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评估从艰难梭菌中提取 DNA 和 RNA 的商用试剂盒。

Evaluation of commercial kits for extraction of DNA and RNA from Clostridium difficile.

机构信息

Department of Pathobiology, Ontario Veterinary College, University of Guelph, 50 Stone Road, Guelph, Ontario, Canada N1G 2W1.

出版信息

Anaerobe. 2012 Dec;18(6):608-13. doi: 10.1016/j.anaerobe.2012.10.003. Epub 2012 Nov 2.

DOI:10.1016/j.anaerobe.2012.10.003
PMID:23128271
Abstract

Commercial nucleic acid extraction kits are a cost effective, efficient and convenient way to isolate DNA and RNA from bacteria. Despite the increasing importance of the gastrointestinal pathogen, Clostridium difficile, and the increased use of nucleic acids in its identification, characterization, and investigation of virulence factors, no standardized or recommended methods for nucleic acid isolation exist. Here, we sought to evaluate 4 commercial DNA extraction kits and 3 commercial RNA extraction kits assessing cost, labor intensity, purity, quantity and quality of nucleic acid preparations. The DNA extraction kits produced a range of concentrations (20.9-546 ng/ml) and A(260/280) ratios (1.92-2.11). All kits were suitable for DNA extraction with the exception of the Roche MagNA pure LC DNA isolation kit III which produced DNA of high yield but with substantial shearing, but that did not affect downstream PCR amplifications. For RNA extraction, the Qiagen RNeasy mini kit stood out producing preparations of consistently higher concentrations and higher RNA integrity numbers (RIN). The Roche MagNA pure LC RNA isolation kit produced preparations that could not be properly assigned RINs due to a failure to remove small RNAs which were interpreted as degradation. Good DNA and RNA yield are critical but methods are often overlooked. This study highlights the potential for critical variation between established commercial systems and the need for assessment of any extraction methods that are used.

摘要

商业核酸提取试剂盒是从细菌中分离 DNA 和 RNA 的一种经济有效、高效且方便的方法。尽管胃肠道病原体艰难梭菌的重要性日益增加,并且越来越多地使用核酸来鉴定、表征和研究其毒力因子,但目前还没有标准化或推荐的核酸分离方法。在这里,我们评估了 4 种商用 DNA 提取试剂盒和 3 种商用 RNA 提取试剂盒,评估了成本、劳动强度、纯度、核酸提取的产量和质量。DNA 提取试剂盒产生了一系列浓度(20.9-546ng/ml)和 A(260/280)比值(1.92-2.11)。除 Roche MagNA pure LC DNA 分离试剂盒 III 外,所有试剂盒均适用于 DNA 提取,该试剂盒虽然产生了高产量的 DNA,但 DNA 严重断裂,但不影响下游 PCR 扩增。对于 RNA 提取,Qiagen RNeasy mini 试剂盒脱颖而出,产生的浓度始终更高,RNA 完整性数量(RIN)更高。Roche MagNA pure LC RNA 分离试剂盒产生的 RNA 不能正确分配 RIN,因为未能去除被解释为降解的小 RNA。良好的 DNA 和 RNA 产量是至关重要的,但方法往往被忽视。本研究强调了现有商业系统之间可能存在的重大差异,以及需要评估任何使用的提取方法。

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