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A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?

A norovirus recombinant GII.P4_NewOrleans_2009/GII.4_Sydney_2012 was first detected in Victoria, Australia, in August 2015 at low frequency, and then re-emerged in June 2016, having undergone genetic changes. Analysis of 14 years’ surveillance data from Victoria suggests a typical delay of two to se...

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Detalles Bibliográficos
Autores principales: Bruggink, Leesa, Catton, Michael, Marshall, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Centre for Disease Prevention and Control (ECDC) 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069427/
https://www.ncbi.nlm.nih.gov/pubmed/27719750
http://dx.doi.org/10.2807/1560-7917.ES.2016.21.39.30353
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author Bruggink, Leesa
Catton, Michael
Marshall, John
author_facet Bruggink, Leesa
Catton, Michael
Marshall, John
author_sort Bruggink, Leesa
collection PubMed
description A norovirus recombinant GII.P4_NewOrleans_2009/GII.4_Sydney_2012 was first detected in Victoria, Australia, in August 2015 at low frequency, and then re-emerged in June 2016, having undergone genetic changes. Analysis of 14 years’ surveillance data from Victoria suggests a typical delay of two to seven months between first detection of a new variant and occurrence of a subsequent epidemic linked to that variant. We consider that the current recombinant strain has the potential to become a pandemic variant.
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spelling pubmed-50694272016-10-21 A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant? Bruggink, Leesa Catton, Michael Marshall, John Euro Surveill Rapid Communication A norovirus recombinant GII.P4_NewOrleans_2009/GII.4_Sydney_2012 was first detected in Victoria, Australia, in August 2015 at low frequency, and then re-emerged in June 2016, having undergone genetic changes. Analysis of 14 years’ surveillance data from Victoria suggests a typical delay of two to seven months between first detection of a new variant and occurrence of a subsequent epidemic linked to that variant. We consider that the current recombinant strain has the potential to become a pandemic variant. European Centre for Disease Prevention and Control (ECDC) 2016-09-29 /pmc/articles/PMC5069427/ /pubmed/27719750 http://dx.doi.org/10.2807/1560-7917.ES.2016.21.39.30353 Text en This article is copyright of ECDC, 2016. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.
spellingShingle Rapid Communication
Bruggink, Leesa
Catton, Michael
Marshall, John
A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title_full A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title_fullStr A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title_full_unstemmed A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title_short A norovirus intervariant GII.4 recombinant in Victoria, Australia, June 2016: the next epidemic variant?
title_sort norovirus intervariant gii.4 recombinant in victoria, australia, june 2016: the next epidemic variant?
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069427/
https://www.ncbi.nlm.nih.gov/pubmed/27719750
http://dx.doi.org/10.2807/1560-7917.ES.2016.21.39.30353
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