...
首页> 外文期刊>Virology Journal >Novel norovirus recombinants and GII.4 sub-lineages associated with outbreaks between 2006 and 2010 in Belgium
【24h】

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

机译:2006年至2010年比利时爆发的新型诺如病毒重组体和GII.4子系

获取原文

摘要

Background 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. Results 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. Conclusions 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displaced by the GII.4 2010 subtype, and previously reported epidemic GII.b recombinants seemed to have been superseded by GII.e recombinants in 2009 and GII.g recombinants in 2010.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.
机译:背景诺如病毒(NoVs)是全世界人类急性胃肠炎的重要原因。为了深入了解NoV暴发的流行病学模式并确定在比利时传播的NoVs菌株的遗传变异,我们在2006年12月至2010年12月之间对食源性暴发调查中源自NoVs感染患者的粪便样本进行了分析。在过去的四年中,报告的所有食源性疾病暴发中占11.8%,据报道,在11月中,新病毒暴发的数量呈上升趋势,占2010年所有食源性疾病暴发的30%以上。Genogroup II疾病暴发在很大程度上占主导地位,占所有疾病暴发的90%以上。用63个NoV阳性样品进行了系统发育分析,分析了部分聚合酶(N = 45)和/或衣壳基因(N = 35)的序列。对于12个样品,获得了覆盖ORF1-ORF2连接的序列。在基因组Ⅰ和Ⅱ中发现了多种基因型。 GII.4在重要性上依次为GII.2,GII.7,GII.13,GI.4和GI.7。在研究期间,确定了GII.4 NoVs变体2006a,2006b,2007、2008和2010。此外,系统发育分析还鉴定了不同的重组NoV菌株,这些菌株进一步被表征为基因型(GII.e / GII.4 2007,GII.e / GII.3和GII.g / GII.1)和亚基因型(GII.4 2006b)。 /GII.4 2007和GII.4 2010 / GII.4 2010b)重组子。结论最近4年在比利时流通的NoV通过小规模突变或遗传重组显示出显着的遗传多样性。在此期间,GII.4 2006b被GII.4 2010亚型成功取代,以前报道的流行GII.b重组似乎已被2009年的GII.e重组和2010年的GII.g重组所取代。新型GII.4变体与新型GII重组体的出现可能导致NoV爆发,与2008年和2010年观察到的一样。在这项研究中检测到的重组体中,有两个迄今未报告的菌株GII.e / GII。表征3和GII.g / GII.1。监视对于监视同期传播的菌株以适应预防和治疗策略仍然很重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号