首页> 外文期刊>Revista de Patologia Tropical >SCREENING OF FECAL SAMPLES FROM ASYMPTOMATIC CHILDREN, FOR NOROVIRUS DETECTION, USING A THIRD GENERATION ENZYME IMMUNOASSAY COMMERCIAL KIT
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SCREENING OF FECAL SAMPLES FROM ASYMPTOMATIC CHILDREN, FOR NOROVIRUS DETECTION, USING A THIRD GENERATION ENZYME IMMUNOASSAY COMMERCIAL KIT

机译:使用第三代酶免疫分析商业试剂盒从无症状儿童的粪便样本中筛查诺如病毒

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Norovirus is the leading cause of non-bacterial acute gastroenteritis outbreaks worldwide. Recently, third generation Enzyme Immunoassay (EIA) commercial kits have been developed, and controversial results have been obtained by different studies regarding the sensitivity and specificity of these assays. Therefore, the aim of this study was to test 60 fecal samples, previously tested as positive by RT-PCR for caliciviruses (40 norovirus-positive and 20 sapovirus-positive samples), for qualitative determination of genogroup I and II noroviruses by a commercial EIA kit (RIDASCREEN? Norovirus (C1401) 3rd Generation, R-Biopharm, Darmstadt, Germany). The samples were obtained from 30 children aged less than five years, mostly asymptomatic, who attend a day-care center in Goiania, Goiás, Brazil. The results conferred a positivity rate for NoV of 35% and a specificity rate of 100% for the EIA, when compared to the RT-PCR. The test also failed to detect samples that were positive for GI.1 and GI.4 norovirus. The presumably lower viral load of asymptomatic children might be related to the poor sensitivity. Our results reinforce the notion thatscreening of samples by molecular assays, especially of samples that might have a low number of viral particles such as those obtained from asymptomatic patients, should not be replaced by the use of EIA kits.
机译:诺如病毒是全球非细菌性急性胃肠炎暴发的主要原因。近来,已经开发了第三代酶免疫测定(EIA)商业试剂盒,并且关于这些测定的灵敏度和特异性的不同研究已经获得了有争议的结果。因此,本研究的目的是测试60份粪便样品,这些样品先前已通过RT-PCR对杯状病毒进行了阳性检测(40株诺如病毒阳性和20例甲状旁腺病毒阳性样品),以通过商业EIA定性确定基因组I和II诺如病毒。试剂盒(RIDASCREEN?Norovirus(C1401)第三代,R-Biopharm,德国达姆施塔特)。样本取自30名不到5岁的儿童,大多数没有症状,他们在巴西戈亚斯州戈亚尼亚的一家日托中心就读。与RT-PCR相比,结果显示NoV的阳性率为35%,EIA的特异性率为100%。该测试也未能检测出GI.1和GI.4诺如病毒呈阳性的样品。无症状儿童的病毒载量可能较低,可能与敏感性差有关。我们的结果强化了这样的观念,即通过分子测定来筛查样品,尤其是可能含有少量病毒颗粒的样品(例如从无症状患者那里获得的样品),不应使用EIA试剂盒来代替。

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