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BioCode 呼吸道病原体检测试剂盒对鼻咽拭子中病毒和细菌的临床检测性能。

The Clinical Performance of the BioCode Respiratory Pathogen Panel for the Detection of Viruses and Bacteria from Nasopharyngeal Swabs.

机构信息

Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Sichuan Academy of Medicine & Sichuan Provincial People's Hospital, Chengdu, China.

出版信息

Microbiol Spectr. 2023 Jun 15;11(3):e0404422. doi: 10.1128/spectrum.04044-22. Epub 2023 Apr 11.

Abstract

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.

摘要

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)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8051/10269715/e93b20373c03/spectrum.04044-22-f001.jpg

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