比较诊断结核性脑膜炎的 DNA 提取方案和分子靶标。

Tuberculosis Research and Treatment Pub Date : 2017-01-01 Epub Date: 2017-05-30 DOI:10.1155/2017/5089046
Flavia Silva Palomo, Martha Gabriela Celle Rivero, Milene Gonçalves Quiles, Fernando Pereira Pinto, Antonia Maria de Oliveira Machado, Antonio Carlos Campos Pignatari
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引用次数: 0

摘要

结核性脑膜炎(TBM)是肺外结核病的一种严重形式。本研究旨在评估直接从 CSF 样本中提取 DNA 并通过 qPCR 扩增目标的内部分子诊断方案,以准确、快速地诊断 TBM。研究了 68 名疑似 TBM 患者的 100 份 CSF 样本。比较了四种 DNA 提取技术(酚-氯仿-硫氰酸胍法、硅硫氰酸胍法、树脂法和树脂加乙醇法),并利用 CSF 样本通过 qPCR 确定最佳靶点(IS6110、MPB64 和 hsp65 KDa)。在 PCR 扩增的定量和灵敏度方面,使用苯酚-氯仿-硫氰酸硅胍的提取方案显示出最佳结果,其 DNA 含量是第二最佳方案(硫氰酸硅胍)的 10 倍。对 TBM 诊断效果最好的靶标是 IS6110。当我们按样本分析结果时,该靶标显示出91%的灵敏度和97%的特异性;当我们按患者分析结果时,该靶标显示出100%的灵敏度和98%的特异性。在我们的临床实践中,使用酚-氯仿-硫氰酸胍进行DNA提取,然后进行IS6110靶标扩增已被证明适用于TBM的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of DNA Extraction Protocols and Molecular Targets to Diagnose Tuberculous Meningitis.

Tuberculous meningitis (TBM) is a severe form of extrapulmonary tuberculosis. The aims of this study were to evaluate in-house molecular diagnostic protocols of DNA extraction directly from CSF samples and the targets amplified by qPCR as an accurate and fast diagnosis of TBM. One hundred CSF samples from 68 patients suspected of TBM were studied. Four DNA extraction techniques (phenol-chloroform-thiocyanate guanidine, silica thiocyanate guanidine, resin, and resin with ethanol) were compared and CSF samples were used to determine the best target (IS6110, MPB64, and hsp65 KDa) by qPCR. The extraction protocol using the phenol-chloroform-thiocyanate guanidine showed the best results in terms of quantification and sensitivity of PCR amplification, presenting up to 10 times more DNA than the second best protocol, the silica guanidine thiocyanate. The target that showed the best result for TBM diagnosis was the IS6110. This target showed 91% sensitivity and 97% specificity when we analyzed the results by sample and showed 100% sensitivity and 98% specificity when we analyzed the results by patient. The DNA extraction with phenol-chloroform-thiocyanate guanidine followed by IS6110 target amplification has been shown to be suitable for diagnosis of TBM in our clinical setting.

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