Division of Infectious Diseases, Department of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
J Clin Microbiol. 2012 Feb;50(2):364-71. doi: 10.1128/JCM.05996-11. Epub 2011 Nov 23.
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 (C(T)) 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.
FilmArray 呼吸道复合核酸检测试剂盒(RP)(Idaho Technology,盐湖城,犹他州)与实验室开发的实时 PCR 检测方法相比,可用于检测各种呼吸道病毒和某些细菌病原体。共检测了 215 份先前经实时 PCR 检测为一种或多种病原体阳性或阴性的冷冻存档儿科呼吸道标本。使用 FilmArray RP 系统检测结果与实时 PCR 检测方法的一致性为 98.6%(kappa = 0.92 [95%置信区间(CI),0.89 至 0.94])。共享分析物的联合阳性符合率为 89.4%(95%CI,85.4 至 92.6);阴性符合率为 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(C(T))值为 36.46 ± 4.54。当使用 FilmArray RP 时,其对合并感染的检测和对甲型流感病毒亚型的正确鉴定与实时 PCR 相当。在敏感性方面,比较差异最大的是腺病毒;24 份经实时 PCR 检测为腺病毒阳性的临床标本中,只有 11 份(45.8%;95%CI,27.9 至 64.9)也通过 FilmArray RP 检测为阳性。此外,在检测 20 种经高和低病毒载量制备的特征性腺病毒血清型时,FilmArray RP 既不能检测到 6 型和 41 型,也不能在病毒载量较低时检测到 2 型、20 型、35 型和 37 型。FilmArray RP 系统快速且易于使用,只需 1 个多小时即可得到结果,几乎不需要人工操作。然而,其低通量对于接收大量标本的实验室来说是一个显著的缺点,因为一次只能处理一个样本,且一次只能使用一台仪器。