利用 HPV Direct Flow CHIP 系统检测福尔马林固定石蜡包埋标本中的人类乳头瘤病毒 DNA 并进行基因分型。

The Open Virology Journal Pub Date : 2013-10-18 eCollection Date: 2013-01-01 DOI:10.2174/1874357920130927004
Elsa Herraez-Hernandez, Ovidiu Preda, Sonia Alonso, Rosario Serrano Pardo, Asuncion Olmo
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引用次数: 0

摘要

用于人类乳头瘤病毒(HPV)基因分型的新型 HPV Direct Flow CHIP 商业系统基于快速 PCR 和基因型特异性探针的自动反向点印迹杂交,可检测 36 种 HPV 基因型。本研究检验了 HPV Direct Flow CHIP 在福尔马林固定石蜡包埋(FFPE)样本(n= 99)中的性能。对每个样本都进行了直接 PCR 分析(使用未经 DNA 纯化的粗细胞提取物)和传统 PCR 分析(使用纯化的 DNA)。对结果的配对分析表明,尽管传统 PCR 检测出的多重感染率略高,但这两种方法得出的结果非常一致。总之,HPV Direct Flow CHIP 能通过直接 PCR 和传统 PCR 方案从 FFPE 样品中有效检测 HPV。
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Detection and Genotyping of Human Papillomavirus DNA in Formalin-Fixed Paraffin-Embedded Specimens with the HPV Direct Flow CHIP System.

The novel HPV Direct Flow CHIP commercial system for Human Papillomavirus (HPV) genotyping is based on rapid PCR and automatic reverse dot blot hybridization to genotype-specific probes, allowing the detection of 36 HPV genotypes. This study examined the performance of HPV Direct Flow CHIP in formalin-fixed paraffin-embedded (FFPE) samples (n= 99). Each sample was analyzed both by Direct PCR, using crude cell extracts without DNA purification, and by conventional PCR, using purified DNA. Pair-wise analysis of the results demonstrated strong concordance between the results obtained with the two protocols, although a slightly higher rate of multiple infections was detected by conventional PCR. In summary, HPV Direct Flow CHIP achieves effective HPV detection from FFPE samples with both Direct PCR and Conventional PCR protocols.

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