Department of Infectious and Parasitic Diseases, Veterinary Virology and Animal Viral Diseases, Faculty of Veterinary Medicine, University of Liege, Liege, Belgium.
Virol J. 2011 Jun 18;8:310. doi: 10.1186/1743-422X-8-310.
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.
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.
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displaced by the GII.4 2010 subtype, and previously reported epidemic GII.b recombinants seemed to have been superseded by GII.e recombinants in 2009 and GII.g recombinants in 2010.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.
诺如病毒(NoV)是全球人类急性肠胃炎的重要病因。为了深入了解诺如病毒爆发的流行模式,并确定在比利时流行的诺如病毒株的遗传变异情况,对 2006 年 12 月至 2010 年 12 月期间,在食源性暴发调查中感染诺如病毒的患者粪便样本进行了分析。
诺如病毒占过去 4 年报告的所有疑似食源性暴发的 11.8%,且报告的诺如病毒暴发数量逐年增加,占 2010 年所有食源性暴发的 30%以上。基因 II 组暴发占绝对优势,占所有暴发的 90%以上。对 63 份诺如病毒阳性样本进行了部分聚合酶(N=45)和/或衣壳基因(N=35)序列的系统进化分析。对 12 个样本获得了覆盖 ORF1-ORF2 连接区的序列。在基因 I 和 II 组中发现了多种基因型;其次是 GII.4,其次是 GII.2、GII.7、GII.13、GI.4 和 GI.7。在研究期间,鉴定出了 2006a、2006b、2007、2008 和 2010 年的 GII.4 NoV 变异体。此外,系统进化分析还鉴定出了不同的重组诺如病毒株,进一步鉴定为基因型间(GII.e/GII.4 2007、GII.e/GII.3 和 GII.g/GII.1)和亚基因型间(GII.4 2006b/GII.4 2007 和 GII.4 2010/GII.4 2010b)重组体。
在过去的 4 年中,在比利时流行的诺如病毒显示出显著的遗传多样性,无论是通过小规模突变还是遗传重组。在此期间,GII.4 2006b 被 GII.4 2010 亚型成功取代,此前报道的流行 GII.b 重组体似乎在 2009 年被 GII.e 重组体取代,在 2010 年被 GII.g 重组体取代。本研究表明,新型 GII.4 变异体和新型 GII 重组体的出现可能导致诺如病毒暴发的爆发,就像 2008 年和 2010 年所观察到的那样。在本研究中检测到的重组体中,有两种迄今未报道的菌株 GII.e/GII.3 和 GII.g/GII.1。为了适应预防和治疗策略,监测同时流行的菌株仍然很重要。