Griffiths Lisa J, Anyim Martin, Doffman Sarah R, Wilks Mark, Millar Michael R, Agrawal Samir G
Department of Microbiology, Barts and The London NHS Trust, Royal London Hospital, London, UK.
Department of Respiratory Medicine, Barts and The London NHS Trust, St Bartholomew's Hospital, London.
J Med Microbiol. 2006 Sep;55(Pt 9):1187-1191. doi: 10.1099/jmm.0.46510-0.
Newer methods such as PCR are being investigated in order to improve the diagnosis of invasive aspergillosis. One of the major obstacles to using PCR to diagnose aspergillosis is a reliable, simple method for extraction of the fungal DNA. The presence of a complex, sturdy cell wall that is resistant to lysis impairs extraction of the DNA by conventional methods employed for bacteria. Numerous fungal DNA extraction protocols have been described in the literature. However, these methods are time-consuming, require a high level of skill and may not be suitable for use as a routine diagnostic technique. Here, a number of extraction methods were compared: a freeze-thaw method, a freeze-boil method, enzyme extraction and a bead-beating method using Mini-BeadBeater-8. The quality and quantity of the DNA extracted was compared using real-time PCR. It was found that the use of a bead-beating method followed by extraction with AL buffer (Qiagen) was the most successful extraction technique, giving the greatest yield of DNA, and was also the least time-consuming method assessed.
为了改进侵袭性曲霉病的诊断,正在研究诸如PCR等更新的方法。使用PCR诊断曲霉病的主要障碍之一是一种可靠、简单的真菌DNA提取方法。真菌具有复杂、坚固且抗裂解的细胞壁,这使得采用用于细菌的传统方法提取DNA受到损害。文献中已描述了许多真菌DNA提取方案。然而,这些方法耗时、需要高水平的技能,并且可能不适合用作常规诊断技术。在此,比较了多种提取方法:冻融法、冻煮法、酶提取法以及使用Mini-BeadBeater-8的珠磨法。使用实时PCR比较了所提取DNA的质量和数量。结果发现,采用珠磨法然后用AL缓冲液(Qiagen)提取是最成功的提取技术,DNA产量最高,并且也是所评估的最省时的方法。