Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905.
Diagn Microbiol Infect Dis. 2020 Jun;97(2):115014. doi: 10.1016/j.diagmicrobio.2020.115014. Epub 2020 Feb 7.
Viral respiratory infections remain a significant cause of morbidity and mortality in pediatric, elderly, and immunocompromised patients. The Panther Fusion respiratory panels consist of 3 separate multiplex assays that test for 1) influenza A, influenza B, and RSV; 2) parainfluenza virus types 1-4; or 3) adenovirus, human metapneumovirus, and rhinovirus. This study evaluated the performance of the Fusion assays for both upper and lower respiratory tract specimens in comparison to routine methods, including viral culture and targeted real-time polymerase chain reaction assays. Following discordant resolution, the Fusion assays demonstrated high overall correlation (98.6% [648/657]) with routine methods. In addition, prospective testing of respiratory specimens (n = 146) submitted for viral culture showed a ~10-fold increase in detection by the Fusion panels compared to viral culture (28.1% versus 2.7% positivity). The Fusion respiratory panels offer a flexible, more targeted approach to respiratory virus testing with a turnaround time comparable to other molecular assays.
病毒呼吸道感染仍然是儿科、老年和免疫功能低下患者发病率和死亡率的重要原因。 Panther Fusion 呼吸道检测试剂盒包含 3 种单独的多重检测方法,用于检测 1)甲型流感、乙型流感和 RSV;2)副流感病毒 1-4 型;或 3)腺病毒、人偏肺病毒和鼻病毒。本研究评估了 Fusion 检测试剂盒在上呼吸道和下呼吸道标本与常规方法(包括病毒培养和靶向实时聚合酶链反应检测)相比的性能。经过不一致性解决后,Fusion 检测试剂盒与常规方法具有高度的总体相关性(98.6%[657/648])。此外,对提交进行病毒培养的呼吸道标本(n=146)进行前瞻性检测显示,与病毒培养相比,Fusion 检测试剂盒的检测阳性率增加了约 10 倍(28.1%比 2.7%)。Fusion 呼吸道检测试剂盒提供了一种灵活、更具针对性的呼吸道病毒检测方法,其检测周转时间与其他分子检测方法相当。