Arana Ainara, Cilla Gustavo, Montes Milagrosa, Gomariz María, Pérez-Trallero Emilio
Servicio de Microbiología, Hospital Universitario Donostia-Instituto de Investigación Biodonostia, San Sebastián, Spain.
Servicio de Microbiología, Hospital Universitario Donostia-Instituto de Investigación Biodonostia, San Sebastián, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), San Sebastián, Spain.
PLoS One. 2014 Jun 3;9(6):e98875. doi: 10.1371/journal.pone.0098875. eCollection 2014.
Noroviruses (NoVs) are genetically diverse, with genogroup II-and within it-genotype 4 (GII.4) being the most prevalent cause of acute gastroenteritis worldwide. The aim of this study was to characterize genogroup II NoV causing acute gastroenteritis in the Basque Country (northern Spain) from 2009-2012.
The presence of NoV RNA was investigated by reverse transcriptase-polymerase chain reaction (RT-PCR) in stool specimens from children younger than 15 years old with community-acquired acute gastroenteritis, and from hospitalized adults or elderly residents of nursing homes with acute gastroenteritis. For genotyping, the open reading frames ORF1 (encoding the polymerase) and ORF2 (encoding the major capsid protein) were partially amplified and sequenced. Recombinant strains were confirmed by PCR of the ORF1/ORF2 junction region.
NoV was detected in 16.0% (453/2826) of acute gastroenteritis episodes in children younger than 2 years, 9.9% (139/1407) in children from 2 to 14 years, and 35.8% (122/341) in adults. Of 317 NoVs characterized, 313 were genogroup II and four were genogroup I. The GII.4 variants Den Haag-2006b and New Orleans-2009 predominated in 2009 and 2010-2011, respectively. In 2012, the New Orleans-2009 variant was partially replaced by the Sydney-2012 variant (GII.Pe/GII.4) and New Orleans-2009/Sydney-2012 recombinant strains. The predominant capsid genotype in all age groups was GII.4, which was the only genotype detected in outbreaks. The second most frequent genotype was GII.3 (including the recently described recombination GII.P16/GII.3), which was detected almost exclusively in children.
Nine different genotypes of NoV genogroup II were detected; among these, intergenotype recombinant strains represented an important part, highlighting the role of recombination in the evolution of NoVs. Detection of new NoV strains, not only GII.4 strains, shortly after their first detection in other parts of the world shows that many NoV strains can spread rapidly.
诺如病毒(NoV)基因多样,其中II基因组及其内的4基因型(GII.4)是全球急性胃肠炎最常见的病因。本研究旨在鉴定2009年至2012年在西班牙北部巴斯克地区引起急性胃肠炎的II基因组NoV的特征。
采用逆转录聚合酶链反应(RT-PCR)检测15岁以下社区获得性急性胃肠炎儿童、住院成人或养老院急性胃肠炎老年居民粪便标本中NoV RNA的存在情况。为进行基因分型,对开放阅读框ORF1(编码聚合酶)和ORF2(编码主要衣壳蛋白)进行部分扩增和测序。通过ORF1/ORF2连接区的PCR确认重组菌株。
在2岁以下儿童的急性胃肠炎发作中,16.0%(453/2826)检测到NoV,2至14岁儿童中为9.9%(139/1407),成人中为35.8%(122/341)。在鉴定的317株NoV中,313株为II基因组,4株为I基因组。GII.4变异株代尔夫特-2006b和新奥尔良-2009分别在2009年和2010 - 2011年占主导地位。2012年,新奥尔良-2009变异株部分被悉尼-2012变异株(GII.Pe/GII.4)和新奥尔良-2009/悉尼-2012重组菌株取代。所有年龄组中主要的衣壳基因型为GII.4,这是暴发中唯一检测到的基因型。第二常见的基因型是GII.3(包括最近描述的重组型GII.P16/GII.3),几乎仅在儿童中检测到。
检测到9种不同的II基因组NoV基因型;其中,基因型间重组菌株占重要部分,突出了重组在NoV进化中的作用。在世界其他地区首次检测到新的NoV菌株后不久,不仅检测到GII.4菌株,这表明许多NoV菌株可迅速传播。