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Comparison of the Idaho Technology FilmArray System to Real-Time PCR for Detection of Respiratory Pathogens in Children

机译:爱达荷州技术FilmArray系统与实时PCR检测儿童呼吸道病原体的比较

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摘要

The FilmArray Respiratory Panel (RP) multiplexed nucleic acid amplification test (Idaho Technology, Inc., Salt Lake City, UT) was compared to laboratory-developed real-time PCR assays for the detection of various respiratory viruses and certain bacterial pathogens. A total of 215 frozen archived pediatric respiratory specimens previously characterized as either negative or positive for one or more pathogens by real-time PCR were examined using the FilmArray RP system. Overall agreement between the FilmArray RP and corresponding real-time PCR assays for shared analytes was 98.6% (kappa = 0.92 [95% confidence interval (CI), 0.89 to 0.94]). The combined positive percent agreement was 89.4% (95% CI, 85.4 to 92.6); the negative percent agreement was 99.6% (95% CI, 99.2 to 99.8). The mean real-time PCR threshold cycle (CT) value for specimens with discordant results was 36.46 ± 4.54. Detection of coinfections and correct identification of influenza A virus subtypes were comparable to those of real-time PCR when using the FilmArray RP. The greatest comparative difference in sensitivity was observed for adenovirus; only 11 of 24 (45.8%; 95% CI, 27.9 to 64.9) clinical specimens positive for adenovirus by real-time PCR were also positive by the FilmArray RP. In addition, upon testing 20 characterized adenovirus serotypes prepared at high and low viral loads, the FilmArray RP did not detect serotypes 6 and 41 at either level and failed to detect serotypes 2, 20, 35, and 37 when viral loads were low. The FilmArray RP system is rapid and extremely user-friendly, with results available in just over 1 h with almost no labor involved. Its low throughput is a significant drawback for laboratories receiving large numbers of specimens, as only a single sample can be processed at a time with one instrument.
机译:将FilmArray呼吸板(RP)多重核酸扩增测试(爱达荷州技术有限公司,爱荷华州盐湖城)与实验室开发的实时PCR分析进行了比较,以检测各种呼吸道病毒和某些细菌病原体。使用FilmArray RP系统检查了总共215份先前通过实时PCR鉴定为一种或多种病原体阴性或阳性的冰冻存档儿科呼吸道标本。对于共享的分析物,FilmArray RP和相应的实时PCR分析之间的总体一致性为98.6%(κ= 0.92 [95%置信区间(CI),0.89至0.94])。合并的正面同意率为89.4%(95%CI,85.4至92.6);负百分比一致性为99.6%(95%CI,99.2至99.8)。结果不一致的标本的平均实时PCR阈值循环(CT)值为36.46±4.54。使用FilmArray RP时,共感染的检测和正确鉴定A型流感病毒亚型与实时PCR相当。对于腺病毒,观察到敏感性的最大比较差异;通过实时PCR检出的腺病毒阳性临床样本中,只有24个样本中有11个样本(45.8%; 95%CI,27.9至64.9)也被FilmArray RP阳性。此外,在测试了在高和低病毒载量下制备的20种特征性腺病毒血清型时,FilmArray RP在两个水平上均未检测到血清型6和41,在病毒载量低时未能检测到血清型2、20、35和37。 FilmArray RP系统快速且极为用户友好,仅需1个小时以上即可获得结果,几乎无需人工。它的低通量对于实验室中接收大量标本的一个重大缺点,因为一次只能用一个仪器处理一个样品。

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