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

被引:1
|
作者
Zhang, Xin [1 ,2 ,3 ]
Knoth, Colleen [4 ,9 ]
Pham, Anh [4 ]
Lima, Amorce [5 ]
Dominguez, Rosario [6 ]
Ibarra-Flores, Irvin [6 ]
Lopez, Juan C. [1 ]
Uy, Dominic [5 ]
Silbert, Suzane [5 ]
Patel, Anami [8 ]
Aye, Michael [4 ]
Tang, Yi-Wei [1 ,10 ]
Dien Bard, Jennifer [6 ,7 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY USA
[2] Sichuan Acad Med, Chengdu, Peoples R China
[3] Sichuan Prov Peoples Hosp, Chengdu, Peoples R China
[4] Appl BioCode Inc, Santa Fe Springs, CA USA
[5] Tampa Gen Hosp, Tampa, FL USA
[6] Childrens Hosp Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90027 USA
[7] Univ Southern Calif, Keck Sch Med, Los Angeles, CA 90007 USA
[8] PathAI Diagnost, Memphis, TN USA
[9] Thermo Fisher Sci, San Diego, CA USA
[10] Danaher Diagnost Platform Cepheid China, Shanghai, Peoples R China
来源
MICROBIOLOGY SPECTRUM | 2023年 / 11卷 / 03期
关键词
respiratory pathogens; syndromic testing; multiplex PCR; scalable throughput; INFECTIONS; DISEASE; SINGLE; IMPACT;
D O I
10.1128/spectrum.04044-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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).IMPORTANCE 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.
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页数:11
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