Thoendel Matthew, Jeraldo Patricio, Greenwood-Quaintance Kerryl E, Yao Janet, Chia Nicholas, Hanssen Arlen D, Abdel Matthew P, Patel Robin
Division of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Department of Surgery, Mayo Clinic, Rochester, Minnesota, USA.
J Clin Microbiol. 2017 Jun;55(6):1789-1801. doi: 10.1128/JCM.02402-16. Epub 2017 Mar 29.
Whole-genome amplification (WGA) is a useful tool for amplification of very small quantities of DNA for many uses, including metagenomic shotgun sequencing for infection diagnosis. Depending on the application, background DNA from WGA kits can be problematic. Three WGA kits were tested for their utility in a metagenomics approach to identify the pathogens in sonicate fluid comprised of biofilms and other materials dislodged from the surfaces of explanted prosthetic joints using sonication. The Illustra V2 Genomiphi, Illustra single cell Genomiphi, and Qiagen REPLI-g single cell kits were used to test identical sonicate fluid samples. Variations in the number of background reads, the genera identified in the background, and the number of reads from known pathogens known to be present in the samples were observed between kits. These results were then compared to those obtained with a library preparation without prior WGA using an NEBNext Ultra II paired-end kit, which requires a very small amount of input DNA. This approach also resulted in the presence of contaminant bacterial DNA and yielded fewer reads from the known pathogens. These findings highlight the impact that WGA kit selection can have on metagenomic analysis of low-biomass samples and the importance of the careful selection and consideration of the implications of using these tools.
全基因组扩增(WGA)是一种用于扩增极少量DNA的有用工具,可用于多种用途,包括用于感染诊断的宏基因组鸟枪法测序。根据应用的不同,WGA试剂盒中的背景DNA可能会带来问题。测试了三种WGA试剂盒在宏基因组学方法中的效用,该方法用于鉴定通过超声处理从植入的人工关节表面去除的生物膜和其他物质组成的超声处理液中的病原体。使用Illustra V2 Genomiphi、Illustra单细胞Genomiphi和Qiagen REPLI-g单细胞试剂盒对相同的超声处理液样本进行测试。在不同试剂盒之间观察到背景读数数量、背景中鉴定出的属以及样本中已知存在的已知病原体的读数数量存在差异。然后将这些结果与使用NEBNext Ultra II双端试剂盒(该试剂盒需要极少量的输入DNA)在不进行预先WGA的情况下进行文库制备所获得的结果进行比较。这种方法也导致了污染细菌DNA的存在,并且已知病原体的读数较少。这些发现突出了WGA试剂盒的选择对低生物量样本宏基因组分析的影响,以及谨慎选择和考虑使用这些工具的影响的重要性。