Cargando…

The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission

Noroviruses are a leading cause of human gastroenteritis worldwide. The norovirus genotype GII.4 is the most prevalent genotype in the human population and has caused six pandemics since 1995. A novel norovirus lineage containing the GII.P16 polymerase and pandemic GII.4 Sydney 2012 capsid was recen...

Descripción completa

Detalles Bibliográficos
Autores principales: Ruis, Christopher, Roy, Sunando, Brown, Julianne R., Allen, David J., Goldstein, Richard A., Breuer, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491022/
https://www.ncbi.nlm.nih.gov/pubmed/28662035
http://dx.doi.org/10.1371/journal.pone.0179572
_version_ 1783247064843419648
author Ruis, Christopher
Roy, Sunando
Brown, Julianne R.
Allen, David J.
Goldstein, Richard A.
Breuer, Judith
author_facet Ruis, Christopher
Roy, Sunando
Brown, Julianne R.
Allen, David J.
Goldstein, Richard A.
Breuer, Judith
author_sort Ruis, Christopher
collection PubMed
description Noroviruses are a leading cause of human gastroenteritis worldwide. The norovirus genotype GII.4 is the most prevalent genotype in the human population and has caused six pandemics since 1995. A novel norovirus lineage containing the GII.P16 polymerase and pandemic GII.4 Sydney 2012 capsid was recently detected in Asia and Germany. We demonstrate that this lineage is also circulating within the UK and USA and has been circulating since October 2014 or earlier. While the lineage does not contain unique substitutions in the capsid, it does contain polymerase substitutions close to positions known to influence polymerase function and virus transmission. These polymerase substitutions are shared with a GII.P16-GII.2 virus that dominated outbreaks in Germany in Winter 2016. We suggest that the substitutions in the polymerase may have resulted in a more transmissible virus and the combination of this polymerase and the pandemic GII.4 capsid may result in a highly transmissible virus. Further surveillance efforts will be required to determine whether the GII.P16-GII.4 Sydney 2012 lineage increases in frequency over the coming months.
format Online
Article
Text
id pubmed-5491022
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-54910222017-07-18 The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission Ruis, Christopher Roy, Sunando Brown, Julianne R. Allen, David J. Goldstein, Richard A. Breuer, Judith PLoS One Research Article Noroviruses are a leading cause of human gastroenteritis worldwide. The norovirus genotype GII.4 is the most prevalent genotype in the human population and has caused six pandemics since 1995. A novel norovirus lineage containing the GII.P16 polymerase and pandemic GII.4 Sydney 2012 capsid was recently detected in Asia and Germany. We demonstrate that this lineage is also circulating within the UK and USA and has been circulating since October 2014 or earlier. While the lineage does not contain unique substitutions in the capsid, it does contain polymerase substitutions close to positions known to influence polymerase function and virus transmission. These polymerase substitutions are shared with a GII.P16-GII.2 virus that dominated outbreaks in Germany in Winter 2016. We suggest that the substitutions in the polymerase may have resulted in a more transmissible virus and the combination of this polymerase and the pandemic GII.4 capsid may result in a highly transmissible virus. Further surveillance efforts will be required to determine whether the GII.P16-GII.4 Sydney 2012 lineage increases in frequency over the coming months. Public Library of Science 2017-06-29 /pmc/articles/PMC5491022/ /pubmed/28662035 http://dx.doi.org/10.1371/journal.pone.0179572 Text en © 2017 Ruis et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ruis, Christopher
Roy, Sunando
Brown, Julianne R.
Allen, David J.
Goldstein, Richard A.
Breuer, Judith
The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title_full The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title_fullStr The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title_full_unstemmed The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title_short The emerging GII.P16-GII.4 Sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
title_sort emerging gii.p16-gii.4 sydney 2012 norovirus lineage is circulating worldwide, arose by late-2014 and contains polymerase changes that may increase virus transmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491022/
https://www.ncbi.nlm.nih.gov/pubmed/28662035
http://dx.doi.org/10.1371/journal.pone.0179572
work_keys_str_mv AT ruischristopher theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT roysunando theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT brownjulianner theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT allendavidj theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT goldsteinricharda theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT breuerjudith theemerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT ruischristopher emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT roysunando emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT brownjulianner emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT allendavidj emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT goldsteinricharda emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission
AT breuerjudith emerginggiip16gii4sydney2012noroviruslineageiscirculatingworldwidearosebylate2014andcontainspolymerasechangesthatmayincreasevirustransmission