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Partial comparison of the NxTAG Respiratory Pathogen Panel Assay with the Luminex xTAG Respiratory Panel Fast Assay V2 and singleplex real-time polymerase chain reaction for detection of respiratory pathogens

机译:NxTAG呼吸道病原体测定与Luminex xTAG呼吸道快速测定V2和单重实时聚合酶链反应检测呼吸道病原体的部分比较

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In this study, 185 nasopharyngeal swabs were tested to compare the sensitivity and specificity of the Luminex NxTAG (NxTAG) Respiratory Pathogen Panel (RPP) Assay with those of the Luminex Respiratory Virus Panel (RVP) Fast Assay v2 and singleplex real-time polymerase chain reaction (PCR). The NxTAG Assay identified at least one infectious agent in 164 (88.7%) of the swabs. In 91 (6.2%) tests with negative results with the RVP Fast Assay v2, a virus was identified by the NxTAG (P < 0.001). With the NxTAG Assay, the detection rates were significantly higher for respiratory syncytial virus (P = 0.003), human metapneumovirus (P < 0.001), human rhinovirus/human enterovirus (P = 0.009) and human adenovirus (P < 0.001). Finally, the NxTAG Assay identified M. pneumoniae in 32 of 44 (72.7%) PCR-positive samples. However, the concordance with real-time PCR results was low for both assays. In conclusion, the results indicate that the NxTAG Assay overcomes some of the limitations of previous Luminex assays, although further studies are needed for a more complete evaluation of the new assay. (C) 2016 Elsevier Inc. All rights reserved.
机译:在这项研究中,对185支鼻咽拭子进行了测试,以比较Luminex NxTAG(NxTAG)呼吸道病原体组(RPP)测定法与Luminex呼吸道病毒组(RVP)快速测定法v2和单重实时聚合酶链反应的敏感性和特异性。反应(PCR)。 NxTAG分析在164个(88.7%)拭子中鉴定出至少一种传染原。在91个(6.2%)RVP快速检测v2的测试结果为阴性的情况下,通过NxTAG鉴定出病毒(P <0.001)。使用NxTAG分析时,呼吸道合胞病毒(P = 0.003),人间质肺病毒(P <0.001),人鼻病毒/人肠病毒(P = 0.009)和人腺病毒(P <0.001)的检出率明显更高。最后,NxTAG分析在44个(72.7%)PCR阳性样品中的32个中鉴定出肺炎支原体。但是,两种检测方法与实时PCR结果的一致性均很低。总之,结果表明NxTAG分析克服了先前Luminex分析的某些局限性,尽管需要进一步研究以更全面地评估新分析。 (C)2016 Elsevier Inc.保留所有权利。

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