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诺如病毒胃肠炎诊断的快速免疫层析试验评估。

Assessment of a rapid immunochromatographic test for the diagnosis of norovirus gastroenteritis.

机构信息

Department of Microbiology, Faculty of Public Health, Mahidol University, 420/1 Ratchawithi Road, Bangkok, 10400, Thailand.

出版信息

Eur J Clin Microbiol Infect Dis. 2012 Sep;31(9):2379-83. doi: 10.1007/s10096-012-1579-9. Epub 2012 Feb 23.

DOI:10.1007/s10096-012-1579-9
PMID:22354525
Abstract

Noroviruses are the leading cause of acute gastroenteritis in people of all ages. Since the viruses are highly infectious, rapid and early diagnosis is important to prevent and control the disease. The present study aimed to evaluate the commercial immunochromatographic test RIDA® QUICK Norovirus for the detection of norovirus in stool samples from patients with acute gastroenteritis in Thailand. As compared with reference RT-PCR results, the RIDA® QUICK Norovirus assay provided a sensitivity of 48.2 and 83.3% with a specificity of 87.5%. False positive results were observed in 12.5% of norovirus-negative stool samples. Based on commercial quantitative real-time RT-PCR, the RIDA® QUICK Norovirus assay revealed a highly significant association, p-value <0.001, and good agreement (kappa = 0.6). The assay could detect norovirus in stool samples ranging from 3.22 × 10(6) to 3.26 × 10(8) copies/ml. False negative results occurred in the stool samples containing 5.9 × 10(6) copies/ml of norovirus GI or 1.85 × 10(4) - 4.28 × 10(5) copies/ml of GII. The immunochromatographic RIDA® QUICK Norovirus assay may be useful for rapid screening of norovirus infections in patients with acute gastroenteritis in both developed and developing countries where the RT-PCR method has not been established for routine diagnosis.

摘要

诺如病毒是各年龄段人群急性肠胃炎的主要病因。由于这些病毒具有高度传染性,因此快速、早期诊断对于预防和控制疾病非常重要。本研究旨在评估 RIDA® QUICK 诺如病毒免疫层析检测法用于检测泰国急性肠胃炎患者粪便样本中的诺如病毒。与参考 RT-PCR 结果相比,RIDA® QUICK 诺如病毒检测法的灵敏度分别为 48.2%和 83.3%,特异性为 87.5%。在 12.5%的诺如病毒阴性粪便样本中观察到假阳性结果。基于商业定量实时 RT-PCR,RIDA® QUICK 诺如病毒检测法显示出高度显著的关联(p 值<0.001)和良好的一致性(kappa 值=0.6)。该检测法可检测到 3.22×10(6)至 3.26×10(8)拷贝/ml 范围内的粪便样本中的诺如病毒。在含有 5.9×10(6)拷贝/ml GI 型诺如病毒或 1.85×10(4)–4.28×10(5)拷贝/ml GII 型诺如病毒的粪便样本中出现假阴性结果。免疫层析 RIDA® QUICK 诺如病毒检测法可能有助于在发达国家和发展中国家快速筛查急性肠胃炎患者的诺如病毒感染,在这些国家,RT-PCR 方法尚未常规用于诊断。

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Evaluation of the RIDA(®)QUICK immunochromatographic norovirus detection assay using specimens from Australian gastroenteritis incidents.采用来自澳大利亚胃肠炎事件的标本评估 RIDA(®)QUICK 免疫层析诺如病毒检测试剂盒。
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