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通过实时逆转录聚合酶链反应从尿液样本中检测登革病毒。

Recovery of dengue virus from urine samples by real-time RT-PCR.

作者信息

Van den Bossche D, Cnops L, Van Esbroeck M

机构信息

Central Laboratory of Clinical Biology, Department of Clinical Sciences, Institute of Tropical Medicine (ITM), Kronenburgstraat 43/3, 2000, Antwerp, Belgium,

出版信息

Eur J Clin Microbiol Infect Dis. 2015 Jul;34(7):1361-7. doi: 10.1007/s10096-015-2359-0. Epub 2015 Mar 21.

Abstract

Recently, reverse transcription polymerase chain reaction (RT-PCR) for dengue virus (DENV) has been reported to test positive in urine samples for a longer time frame than in serum. We evaluated two RNA extraction procedures from urine and investigated the stability of DENV RNA in urine and serum up to 1 year at different storage temperatures. In addition, 24 urine samples collected from patients with a recent infection were tested with DENV real-time RT-PCR and compared to the RT-PCR results on serum. Five patients with an acute DENV infection were followed up for 6 months by RT-PCR on urine. The automated extraction method with the MagNA Pure LC 2.0 device had a higher yield of DENV RNA compared to the manual QIAGEN method, explained by the higher volume used in the former method. DENV RNA in both serum and urine was stable at room temperature up to 1 month and at 4 °C and -20 °C for at least 1 year. The detection rate by RT-PCR on urine was 50 % (4/8) until day 7, 100 % (6/6) between 1 and 3 weeks after symptom onset, and 25 % (2/8) thereafter. Generally, DENV RNA concentrations are higher in serum than in urine up till day 7, switching to lower concentrations in serum thereafter. Peak concentrations in urine are reached around day 10, and RNA becomes undetectable 3 to 4 weeks following disease onset. This diagnostic tool is of added value in clinical settings by extending the period during which DENV infections are diagnosed by RT-PCR.

摘要

最近有报道称,登革病毒(DENV)的逆转录聚合酶链反应(RT-PCR)在尿液样本中呈阳性的时间比血清样本更长。我们评估了两种从尿液中提取RNA的方法,并研究了在不同储存温度下DENV RNA在尿液和血清中长达1年的稳定性。此外,对近期感染患者采集的24份尿液样本进行了DENV实时RT-PCR检测,并与血清样本的RT-PCR结果进行比较。对5例急性DENV感染患者通过尿液RT-PCR进行了6个月的随访。与手动QIAGEN方法相比,使用MagNA Pure LC 2.0设备的自动提取方法DENV RNA产量更高,这是因为前者使用的样本量更大。血清和尿液中的DENV RNA在室温下可稳定保存1个月,在4℃和-20℃下至少可稳定保存1年。症状出现后第7天,尿液RT-PCR检测率为50%(4/8),1至3周时为100%(6/6),之后为25%(2/8)。一般来说,直到第7天血清中的DENV RNA浓度高于尿液,之后血清中的浓度则较低。尿液中的峰值浓度在第10天左右达到,发病后3至4周RNA检测不到。通过延长RT-PCR诊断DENV感染的时间,这种诊断工具在临床环境中具有附加价值。

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