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一种使用IncuCyte ZOOM测量丙型肝炎病毒感染滴度的新方法及其在抗病毒筛选中的应用。

A novel method for the measurement of hepatitis C virus infectious titres using the IncuCyte ZOOM and its application to antiviral screening.

作者信息

Stewart Hazel, Bartlett Christopher, Ross-Thriepland Douglas, Shaw Joseph, Griffin Stephen, Harris Mark

机构信息

School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.

Leeds Institute of Cancer and Pathology, Faculty of Medicine and Health, St James's University Hospital, University of Leeds, Leeds LS9 7TF, United Kingdom.

出版信息

J Virol Methods. 2015 Jun 15;218:59-65. doi: 10.1016/j.jviromet.2015.03.009. Epub 2015 Mar 20.

Abstract

Hepatitis C virus (HCV) is a significant human pathogen infecting 3% of the world population. An infectious molecular clone capable of replicating and releasing infectious virions in cell culture has only been available since 2005, leaving a significant knowledge gap concerning post-RNA replication events such as particle assembly, trafficking and release. Thus, a fast, efficient and accurate method of measuring infectious viral titres is highly desirable. Current methods rely upon manual counting of infected cell foci and so are both labour-intensive and susceptible to human error. Here, we report a novel protocol, which utilises the IncuCyte ZOOM instrument and related software to accurately count infected cells and extrapolation of this data to produce an infectious titre, reported as infectious units per millilitre (IU/mL). This method reduces cost, time and error in experiments. We also demonstrate that this approach is amenable to high-throughput compound screening, thereby expediting the identification of novel antivirals.

摘要

丙型肝炎病毒(HCV)是一种重要的人类病原体,全球3%的人口受其感染。直到2005年才出现一种能够在细胞培养中复制并释放传染性病毒粒子的感染性分子克隆,这使得在RNA复制后事件(如病毒颗粒组装、运输和释放)方面存在重大知识空白。因此,非常需要一种快速、高效且准确的测量传染性病毒滴度的方法。目前的方法依赖于人工计数受感染的细胞病灶,因此既耗费人力,又容易出现人为误差。在此,我们报告一种新方案,该方案利用IncuCyte ZOOM仪器和相关软件准确计数受感染细胞,并根据这些数据推断得出传染性滴度,以每毫升传染性单位(IU/mL)表示。这种方法降低了实验成本、时间和误差。我们还证明,这种方法适用于高通量化合物筛选,从而加快新型抗病毒药物的鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/135f/4411217/4ce1e57883a2/gr1.jpg

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