Development of a rapid point-of-care dengue virus type 2 infection diagnostic assay using recombinase polymerase amplification and lateral flow device.

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-05-14 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1578549
Meagan A Prescott, Myra T Koesdjojo, David T Mandrell, Manoj K Pastey
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引用次数: 0

Abstract

Introduction: Dengue virus (DENV) is the most rapidly spreading arbovirus globally, with over half of the world's population at risk of infection. Early and rapid detection is crucial to ensure timely patient care, reduce healthcare burden, and prevent severe disease progression. However, conventional nucleic acid amplification techniques are often unsuitable for low-resource settings due to their equipment and procedural demands.

Methods: We evaluated a real-time reverse transcription recombinase polymerase amplification (RT-RPA) assay for the sensitive and specific detection of DENV serotype 2 (DENV2). The assay was tested using both Twista fluorometer and lateral flow detection (LFD) formats. Analytical sensitivity was determined by probit regression, while specificity was assessed against unrelated viruses and other flaviviruses. Clinical validation was performed using serum, cell culture, and FTA® card samples. Assay robustness was evaluated under varying temperatures and after freeze-thaw cycles.

Results: The RT-RPA assay reliably amplified DENV2 at concentrations as low as 50 copies per reaction, with LOD₉₅ estimated at 38.48 copies (Twista) and 50.37 copies (LFD). No cross-reactivity was observed with respiratory syncytial virus, influenza, rabbit herpes virus, West Nile virus, or other DENV serotypes (DENV1, DENV3, DENV4). The assay successfully detected multiple DENV2 strains and maintained performance across 33°C-40°C and after repeated freeze-thaw cycles. RNA extracted from FTA® cards was successfully amplified. Clinical validation confirmed accurate detection in serum and cell culture samples, while DENV3-positive blood samples tested negative, reinforcing specificity.

Discussion: The RT-RPA/LFD assay offers a rapid, sensitive, and specific tool for DENV2 detection, compatible with low-resource and field-based settings. Its simplicity, robustness, and portability make it a promising approach for point-of-care diagnostics and outbreak surveillance in endemic regions.

利用重组酶聚合酶扩增和侧流装置建立快速护理点登革病毒2型感染诊断试验。
登革热病毒(DENV)是全球传播最迅速的虫媒病毒,世界上一半以上的人口面临感染风险。早期和快速检测对于确保及时护理患者、减轻医疗负担和预防严重疾病进展至关重要。然而,传统的核酸扩增技术由于其设备和程序要求,往往不适合资源匮乏的环境。方法:我们评估了实时逆转录重组酶聚合酶扩增(RT-RPA)检测DENV血清2型(DENV2)的敏感性和特异性。使用Twista荧光计和横向流量检测(LFD)格式对该分析进行了测试。通过概率回归确定分析敏感性,同时评估对无关病毒和其他黄病毒的特异性。使用血清、细胞培养和FTA®卡片样本进行临床验证。在不同温度和冻融循环后,评估了测定的稳健性。结果:RT-RPA测定可靠地扩增DENV2,每次反应的浓度低至50个拷贝,LOD₉₅估计为38.48个拷贝(Twista)和50.37个拷贝(LFD)。未观察到与呼吸道合胞病毒、流感病毒、兔疱疹病毒、西尼罗河病毒或其他DENV血清型(DENV1、DENV3、DENV4)的交叉反应性。该试验成功检测到多种DENV2菌株,并在33°C-40°C和反复冻融循环后保持性能。从FTA®卡中提取的RNA被成功扩增。临床验证证实了血清和细胞培养样本的准确检测,而denv3阳性血液样本检测为阴性,增强了特异性。讨论:RT-RPA/LFD检测提供了一种快速、敏感和特异性的DENV2检测工具,与低资源和现场环境兼容。它的简单性、稳健性和可移植性使其成为流行地区即时诊断和疫情监测的一种有前景的方法。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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