Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sichuan Academy of Medicine & Sichuan Provincial People's Hospital, Chengdu, China.
Microbiol Spectr. 2023 Jun 15;11(3):e0404422. doi: 10.1128/spectrum.04044-22. Epub 2023 Apr 11.
Early detection of microbial pathogens causing respiratory tract infection plays a crucial role in clinical management. The BioCode Respiratory Pathogen Panel (BioCode RPP) utilizes reverse transcriptase PCR (RT-PCR) in combination with barcoded magnetic beads to amplify, detect, and identify respiratory pathogens. This panel qualitatively detects and identifies 14 viruses, including influenza virus A with H1 pdm09, H1, and H3 subtyping; influenza B; respiratory syncytial virus (RSV); human metapneumovirus; parainfluenza virus 1; parainfluenza virus 2; parainfluenza virus 3; parainfluenza virus 4; coronavirus (229E, NL63, OC43, and HKU1); adenovirus; and human rhinovirus/enterovirus, and 3 bacteria, including Chlamydia pneumoniae, Mycoplasma pneumoniae, and Bordetella pertussis. Reproducibility, which was assessed with contrived specimens containing 12 targets at 3 clinical sites, with 2 operators at each site for 5 days, was 99.4% for Flu A H3 and Flu B, 98.9% for RSV, and 100% for the remaining 9 targets assayed. A multicenter clinical trial evaluated the performance of the BioCode RPP with 2,647 nasopharyngeal swab specimens from 5 geographically distinct sites and revealed comparable performance between the BioCode RPP and FilmArray Respiratory Panel (FA-RP). Specifically, the positive percent agreements (PPAs) for various pathogens ranged between 80.8% and 100% compared with the FA-RP (1.7 and 2.0). Negative percent agreement ranged from 98.4% to 100% for BioCode RPP. The BioCode RPP also offers scalable automated testing capability of up to 96 specimens in a single run with total sample-to-result time under 5 h. The invalid rate of the BioCode RPP on initial testing was 1.0% (26/2,649). Early detection of microbial pathogens causing respiratory tract infection plays a crucial role in clinical management. The BioCode Respiratory Pathogen Panel (BioCode RPP) is a high-throughput test that utilizes RT-PCR in combination with barcoded magnetic beads to amplify, detect, and identify 17 respiratory pathogens, including 14 viruses and 3 bacteria. This study summarizes data generated from a multicenter clinical trial evaluating the performance of the BioCode RPP on 2,647 nasopharyngeal swab specimens from five geographically distinct sites.
呼吸道感染病原体的早期检测在临床管理中起着至关重要的作用。BioCode 呼吸道病原体检测试剂盒(BioCode RPP)采用逆转录聚合酶链反应(RT-PCR)与带条码的磁珠相结合的方法来扩增、检测和鉴定呼吸道病原体。该试剂盒定性检测和鉴定了 14 种病毒,包括流感病毒 A(具有 H1 pdm09、H1 和 H3 亚型)、流感 B、呼吸道合胞病毒(RSV)、人偏肺病毒、副流感病毒 1、副流感病毒 2、副流感病毒 3、副流感病毒 4、冠状病毒(229E、NL63、OC43 和 HKU1)、腺病毒和人鼻病毒/肠道病毒,以及 3 种细菌,包括肺炎衣原体、肺炎支原体和百日咳博德特菌。在三个临床地点,由 12 个目标组成的人工样本,由每个地点的两名操作人员在 5 天内进行评估,结果显示 Flu A H3 和 Flu B 的重复性为 99.4%,RSV 为 98.9%,其余 9 个检测目标的重复性为 100%。一项多中心临床试验评估了 BioCode RPP 在 5 个地理位置不同的地点采集的 2647 份鼻咽拭子标本的性能,结果显示 BioCode RPP 与 FilmArray 呼吸道病原体检测试剂盒(FA-RP)的性能相当。具体来说,与 FA-RP 相比,各种病原体的阳性百分比一致率(PPA)在 80.8%至 100%之间(1.7 和 2.0)。BioCode RPP 的阴性百分比一致率为 98.4%至 100%。BioCode RPP 还具有可扩展的自动化测试能力,在单个运行中最多可处理 96 个样本,总样本到结果的时间不到 5 小时。BioCode RPP 初始检测的无效率为 1.0%(26/2649)。