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采用广谱聚合酶链反应检测腹膜炎患者持续非卧床腹膜透析液中病原菌的 DNA 提取方法评估及其临床应用。

Evaluation of DNA extraction methods and their clinical application for direct detection of causative bacteria in continuous ambulatory peritoneal dialysis culture fluids from patients with peritonitis by using broad-range PCR.

机构信息

Department of Laboratory Medicine, Inje University College of Medicine, Busan, Korea.

出版信息

Ann Lab Med. 2012 Mar;32(2):119-25. doi: 10.3343/alm.2012.32.2.119. Epub 2012 Feb 23.

Abstract

BACKGROUND

The aims of this study were to compare several DNA extraction methods and 16S rDNA primers and to evaluate the clinical utility of broad-range PCR in continuous ambulatory peritoneal dialysis (CAPD) culture fluids.

METHODS

Six type strains were used as model organisms in dilutions from 10(8) to 10(0) colony-forming units (CFU)/mL for the evaluation of 5 DNA extraction methods and 5 PCR primer pairs. Broad-range PCR was applied to 100 CAPD culture fluids, and the results were compared with conventional culture results.

RESULTS

There were some differences between the various DNA extraction methods and primer sets with regard to the detection limits. The InstaGene Matrix (Bio-Rad Laboratories, USA) and Exgene Clinic SV kits (GeneAll Biotechnology Co. Ltd, Korea) seem to have higher sensitivities than the others. The results of broad-range PCR were concordant with the results from culture in 97% of all cases (97/100). Two culture-positive cases that were broad-range PCR-negative were identified as Candida albicans, and 1 PCR-positive but culture-negative sample was identified as Bacillus circulans by sequencing. Two samples among 54 broad-range PCR-positive products could not be sequenced.

CONCLUSIONS

There were differences in the analytical sensitivity of various DNA extraction methods and primers for broad-range PCR. The broad-range PCR assay can be used to detect bacterial pathogens in CAPD culture fluid as a supplement to culture methods.

摘要

背景

本研究旨在比较几种 DNA 提取方法和 16S rDNA 引物,并评估广谱 PCR 在持续非卧床腹膜透析(CAPD)培养物中的临床应用价值。

方法

以 6 株标准菌株为模型生物,稀释度为 10(8)至 10(0)菌落形成单位(CFU)/mL,用于评估 5 种 DNA 提取方法和 5 对 PCR 引物。将广谱 PCR 应用于 100 份 CAPD 培养物,并将结果与传统培养结果进行比较。

结果

不同的 DNA 提取方法和引物在检测限方面存在一些差异。InstaGene Matrix(美国 Bio-Rad 实验室)和 Exgene Clinic SV 试剂盒(韩国 GeneAll 生物技术有限公司)似乎比其他试剂盒具有更高的灵敏度。广谱 PCR 的结果与培养结果在 97%的病例中一致(97/100)。两种培养阳性而广谱 PCR 阴性的病例被鉴定为白色念珠菌,1 种 PCR 阳性但培养阴性的样本通过测序鉴定为环状芽孢杆菌。在 54 个广谱 PCR 阳性产物中,有 2 个无法进行测序。

结论

不同的 DNA 提取方法和广谱 PCR 引物在分析灵敏度方面存在差异。广谱 PCR 检测方法可作为培养方法的补充,用于检测 CAPD 培养物中的细菌病原体。

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