Dargay Amanda, Roy Reena
The Pennsylvania State University, Forensic Science Program, Eberly College of Science, University Park, PA 16802, USA.
The Pennsylvania State University, Forensic Science Program, Eberly College of Science, University Park, PA 16802, USA.
J Forensic Leg Med. 2016 Apr;39:50-60. doi: 10.1016/j.jflm.2016.01.012. Epub 2016 Jan 25.
Body fluids detected on commonly found crime scene substrates require extraction, purification and quantitation of DNA prior to amplification and generation of short tandem repeat (STR) DNA profiles. In this research Y-STR profiles were generated via direct amplification of blood and saliva deposited on 12 different substrates. These included cigarette butts, straws, grass, leaves, woodchips and seven different types of fabric. After depositing either 0.1 μL of blood or 0.5 μL of saliva, each substrate containing the dry body fluid stain was punched using a Harris 1.2 mm micro-punch. Each of these punched substrates, a total of 720 samples, containing minute amount of blood or saliva was either amplified directly without any pre-treatment, or was treated with one of the four washing reagents or buffer. In each of these five experimental groups the substrates containing the body fluid remained in the amplification reagent during the thermal cycling process. Each sample was amplified with the three direct Y-STR amplification kits; AmpFℓSTR(®) Yfiler(®) Direct, Yfiler(®) Plus Amplification Kits and the PowerPlex(®) Y23 System. Complete and concordant Y-STR profiles were successfully obtained from most of these 12 challenging crime scene objects when the stains were analyzed by at least one of the five experimental groups. The reagents and buffer were interchangeable among the three amplification kits, however, pre-treatment with these solutions did not appear to enhance the quality or the number of the full profiles generated with direct amplification. This study demonstrates that blood and saliva deposited on these simulated crime scene objects can be amplified directly.
在常见犯罪现场基质上检测到的体液,在进行短串联重复序列(STR)DNA图谱扩增和生成之前,需要对DNA进行提取、纯化和定量。在本研究中,通过直接扩增沉积在12种不同基质上的血液和唾液来生成Y-STR图谱。这些基质包括烟头、吸管、草、树叶、木屑和七种不同类型的织物。在沉积0.1μL血液或0.5μL唾液后,使用哈里斯1.2mm微型打孔器对每个含有干燥体液污渍的基质进行打孔。这些打孔后的基质,总共720个样本,含有微量血液或唾液,要么未经任何预处理直接扩增,要么用四种洗涤试剂或缓冲液之一进行处理。在这五个实验组中的每一组中,含有体液的基质在热循环过程中都留在扩增试剂中。每个样本都用三种直接Y-STR扩增试剂盒进行扩增;AmpFℓSTR(®) Yfiler(®) Direct、Yfiler(®) Plus扩增试剂盒和PowerPlex(®) Y23系统。当通过五个实验组中的至少一组对污渍进行分析时,在这12种具有挑战性的犯罪现场物体中的大多数上成功获得了完整且一致的Y-STR图谱。这三种扩增试剂盒中的试剂和缓冲液是可互换的,然而,用这些溶液进行预处理似乎并没有提高直接扩增产生的完整图谱的质量或数量。本研究表明,沉积在这些模拟犯罪现场物体上的血液和唾液可以直接扩增。