NoVs and SaVs exhibited significant genetic diversity in Quebec, with multiple genotypes co-circulating in 2015-2016, including GII.17[P17] and GII.4 Sydney[P31].
The study identifies significant genetic diversity and shifting predominance of Norovirus and Sapovirus genotypes in Quebec outbreaks, including the first detection of several emerging global genotypes.
Absolute Event Rate: 0% vs 0%
Norovirus (NoV) and sapovirus (SaV) are major viral pathogens causing acute gastroenteritis (AGE) in both children and adults in developed countries and are also responsible for large-scale outbreaks. However, in Quebec, Canada, there are limited and updated data with respect to the genotypes circulating and implicated in outbreaks, particularly for SaV. This study aimed to investigate the genetic diversity and genotype predominance of NoVs and SaVs associated with AGE outbreaks in Quebec, Canada. Confirmed NoV and SaV outbreaks from long-term care facilities and hospital settings between September 2011 and April 2016 were investigated (n = 252). NoVs and SaVs were genetically diverse: 21 RdRp-capsid combinations were identified, of which 10 are recombinants. NoV GII.4 New OrleansP4 NewOrleans was the predominant genotype from 2011 to 2013, and GII.4 SydneyP31 was the predominant genotype from 2013 to 2015. In 2015–2016, no single genotype predominated; instead, GII.17P17, GII.4 SydneyP16, GII.4 SydneyP31, and SaV GI.2 strains were co-circulating at similar frequencies. Notably, emerging global genotypes including GII.17P17, GII.4 SydneyP16, GII.2P16, and GII.4 San FranciscoP31 were detected for the first time in Quebec. These findings may contribute to an enhanced understanding of NoV and SaV infection and spread, and to the development of candidate vaccines.
Larocque et al. (Thu,) reported a other. NoVs and SaVs exhibited significant genetic diversity in Quebec, with multiple genotypes co-circulating in 2015-2016, including GII.17[P17] and GII.4 Sydney[P31].
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