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评估用于性侵犯调查的新型和传统细胞分离技术。

Evaluating novel and conventional cell-separation techniques for sexual assault investigations.

作者信息

Schulte Janine, Egger Simon, Kron Sarah, Scheurer Eva, Schulz Iris

机构信息

Institute of Forensic Medicine, University Basel, Basel, Switzerland.

出版信息

J Forensic Sci. 2025 Sep;70(5):1704-1720. doi: 10.1111/1556-4029.70131. Epub 2025 Jul 11.

Abstract

Biological evidence from sexual assaults frequently includes few male cells (i.e., spermatozoa) and numerous female cells (i.e., epithelial cells). In practice, their genetic analysis typically involves separating the victim's cells from the perpetrator's sperm using conventional differential extraction or advanced cell enrichment/capturing techniques. A descriptive study on simulated sexual assault samples was carried out by the recruitment of 10 heterosexual, monogamous couples. Post-coital swabs were collected before and after consensual sexual intercourse, with a sampling period of up to 96 h, and subjected to analysis to detect, quantify, and genotype adhering sperm by three distinct cell-separation techniques: differential extraction, laser capture microdissection, and DEPArray™. Methods differed in sperm detection and genotyping efficacy, while foreign DNA was identifiable up to 96 h. Time since intercourse and individuals were statistically significant factors (p ≤ 0.05) on male DNA yields, while hygienic behavior was not. Prior sperm enrichment was pivotal for cell capture technologies to counteract the abundance of epithelial cells, achieved by a prior mild digestion step for laser microdissection. Evaluating the advantages and disadvantages of standard and advanced methods provided a novel, comprehensive understanding of their merits, postulating that modern applications can assist conventional ones in challenging crime samples.

摘要

性侵犯的生物学证据通常包括少量男性细胞(即精子)和大量女性细胞(即上皮细胞)。在实际操作中,对它们的基因分析通常涉及使用传统的差异提取法或先进的细胞富集/捕获技术,将受害者的细胞与犯罪者的精子分离。通过招募10对异性恋、一夫一妻制的夫妇,对模拟性侵犯样本进行了一项描述性研究。在双方自愿性交前后采集性交后拭子,采样期长达96小时,并采用三种不同的细胞分离技术:差异提取、激光捕获显微切割和DEPArray™,对附着的精子进行检测、定量和基因分型分析。不同方法在精子检测和基因分型效率上存在差异,而外来DNA在长达96小时内均可识别。性交后的时间和个体是影响男性DNA产量的统计学显著因素(p≤0.05),而卫生行为则不是。对于细胞捕获技术而言,预先进行精子富集对于抵消上皮细胞的大量存在至关重要,这可通过激光显微切割前的轻度消化步骤来实现。评估标准方法和先进方法的优缺点,能让人对它们的优点有全新的全面理解,推测现代应用可在处理具有挑战性的犯罪样本时辅助传统方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d7c/12424101/f120d77c0f1d/JFO-70-1704-g005.jpg

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