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Assessment of the inhibition of Dengue virus infection by carrageenan via real-time monitoring of cellular oxygen consumption rates within a microfluidic device

机译:通过实时监测微流控设备中细胞耗氧率评估卡拉胶对登革热病毒的抑制作用

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摘要

A microfluidic device combined with a light modulation system was developed to assess the inhibitory effect of carrageenan on Dengue virus (DENV) infection via real-time monitoring of cellular oxygen consumption rates (OCRs). Measuring cellular OCRs, which can reflect cellular metabolic activity, enabled us to monitor the process of viral infection in real time and to rapidly determine the antiviral activity of potential drugs/chemical compounds. The time variation of the cellular OCR of single cells that were infected in situ by DENV at different multiplicity of infection (m.o.i.) values was first successfully measured within a microfluidic device. The influence of the timing of carrageenan treatment on DENV infection was then examined by real-time monitoring of cellular OCRs in three groups. Cells that were pre-treated with carrageenan and then infected with DENV served as a pre-treatment group, cells to which carrageenan was added simultaneously with DENV served as a virucide group, and cells that were pre-infected with DENV and then treated with carrageenan served as a post-treatment group. By monitoring cellular OCRs, we could rapidly evaluate the inhibitory effect of carrageenan on DENV infection, obtaining a result within 7 h and showing that carrageenan had strong and effective anti-DENV activity in the three groups. In particular, a strong inhibitory effect was observed in the virucide group. Moreover, once the virus enters host cells in the post-treatment group, the immediate treatment with carrageenan for the infected cells has higher efficiency of antiviral activity. Our proposed platform enables to perform time-course or dose-response measurements of changes in cellular metabolic activity caused by diseases, chemical compounds, and drugs via monitoring of the cellular OCR, with rapid and real-time detection. This approach provides the potential to study a wide range of biological applications in cell-based biosensing, toxicology, and drug discovery.
机译:开发了一种与光调制系统结合的微流控设备,以通过实时监测细胞耗氧率(OCR)来评估角叉菜胶对登革热病毒(DENV)的抑制作用。通过测量可反映细胞代谢活性的细胞OCR,我们可以实时监控病毒感染的过程并快速确定潜在药物/化合物的抗病毒活性。首先在微流控设备中成功地测量了在不同的感染复数(m.o.i.)值下被DENV原位感染的单个细胞的细胞OCR的时间变化。然后通过实时监测三组细胞中的OCR来检查角叉菜胶治疗时间对DENV感染的影响。先用角叉菜胶预处理,然后用DENV感染的细胞作为预处理组,将同时添加角叉菜胶和DENV的细胞作为抗病毒剂组,将用DENV预先感染然后再用角叉菜胶处理的细胞担任后治疗组。通过监测细胞OCRs,我们可以快速评估角叉菜胶对DENV感染的抑制作用,在7h内获得结果,表明角叉菜胶在三组中均具有强大而有效的抗DENV活性。特别地,在杀病毒剂组中观察到强抑制作用。此外,一旦病毒进入后处理组的宿主细胞,立即用角叉菜胶对被感染的细胞进行处理具有更高的抗病毒活性。我们提出的平台能够通过监视细胞OCR进行快速,实时检测,从而对由疾病,化合物和药物引起的细胞代谢活性变化进行时程或剂量响应测量。这种方法为研究基于细胞的生物传感,毒理学和药物发现中的广泛生物学应用提供了潜力。

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