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Novel Approach for Detection of Enteric Viruses To Enable Syndrome Surveillance of Acute Viral Gastroenteritis

机译:检测肠病毒以实现对急性病毒性胃肠炎的综合征监测的新方法

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Acute gastroenteritis is one of the most common diseases worldwide, with viruses, particularly noroviruses, being the leading cause in developed countries. In The Netherlands, systematic surveillance of gastroenteritis outbreaks of suspected viral etiology was established by the National Institute for Public Health and the Environment in 1994. Since 2002, the total number of outbreaks reported has been increasing, and with that comes the need for sensitive assays that can be performed quickly. In addition, the diagnostic demand changed so that now the proportion of samples from hospitals is higher and there is a need for patient-based test results. In order to target the diagnosis of acute gastroenteritis, we reviewed our data on outbreaks of gastroenteritis and the prevalence of individual viruses to provide a priority list of viruses for which samples should be evaluated. Random primers were used to replace the separate specific primers for each virus used in the reverse transcription steps. The individual PCR assays were replaced by multiplex PCR assays. We employed a two-step method in which in the first step we screened for the most common causes of viral gastroenteritis, noroviruses of genogroup II and rotaviruses of group A, with equine arteritis virus used as the internal control. Subsequently, in the second step, two parallel PCR assays were developed for the detection of noroviruses of genogroup I and equine arteritis virus in one run and adenoviruses, sapoviruses, and astroviruses in the other run. The specificities of the assays were calculated to be 92.5% for the assay for noroviruses of genogroup I and 100% for the assays for all other viruses, the detection limits were equal for all viruses, and the turnaround time was reduced to 1 day compared to the at least 3 days required for the methods used previously. This approach allows the targeted, rapid, and cost-effective elucidation of the causes of acute gastroenteritis outbreaks.
机译:急性肠胃炎是全世界最常见的疾病之一,病毒,特别是诺如病毒,是发达国家的主要原因。在荷兰,国家公共卫生与环境研究所于1994年建立了对可疑病毒病因的胃肠炎暴发的系统监测。自2002年以来,报告的暴发总数一直在增加,因此需要灵敏的检测方法可以快速执行。另外,诊断需求发生了变化,因此现在医院中的样本比例更高,并且需要基于患者的测试结果。为了针对急性胃肠炎的诊断,我们回顾了有关胃肠炎暴发和个别病毒的流行情况的数据,以提供应评估样本的病毒的优先列表。对于逆转录步骤中使用的每种病毒,使用随机引物代替单独的特异性引物。单独的PCR分析被多重PCR分析取代。我们采用了两步法,在第一步中,我们以马动脉炎病毒作为内部对照,筛选出病毒性肠胃炎,基因组II的诺如病毒和A组轮状病毒的最常见原因。随后,在第二步中,开发了两个并行的PCR检测方法,用于一次检测基因组I的诺如病毒和马动脉炎病毒,而另一次检测腺病毒,沙波病毒和星状病毒。计算得出的基因组I诺如病毒的检测特异性为92.5%,所有其他病毒的检测特异性为100%,所有病毒的检出限均相等,与之相比,周转时间减少至1天之前使用的方法至少需要3天。这种方法可以针对性,快速且经济高效地阐明急性胃肠炎暴发的原因。

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