单个细胞中腺病毒DNA和mRNA的原位检测

Tanel Punga, Sibel Ciftci, Mats Nilsson, Tomasz Krzywkowski
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引用次数: 2

摘要

DNA病毒如人腺病毒(HAdVs)的感染导致细胞群中病毒DNA和mRNA的高水平积累。然而,异质细胞群中病毒DNA和mRNA的平均含量并不一定反映单个细胞的丰度。由于绝大多数病毒感染研究是使用异质细胞群体的标准实验程序进行的,因此需要一种方法可以同时检测和定量分析群体内单个感染细胞中的病毒基因组积累和基因表达。本文描述了一种基于挂锁探针的滚动圈扩增方案,该方案允许同时检测hav 5型(hav -5) DNA和各种病毒编码的mRNA,以及在异质群体中的单个细胞中对hav -5 DNA拷贝和mRNA种类进行定量分析。这种多功能方法可用于检测不同细胞类型的致病性DNA病毒感染的程度,并延长感染时间。此外,在单个细胞中同时进行病毒DNA和mRNA的定量分析,可以鉴定出可能存在持续感染的细胞。©2018 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Situ Detection of Adenovirus DNA and mRNA in Individual Cells

Infection by DNA viruses such as human adenoviruses (HAdVs) causes a high-level accumulation of viral DNA and mRNA in the cell population. However, the average viral DNA and mRNA content in a heterogeneous cell population does not inevitably reflect the abundance in individual cells. As the vast majority of virus infection studies is carried out using standard experimental procedures with heterogeneous cell populations, there is a need for a method allowing simultaneous detection and quantitative analysis of viral genome accumulation and gene expression in individual infected cells within a population. This article describes a padlock probe–based rolling-circle amplification protocol that allows simultaneous detection of HAdV type 5 (HAdV-5) DNA and various virus-encoded mRNAs, as well as quantitative analysis of HAdV-5 DNA copies and mRNA species, in individual cells within a heterogeneous population. This versatile method can be used to detect the extent of pathogenic DNA virus infection in different cell types over prolonged infection times. Furthermore, simultaneous viral DNA and mRNA quantification in individual cells allows identification of cells in which persistent infections may be established. © 2018 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Microbiology
Current Protocols in Microbiology Immunology and Microbiology-Parasitology
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期刊介绍: Current Protocols in Microbiology provides detailed, step-by-step instructions for analyzing bacteria, animal and plant viruses, fungi, protozoans and other microbes. It offers updated coverage of emerging technologies and concepts, such as biofilms, quorum sensing and quantitative PCR, as well as proteomic and genomic methods. It is the first comprehensive source of high-quality microbiology protocols that reflects and incorporates the new mandates and capabilities of this robust and rapidly evolving discipline.
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