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A sample-in-answer-out instrument for the detection of multiple respiratory pathogens in unprepared nasopharyngeal swab samples

机译:一种进样出仪器,用于检测未制备的鼻咽拭子样品中的多种呼吸道病原体

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Multiplex RT-PCR suspension array assays provide a powerful tool for identifying the causative agent(s) of respiratory infections. These assays are time consuming and laborious on a time-per-sample basis if only a few samples require processing. To address this shortcoming and provide an automated solution for fast detection and identification of viral pathogens, we developed the first automated multiplex RT-PCR suspension array instrument capable of handling unprepared clinical samples. The instrument requires less than 3 minutes of hands-on time for a result generated in 2.5 hours. In analytical studies, the instrument performed as well as manually performed assays. The performance of the instrument and loaded multiplex viral detection assay was then tested using unprepared nasopharyngeal samples. The instrument-performed assay detected 61 of 71 RSV positive samples, for a sensitivity of 85.9%. Adenovirus (n = 5) and influenza B (n = 3) were less prevalent in the sample set, but detected to similar levels, 80% and 75%, respectively. The same sample set was also tested using FDA approved immuno-assay rapid tests, and the instrument was found to be more sensitive than the rapid tests with the sole exception being influenza A (n = 16), which was poorly detected due to significant sequence mismatches between the influenza A primer/probe set included in the multiplex mixture and the circulating influenza A strains. Overall, these data demonstrate the developed prototype platform performs multiplex array assays as well as hand-performed assays, and that the instrument's sensitivity and specificity are dictated by the quality of the loaded multiplex assay.
机译:多重RT-PCR悬浮液阵列测定法为鉴定呼吸道感染的病因提供了强大的工具。如果仅需要处理几个样品,则这些测定是耗时且费时的。为了解决此缺点,并提供一种用于快速检测和鉴定病毒病原体的自动化解决方案,我们开发了第一台能够处理未制备的临床样品的自动化多重RT-PCR悬浮液阵列仪器。仪器需要不到3分钟的动手时间才能在2.5小时内产生结果。在分析研究中,仪器的性能与手动分析相同。然后使用未制备的鼻咽样品测试仪器和装载的多重病毒检测测定的性能。仪器执行的测定法检测了71个RSV阳性样品中的61个,灵敏度为85.9%。腺病毒(n = 5)和乙型流感(n = 3)在样本集中不那么普遍,但检出水平相近,分别为80%和75%。还使用FDA批准的免疫测定快速测试方法测试了同一样本集,发现该仪器比快速测试方法更敏感,唯一的例外是甲型流感(n = 16),由于序列很长而无法检测到多重混合物中包含的A型流感引物/探针组与正在传播的A型流感病毒株之间的错配。总体而言,这些数据表明,开发的原型平台可以执行多重阵列测定以及手动执行的测定,并且仪器的灵敏度和特异性取决于所装载的多重测定的质量。

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