A real-time PCR method to rapidly titer adenovirus stocks.

Maria A Thomas, Drew L Lichtenstein, Peter Krajcsi, William S M Wold
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引用次数: 24

Abstract

A critical step in working with adenovirus (Ad) and its vectors is the accurate, reproducible, sensitive, and rapid measurement of the amount of virus present in a stock. Titration methods fall into one of two categories: determination of either the infectious or the particle (infectious plus noninfectious) titer. Determining the infectious titer of a virus stock by plaque assay has important limitations, including cell line-, researcher-, and laboratory-dependent variation in titer, and the length of time required to perform the assay (2-4 wk). A major drawback of particle titration methods is the lack of consistent correlation between the resultant titer and the infectious titer. To overcome these problems, a rapid, sensitive, and reproducible real-time polymerase chain reaction (PCR) assay was developed that detects encapsidated full-length genomes. Importantly, there is a linear correlation between the titer determined by the realtime PCR assay and the infectious titer determined by a plaque assay. This chapter provides step-by-step guidance for preparing viral DNA, conducting the real-time PCR assay, and using the resultant data to calculate a viral titer.

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一种快速滴度腺病毒储备的实时PCR方法。
处理腺病毒(Ad)及其载体的关键步骤是准确、可重复、灵敏和快速地测量库存中存在的病毒数量。滴定法可分为两类:测定感染性滴度或颗粒(感染性加非感染性)滴度。通过空斑测定法测定病毒株的感染性滴度有重要的局限性,包括细胞系、研究人员和实验室的滴度差异,以及进行测定所需的时间(2-4周)。颗粒滴定法的一个主要缺点是所得滴度和感染滴度之间缺乏一致的相关性。为了克服这些问题,我们开发了一种快速、灵敏、可重复的实时聚合酶链反应(PCR)检测方法,用于检测封装的全长基因组。重要的是,实时PCR测定的滴度与空斑测定的感染滴度之间存在线性相关性。本章提供了一步一步的指导准备病毒DNA,进行实时PCR测定,并使用所得数据来计算病毒滴度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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