A Rapid Host Response Blood Test for Bacterial/Viral Infection Discrimination Using a Portable Molecular Diagnostic Platform.

IF 3.8 4区 医学 Q2 IMMUNOLOGY
Open Forum Infectious Diseases Pub Date : 2024-12-11 eCollection Date: 2025-01-01 DOI:10.1093/ofid/ofae729
Maria D Iglesias-Ussel, Nicholas O'Grady, Jack Anderson, Paul G Mitsis, Thomas W Burke, Ricardo Henao, Joseph Scavetta, Clare Camilleri, Sepideh Naderi, Amanda Carittini, Max Perelman, Rachel A Myers, Geoffrey S Ginsburg, Emily R Ko, Micah T McClain, Jesse van Westrienen, Ephraim L Tsalik, L Gayani Tillekeratne, Christopher W Woods
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引用次数: 0

Abstract

Background: Difficulty discriminating bacterial versus viral etiologies of infection drives unwarranted antibacterial prescriptions and, therefore, antibacterial resistance.

Methods: Utilizing a rapid portable test that measures peripheral blood host gene expression to discriminate bacterial and viral etiologies of infection (the HR-B/V assay on Biomeme's polymerase chain reaction-based Franklin platform), we tested 3 cohorts of subjects with suspected infection: the HR-B/V training cohort, the HR-B/V technical correlation cohort, and a coronavirus disease 2019 cohort.

Results: The Biomeme HR-B/V test showed very good performance at discriminating bacterial and viral infections, with a bacterial model accuracy of 84.5% (95% confidence interval [CI], 80.8%-87.5%), positive percent agreement (PPA) of 88.5% (95% CI, 81.3%-93.2%), negative percent agreement (NPA) of 83.1% (95% CI, 78.7%-86.7%), positive predictive value of 64.1% (95% CI, 56.3%-71.2%), and negative predictive value of 95.5% (95% CI, 92.4%-97.3%). The test showed excellent agreement with a previously developed BioFire HR-B/V test, with 100% (95% CI, 85.7%-100.0%) PPA and 94.9% (95% CI, 86.1%-98.3%) NPA for bacterial infection, and 100% (95% CI, 93.9%-100.0%) PPA and 100% (95% CI, 85.7%-100.0%) NPA for viral infection. Among subjects with acute severe acute respiratory syndrome coronavirus 2 infection of ≤7 days, accuracy was 93.3% (95% CI, 78.7%-98.2%) for 30 outpatients and 75.9% (95% CI, 57.9%-87.8%) for 29 inpatients.

Conclusions: The Biomeme HR-B/V test is a rapid, portable test with high performance at identifying patients unlikely to have bacterial infection, offering a promising antibiotic stewardship strategy that could be deployed as a portable, laboratory-based test.

利用便携式分子诊断平台进行细菌/病毒感染的快速宿主反应血液检测。
背景:难以区分细菌与病毒感染的病因导致无根据的抗菌药物处方,因此,抗菌药物耐药性。方法:利用检测外周血宿主基因表达的快速便携式检测方法(基于Biomeme聚合酶链反应的Franklin平台上的HR-B/V检测)区分感染的细菌和病毒病因,对疑似感染的3个队列进行检测:HR-B/V培训队列、HR-B/V技术相关队列和2019冠状病毒疾病队列。结果:Biomeme HR-B/V检测在区分细菌和病毒感染方面表现出非常好的性能,细菌模型准确率为84.5%(95%置信区间[CI], 80.8% ~ 87.5%),阳性一致性(PPA)为88.5% (95% CI, 81.3% ~ 93.2%),阴性一致性(NPA)为83.1% (95% CI, 78.7% ~ 86.7%),阳性预测值为64.1% (95% CI, 56.3% ~ 71.2%),阴性预测值为95.5% (95% CI, 92.4% ~ 97.3%)。该测试与先前开发的BioFire HR-B/V测试非常吻合,细菌感染的PPA为100% (95% CI, 85.7%-100.0%), NPA为94.9% (95% CI, 86.1%-98.3%),病毒感染的PPA为100% (95% CI, 93.9%-100.0%), NPA为100% (95% CI, 85.7%-100.0%)。在感染≤7天的急性严重急性呼吸综合征冠状病毒2型患者中,30例门诊患者的准确率为93.3% (95% CI, 78.7% ~ 98.2%), 29例住院患者的准确率为75.9% (95% CI, 57.9% ~ 87.8%)。结论:Biomeme HR-B/V检测是一种快速、便携的检测方法,在识别不太可能发生细菌感染的患者方面具有高性能,提供了一种有前途的抗生素管理策略,可以作为一种便携式、基于实验室的检测方法进行部署。
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来源期刊
Open Forum Infectious Diseases
Open Forum Infectious Diseases Medicine-Neurology (clinical)
CiteScore
6.70
自引率
4.80%
发文量
630
审稿时长
9 weeks
期刊介绍: Open Forum Infectious Diseases provides a global forum for the publication of clinical, translational, and basic research findings in a fully open access, online journal environment. The journal reflects the broad diversity of the field of infectious diseases, and focuses on the intersection of biomedical science and clinical practice, with a particular emphasis on knowledge that holds the potential to improve patient care in populations around the world. Fully peer-reviewed, OFID supports the international community of infectious diseases experts by providing a venue for articles that further the understanding of all aspects of infectious diseases.
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