiers
title_full_unstemmed Probing the Viromic Frontiers
title_short Probing the Viromic Frontiers
title_sort probing the viromic frontiers
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659475/
https://www.ncbi.nlm.nih.gov/pubmed/26556279
http://dx.doi.org/10.1128/mBio.01767-15
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