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GeXPS 多重 PCR 分析培养细胞中增殖感染的猴痘病毒转录组和急性感染神经节。

GeXPS multiplex PCR analysis of the simian varicella virus transcriptome in productively infected cells in culture and acutely infected ganglia.

机构信息

Department of Neurology, University of Colorado Denver School of Medicine, 12700 East 19th Avenue, Mail Stop B182, Aurora, CO 80045, USA.

出版信息

J Virol Methods. 2013 Oct;193(1):151-8. doi: 10.1016/j.jviromet.2013.05.020. Epub 2013 Jun 11.

Abstract

Simian varicella zoster virus (SVV) infection of non-human primates serves as a model to study varicella zoster virus (VZV) infection and pathogenesis in humans. While macroarray analysis detected all 69 predicted unique open reading frames (ORFs) in SVV-infected cells in culture, it lacked the sensitivity to detect the low-abundance transcripts expressed in latently infected monkey ganglia. Recently, a multiplex RT-PCR assay using the GenomeLab Genetic Analysis System (GeXPS) identified 10 VZV transcripts in latently-infected human ganglia. GeXPS was used to analyze the SVV transcriptome in SVV-infected monkey cells in culture as well as in acutely infected ganglia from African green monkeys. Oligonucleotide primers containing both SVV ORF- and cell-specific sequences linked to universal DNA sequences were used in RT-PCR to produce products of predetermined sizes. Amplification products were resolved by capillary gel electrophoresis and detected by fluorescence spectrophotometry. Transcripts corresponding to all 69 predicted SVV ORFs, in addition to transcripts within the leftward end region and ORF 61 antisense transcripts were detected in virus-infected cells in culture. Except for two transcripts (ORFs 14 and 35), all transcripts found in infected tissue culture cells were also found in acutely infected monkey ganglia.

摘要

猿猴水痘带状疱疹病毒(SVV)感染非人类灵长类动物可作为研究人类水痘带状疱疹病毒(VZV)感染和发病机制的模型。虽然宏阵列分析检测到培养物中感染 SVV 的细胞中所有 69 个预测的独特开放阅读框(ORF),但其灵敏度不足以检测潜伏感染猴神经节中低丰度的转录本。最近,一种使用基因组实验室遗传分析系统(GeXPS)的多重 RT-PCR 检测法在潜伏感染的人神经节中鉴定出 10 种 VZV 转录本。GeXPS 用于分析培养物中感染 SVV 的猴细胞以及来自绿长尾猴的急性感染神经节中的 SVV 转录组。含有 SVV ORF 和细胞特异性序列并与通用 DNA 序列连接的寡核苷酸引物用于 RT-PCR 以产生预定大小的产物。扩增产物通过毛细管凝胶电泳分离,并通过荧光分光光度法检测。除了两个转录本(ORF14 和 35)之外,在培养物中感染的细胞中检测到所有预测的 69 个 SVV ORF 的转录本,以及在左向末端区域和 ORF61 反义转录本内的转录本。除了两个转录本(ORF14 和 35)之外,在感染组织培养细胞中发现的所有转录本也在急性感染的猴神经节中发现。

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