Comparison of manual and automated nucleic acid extraction methods from clinical specimens for microbial diagnosis purposes

被引:5
作者
Wozniak, Aniela [1 ]
Geoffroy, Enrique [1 ]
Miranda, Carolina [1 ]
Castillo, Claudia [1 ]
Sanhueza, Francia [1 ]
Garcia, Patricia [1 ]
机构
[1] Pontificia Univ Catolica Chile, Escuela Med, Dept Labs Clin, Microbiol Lab, Santiago, Chile
关键词
MagNA Pure; Molecular diagnosis; Nucleic acid extraction methods; Microbial pathogens; TIME PCR ASSAY; DNA; BLOOD;
D O I
10.1016/j.diagmicrobio.2016.07.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The choice of nucleic acids (NAs) extraction method for molecular diagnosis in microbiology is of major importance because of the low microbial load, different nature of microorganisms, and clinical specimens. The NA yield of different extraction methods has been mostly studied using spiked samples. However, information from real human clinical specimens is scarce. The purpose of this study was to compare the performance of a manual low-cost extraction method (Qiagen kit or salting-out extraction method) with the automated high-cost MagNAPure Compact method. According to cycle threshold values for different pathogens, MagNAPure is as efficient as Qiagen for NA extraction from noncomplex clinical specimens (nasopharyngeal swab, skin swab, plasma, respiratory specimens). In contrast, according to cycle threshold values for RNAseP, MagNAPure method may not be an appropriate method for NA extraction from blood. We believe that MagNAPure versatility reduced risk of cross-contamination and reduced hands-on time compensates its high cost (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:268 / 269
页数:2
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