Department of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
MicroGEM International, 705D Dale Ave, Charlottesville, VA, 22904, USA.
Forensic Sci Int Genet. 2019 Jul;41:42-49. doi: 10.1016/j.fsigen.2019.03.012. Epub 2019 Mar 23.
We report the successful separation of sperm cells from a relevant composition of mock sexual assault samples using a novel acoustic differential extraction (ADE) technology. A multi-layer microfluidic device fabricated in a non-photolithographic process from glass and polydimethylsiloxane (PDMS) was capable of interfacing with custom-built instrumentation to exploit a standing acoustic wave for the trapping of individual sperm cells in a sample containing an abundance of epithelial cells. Samples were generated from buccal and vaginal swabs to mimic post-coital vaginal swabs, and processed through the ADE system followed by DNA extraction of the captured cells with amplification of DNA using a custom short tandem repeat (STR) chemistry. The prototype acoustic trapping technology was fully capable of isolating intact sperm cells from mock samples with disparate masses of male and female DNA. Other biological components were evaluated for adverse effects on sperm cell trapping, including blood, yeast, and bacteria (E. coli), and these had negligible effects on observed sperm cell trapping. Finally, we demonstrate the successful capture of sperm cells from mock samples containing a 40-fold excess in female epithelial cells over sperm cells. The effectiveness of sperm cell purification was ascertained with polymerase chain reaction (PCR) amplification of STR loci from the male fraction post separation with an 18-plex amplification kit, which resulted in male-only profiles.
我们报告了使用新型声学差分提取(ADE)技术,成功地从模拟性侵犯样本的相关成分中分离精子细胞。使用非光刻工艺从玻璃和聚二甲基硅氧烷(PDMS)制造的多层微流控装置能够与定制仪器接口,利用驻波捕获含有大量上皮细胞的样本中的单个精子细胞。样本取自颊拭子和阴道拭子,以模拟性交后的阴道拭子,并通过 ADE 系统进行处理,然后用捕获细胞的 DNA 提取,使用定制的短串联重复(STR)化学进行 DNA 扩增。原型声学捕获技术完全能够从模拟样本中分离出完整的精子细胞,这些模拟样本中男性和女性 DNA 的质量差异很大。还评估了其他生物成分对精子细胞捕获的不利影响,包括血液、酵母和细菌(大肠杆菌),这些成分对观察到的精子细胞捕获几乎没有影响。最后,我们展示了成功从含有 40 倍上皮细胞过量的模拟样本中捕获精子细胞。通过从分离后的男性部分进行 STR 基因座的聚合酶链反应(PCR)扩增,用 18 重扩增试剂盒确定了精子细胞的纯化效果,结果得到了仅男性的图谱。