Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium

<p>Abstract</p> <p>Background</p> <p>Noroviruses (NoVs) are an important cause of acute gastroenteritis in humans worldwide. To gain insight into the epidemiologic patterns of NoV outbreaks and to determine the genetic variation of NoVs strains circulating in Belgium, s...

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Main Authors: Vanderplasschen Alain, Scipioni Alexandra, Botteldoorn Nadine, Palmeira Leonor, Denayer Sarah, Mathijs Elisabeth, Thiry Etienne, Dierick Katelijne
Format: Article
Language:English
Published: BMC 2011-06-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/8/1/310
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spelling doaj-b49bcfc0643d4fa4906cc179fbb887f72020-11-25T02:33:35ZengBMCVirology Journal1743-422X2011-06-018131010.1186/1743-422X-8-310Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in BelgiumVanderplasschen AlainScipioni AlexandraBotteldoorn NadinePalmeira LeonorDenayer SarahMathijs ElisabethThiry EtienneDierick Katelijne<p>Abstract</p> <p>Background</p> <p>Noroviruses (NoVs) are an important cause of acute gastroenteritis in humans worldwide. To gain insight into the epidemiologic patterns of NoV outbreaks and to determine the genetic variation of NoVs strains circulating in Belgium, stool samples originating from patients infected with NoVs in foodborne outbreak investigations were analysed between December 2006 and December 2010.</p> <p>Results</p> <p>NoVs were found responsible of 11.8% of all suspected foodborne outbreaks reported in the last 4 years and the number of NoV outbreaks reported increased along the years representing more than 30% of all foodborne outbreaks in 2010. Genogroup II outbreaks largely predominated and represented more than 90% of all outbreaks. Phylogenetic analyses were performed with 63 NoV-positive samples for the partial polymerase (N = 45) and/or capsid gene (N = 35) sequences. For 12 samples, sequences covering the ORF1-ORF2 junction were obtained. A variety of genotypes was found among genogroups I and II; GII.4 was predominant followed in order of importance by GII.2, GII.7, GII.13, GI.4 and GI.7. In the study period, GII.4 NoVs variants 2006a, 2006b, 2007, 2008 and 2010 were identified. Moreover, phylogenetic analyses identified different recombinant NoV strains that were further characterised as intergenotype (GII.e/GII.4 2007, GII.e/GII.3 and GII.g/GII.1) and intersub-genotype (GII.4 2006b/GII.4 2007 and GII.4 2010/GII.4 2010b) recombinants.</p> <p>Conclusions</p> <p>NoVs circulating in the last 4 years in Belgium showed remarkable genetic diversity either by small-scale mutations or genetic recombination. In this period, GII.4 2006b was successfully displaced by the GII.4 2010 subtype, and previously reported epidemic GII.b recombinants seemed to have been superseded by GII.e recombinants in 2009 and GII.g recombinants in 2010. This study showed that the emergence of novel GII.4 variants together with novel GII recombinants could lead to an explosion in NoV outbreaks, likewise to what was observed in 2008 and 2010. Among recombinants detected in this study, two hitherto unreported strains GII.e/GII.3 and GII.g/GII.1 were characterised. Surveillance will remain important to monitor contemporaneously circulating strains in order to adapt preventive and curative strategies.</p> http://www.virologyj.com/content/8/1/310
collection DOAJ
language English
format Article
sources DOAJ
author Vanderplasschen Alain
Scipioni Alexandra
Botteldoorn Nadine
Palmeira Leonor
Denayer Sarah
Mathijs Elisabeth
Thiry Etienne
Dierick Katelijne
spellingShingle Vanderplasschen Alain
Scipioni Alexandra
Botteldoorn Nadine
Palmeira Leonor
Denayer Sarah
Mathijs Elisabeth
Thiry Etienne
Dierick Katelijne
Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
Virology Journal
author_facet Vanderplasschen Alain
Scipioni Alexandra
Botteldoorn Nadine
Palmeira Leonor
Denayer Sarah
Mathijs Elisabeth
Thiry Etienne
Dierick Katelijne
author_sort Vanderplasschen Alain
title Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
title_short Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
title_full Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
title_fullStr Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
title_full_unstemmed Novel norovirus recombinants and of GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
title_sort novel norovirus recombinants and of gii.4 sub-lineages associated with outbreaks between 2006 and 2010 in belgium
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-06-01
description <p>Abstract</p> <p>Background</p> <p>Noroviruses (NoVs) are an important cause of acute gastroenteritis in humans worldwide. To gain insight into the epidemiologic patterns of NoV outbreaks and to determine the genetic variation of NoVs strains circulating in Belgium, stool samples originating from patients infected with NoVs in foodborne outbreak investigations were analysed between December 2006 and December 2010.</p> <p>Results</p> <p>NoVs were found responsible of 11.8% of all suspected foodborne outbreaks reported in the last 4 years and the number of NoV outbreaks reported increased along the years representing more than 30% of all foodborne outbreaks in 2010. Genogroup II outbreaks largely predominated and represented more than 90% of all outbreaks. Phylogenetic analyses were performed with 63 NoV-positive samples for the partial polymerase (N = 45) and/or capsid gene (N = 35) sequences. For 12 samples, sequences covering the ORF1-ORF2 junction were obtained. A variety of genotypes was found among genogroups I and II; GII.4 was predominant followed in order of importance by GII.2, GII.7, GII.13, GI.4 and GI.7. In the study period, GII.4 NoVs variants 2006a, 2006b, 2007, 2008 and 2010 were identified. Moreover, phylogenetic analyses identified different recombinant NoV strains that were further characterised as intergenotype (GII.e/GII.4 2007, GII.e/GII.3 and GII.g/GII.1) and intersub-genotype (GII.4 2006b/GII.4 2007 and GII.4 2010/GII.4 2010b) recombinants.</p> <p>Conclusions</p> <p>NoVs circulating in the last 4 years in Belgium showed remarkable genetic diversity either by small-scale mutations or genetic recombination. In this period, GII.4 2006b was successfully displaced by the GII.4 2010 subtype, and previously reported epidemic GII.b recombinants seemed to have been superseded by GII.e recombinants in 2009 and GII.g recombinants in 2010. This study showed that the emergence of novel GII.4 variants together with novel GII recombinants could lead to an explosion in NoV outbreaks, likewise to what was observed in 2008 and 2010. Among recombinants detected in this study, two hitherto unreported strains GII.e/GII.3 and GII.g/GII.1 were characterised. Surveillance will remain important to monitor contemporaneously circulating strains in order to adapt preventive and curative strategies.</p>
url http://www.virologyj.com/content/8/1/310
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