Recombinant GII.P16/GII.4 Sydney 2012 Was the Dominant Norovirus Identified in Australia and New Zealand in 2017.
- Publisher:
- MDPI
- Publication Type:
- Journal Article
- Citation:
- Viruses, 2018, 10, (10), pp. E548
- Issue Date:
- 2018-10-09
Open Access
Copyright Clearance Process
- Recently Added
- In Progress
- Open Access
This item is open access.
Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Lun, JH | |
dc.contributor.author | Hewitt, J | |
dc.contributor.author | Yan, GJH | |
dc.contributor.author |
Enosi Tuipulotu, D |
|
dc.contributor.author | Rawlinson, WD | |
dc.contributor.author | White, PA | |
dc.date.accessioned | 2025-01-15T13:44:43Z | |
dc.date.available | 2018-10-06 | |
dc.date.available | 2025-01-15T13:44:43Z | |
dc.date.issued | 2018-10-09 | |
dc.identifier.citation | Viruses, 2018, 10, (10), pp. E548 | |
dc.identifier.issn | 1999-4915 | |
dc.identifier.issn | 1999-4915 | |
dc.identifier.uri | http://hdl.handle.net/10453/183662 | |
dc.description.abstract | For the past two decades, norovirus pandemic variants have emerged every 3⁻5 years, and dominate until they are replaced by alternate strains. However, this scenario changed in 2016 with the co-circulation of six prevalent viruses, three of which possessed the pandemic GII.4 Sydney 2012 capsid. An increased number of institutional gastroenteritis outbreaks were reported within the Oceania region in mid-2017. This study identified emerging noroviruses circulating in Australia and New Zealand in 2017 to assess the changing dynamics of the virus infection. RT-PCR-based methods, next generation sequencing, and phylogenetic analyses were used to genotype noroviruses from both clinical and wastewater samples. Antigenic changes were observed between the capsid of pandemic Sydney 2012 variant and the two new Sydney recombinant viruses. The combination of these antigenic changes and the acquisition of a new ORF1 through recombination could both facilitate their ongoing persistence in the population. Overall, an increased prevalence of GII.P16/GII.4 Sydney 2012 viruses was observed in 2017, replacing the GII.P16/GII.2 recombinant that dominated in the region at the end of 2016. This shift in strain dominance was also observed in wastewater samples, demonstrating the reliability of wastewater as a molecular surveillance tool. | |
dc.format | Electronic | |
dc.language | eng | |
dc.publisher | MDPI | |
dc.relation.ispartof | Viruses | |
dc.relation.isbasedon | 10.3390/v10100548 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0605 Microbiology | |
dc.subject.classification | 3107 Microbiology | |
dc.subject.mesh | Australia | |
dc.subject.mesh | Capsid Proteins | |
dc.subject.mesh | Gastroenteritis | |
dc.subject.mesh | Genotype | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Molecular Epidemiology | |
dc.subject.mesh | New Zealand | |
dc.subject.mesh | Norovirus | |
dc.subject.mesh | Open Reading Frames | |
dc.subject.mesh | Phylogeny | |
dc.subject.mesh | Recombination, Genetic | |
dc.subject.mesh | Wastewater | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Norovirus | |
dc.subject.mesh | Gastroenteritis | |
dc.subject.mesh | Capsid Proteins | |
dc.subject.mesh | Phylogeny | |
dc.subject.mesh | Recombination, Genetic | |
dc.subject.mesh | Genotype | |
dc.subject.mesh | Open Reading Frames | |
dc.subject.mesh | Australia | |
dc.subject.mesh | New Zealand | |
dc.subject.mesh | Molecular Epidemiology | |
dc.subject.mesh | Wastewater | |
dc.subject.mesh | Australia | |
dc.subject.mesh | Capsid Proteins | |
dc.subject.mesh | Gastroenteritis | |
dc.subject.mesh | Genotype | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Molecular Epidemiology | |
dc.subject.mesh | New Zealand | |
dc.subject.mesh | Norovirus | |
dc.subject.mesh | Open Reading Frames | |
dc.subject.mesh | Phylogeny | |
dc.subject.mesh | Recombination, Genetic | |
dc.subject.mesh | Wastewater | |
dc.title | Recombinant GII.P16/GII.4 Sydney 2012 Was the Dominant Norovirus Identified in Australia and New Zealand in 2017. | |
dc.type | Journal Article | |
utslib.citation.volume | 10 | |
utslib.location.activity | Switzerland | |
utslib.for | 0605 Microbiology | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science/School of Life Sciences | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2025-01-15T13:44:42Z | |
pubs.issue | 10 | |
pubs.publication-status | Published online | |
pubs.volume | 10 | |
utslib.citation.issue | 10 |
Abstract:
For the past two decades, norovirus pandemic variants have emerged every 3⁻5 years, and dominate until they are replaced by alternate strains. However, this scenario changed in 2016 with the co-circulation of six prevalent viruses, three of which possessed the pandemic GII.4 Sydney 2012 capsid. An increased number of institutional gastroenteritis outbreaks were reported within the Oceania region in mid-2017. This study identified emerging noroviruses circulating in Australia and New Zealand in 2017 to assess the changing dynamics of the virus infection. RT-PCR-based methods, next generation sequencing, and phylogenetic analyses were used to genotype noroviruses from both clinical and wastewater samples. Antigenic changes were observed between the capsid of pandemic Sydney 2012 variant and the two new Sydney recombinant viruses. The combination of these antigenic changes and the acquisition of a new ORF1 through recombination could both facilitate their ongoing persistence in the population. Overall, an increased prevalence of GII.P16/GII.4 Sydney 2012 viruses was observed in 2017, replacing the GII.P16/GII.2 recombinant that dominated in the region at the end of 2016. This shift in strain dominance was also observed in wastewater samples, demonstrating the reliability of wastewater as a molecular surveillance tool.
Please use this identifier to cite or link to this item:
Download statistics for the last 12 months
Not enough data to produce graph