Rapid, inexpensive multiplex pathogen detection using resequencing microarrays.

IF 2.2 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS Journal of virological methods Pub Date : 2025-01-16 DOI:10.1016/j.jviromet.2025.115109
Kendall Hoff, Xun Ding, Xing Liang Liu, Ju-Yu Lin, John Duque, Su Yu, Samantha Dung, Filip Crnogorac, Glenn McGall, Jie Duan, John Chiang, Jeremy Edwards, Wei Zhou
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Abstract

Humanity faces an ongoing battle at the microscopic level to identify, contain, and treat outbreaks of numerous pathogens each year. Global genomic surveillance is the first step in monitoring outbreaks, but high-throughput methods are expensive and time-consuming. To solve this problem, we designed and manufactured a resequencing microarray capable of identifying 35 viral pathogens, 21 pathogenic bacteria, 16 antibiotic resistance genes, and 6 controls. We then developed an assay using these microarrays for the rapid detection of SARS-CoV-2, influenza A, and influenza B. Here, we present the clinical validation data for this test. The assay requires less than two hours to complete and has high-sensitivity, with limits of detection of 125 copies per mL for SARS-CoV-2, 0.01-0.05 TCID50/mL for influenza A, and 0.005-0.01 TCID50/mL for influenza B. The microarrays used for these assays are easily mass-produced using wafer-scale synthesis, making this an affordable option for pathogen screening with broad implications in public health.

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快速,廉价的多重病原体检测使用重测序微阵列。
人类每年在微观层面上面临着一场持续的战斗,以识别、控制和治疗大量病原体的爆发。全球基因组监测是监测疫情的第一步,但高通量方法既昂贵又耗时。为了解决这个问题,我们设计并制造了一种重测序芯片,能够识别35种病毒病原体,21种致病菌,16种抗生素耐药基因和6种对照。然后,我们利用这些微阵列开发了一种检测方法,用于快速检测SARS-CoV-2、甲型流感和乙型流感。在这里,我们提出了该测试的临床验证数据。该检测只需不到两个小时即可完成,灵敏度高,SARS-CoV-2的检测限为125拷贝/mL,甲型流感的检测限为0.01-0.05 TCID50/mL,乙型流感的检测限为0.005-0.01 TCID50/mL。用于这些检测的微阵列很容易通过晶圆规模合成进行批量生产,使其成为一种经济实惠的病原体筛查选择,在公共卫生方面具有广泛的意义。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
期刊最新文献
Performance evaluation of TaqMan™ Arbovirus Triplex Kit (ZIKV/DENV/CHIKV) for detection and differentiation of dengue and chikungunya viral RNA in serum samples of symptomatic patients. Climatic determinants of monkeypox transmission: A multi-national analysis using generalized count mixed models. Rapid, inexpensive multiplex pathogen detection using resequencing microarrays. Enhancing lumpy skin disease control: Effective competitive and indirect ELISAs for serological surveillance. Construction and verification of an infectious cDNA clone of encephalomyocarditis virus from pigs.
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