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首页> 外文期刊>Journal of Medical Virology >Detection of Influenza by Real Time RT-PCR Is Not Affected by Delays in Respiratory Specimen Processing
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Detection of Influenza by Real Time RT-PCR Is Not Affected by Delays in Respiratory Specimen Processing

机译:通过实时RT-PCR检测流感不受呼吸道标本处理过程中的延迟影响

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摘要

Sample processing for real-time reverse transcriptase polymerase chain reaction (rRT-PCR) based diagnostic assays requires stabilizing sample ribonucleic acid (RNA) in lysis buffer prior to testing. The stability of viral RNA prior to processing is difficult to assure. It is unknown whether clinical sample integrity is compromised by delays in processing, as may occur due to weekends and holidays. We sought to examine the integrity of respiratory specimens with variable processing times. Upper respiratory specimens were collected during three influenza seasons 20092012 and tested for influenza virus and internal control human RNase P (RNP) RNA by rRT-PCR. Time to processing was measured in hours from specimen collection to placement in lysis buffer. Six hundred thirty-five (11.4%) of 5,583 samples were influenza positive. Mean and median times to processing were 11.5 hr and 6.0 hr, respectively (min 0.1 hr, max 105.2 hr). There were no significant associations between time to processing and presence of RNP (OR = 1.0, P = 0.740), or detection of influenza (OR = 1.0, P = 0.060). Longer duration of illness was associated with a lower likelihood of influenza detection (OR = 0.92, P < 0.001) and with increased influenza A cycle threshold (Ct) values (P< 0.001), while older age was associated with increased influenza B Ct values (P = 0.001), indicating the presence of less amplifiable RNA. Delays in time to processing of upper respiratory specimens up to 105 hr were not associated with decreased detection of amplifiable RNA, suggesting specimen integrity is not compromised by such delays. (C) 2016 Wiley Periodicals, Inc.
机译:基于实时逆转录酶聚合酶链反应(rRT-PCR)的诊断分析的样品处理需要在测试前稳定裂解缓冲液中的样品核糖核酸(RNA)。难以确定加工前病毒RNA的稳定性。尚不知道临床样品的完整性是否会因周末和节假日的处理延迟而受到损害。我们试图通过变化的处理时间来检查呼吸道标本的完整性。在三个流感季节20092012期间收集上呼吸道标本,并通过rRT-PCR检测流感病毒和内部对照人类RNase P(RNP)RNA。从样品收集到裂解缓冲液放置的小时数,计算处理时间。 5,583个样本中有635个(11.4%)为流感阳性。处理的平均时间和中位数时间分别为11.5小时和6.0小时(最小0.1小时,最大105.2小时)。加工时间与RNP的存在(OR = 1.0,P = 0.740)或检测到流感(OR = 1.0,P = 0.060)之间没有显着关联。疾病持续时间越长,流感检测的可能性越低(OR = 0.92,P <0.001),流感A循环阈值(Ct)值升高(P <0.001),而年龄越大,流感B Ct值升高则相关。 (P = 0.001),表明存在扩增较少的RNA。上呼吸道标本处理时间最多延迟105小时与可扩增RNA的检测减少无关,这表明标本完整性不受此类延迟影响。 (C)2016威利期刊公司

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