Department of Biomedical, Metabolic and Neural Sciences, Institute of Legal Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Department of Mathematics, University of Bologna, Bologna, Italy.
Int J Legal Med. 2019 Nov;133(6):1743-1750. doi: 10.1007/s00414-019-02146-6. Epub 2019 Aug 28.
Storage conditions influence the integrity of the recoverable DNA from forensic evidence in terms of yield and quality. FTA cards are widely used in the forensic practice as their chemically treated matrix provides protection from the moment of collection to the point of analysis with current STR typing technology. In this study, we assess the recoverability and the integrity of DNA from 11-year-old saliva on FTA cards using a forensic quantitative real-time polymerase chain reaction (qPCR) commercial assay. The quality after long-term storage was investigated in order to evaluate if the FTA device could assure enough stability over time, applying some internally validated quality criteria of the STR profile. Furthermore, we used a 3D interpolation model to combine the quantitative and qualitative data from qPCR to calculate the minimum optimal DNA input (MODI) to add to the downstream PCR reaction based on the quantitative and qualitative data of a sample. According to our results, when saliva sample is properly transferred onto FTA cards and then correctly stored according to the manufacturer's instructions, it is possible to recover sufficient amounts of DNA for human identification even after more than a decade of storage at ambient temperature. Degradation affected the quality of results especially when the Degradation Index exceeds the value of 2.12, requiring modifications of the standard internal workflow to improve the genotyping quality. Above this value, the application of a "corrective factor" to the PCR normalization process was necessary in order to adjust the recommended manufacturer's PCR DNA input taking into account the degradation level. Our results demonstrated the importance to consider in predictive terms the parameters obtained with the real-time quantification assay, both in terms of quantity (DNA concentration) and of quality (DI, inhibition). Informatics predictive tools including qPCR data together with the variables of storage duration and conditions should be developed in order to optimize the DNA analysis process.
储存条件会影响法医证据中可回收 DNA 的完整性,包括产量和质量。FTA 卡广泛应用于法医实践中,其化学处理的基质在采集到分析的过程中为当前的 STR 分型技术提供了保护。在这项研究中,我们使用法医定量实时聚合酶链反应 (qPCR) 商业检测试剂盒评估了 11 年前唾液在 FTA 卡上的可回收性和完整性。为了评估 FTA 设备是否能够随着时间的推移保持足够的稳定性,我们研究了长期储存后的质量,应用 STR 谱内部验证的一些质量标准。此外,我们使用 3D 插值模型将 qPCR 的定量和定性数据结合起来,根据样本的定量和定性数据计算添加到下游 PCR 反应中的最小最优 DNA 输入 (MODI)。根据我们的结果,只要唾液样本正确转移到 FTA 卡上,并按照制造商的说明正确储存,即使在室温下储存超过十年,也可以从 DNA 中提取出足够的用于人类识别的 DNA。降解会影响结果的质量,尤其是当降解指数超过 2.12 时,需要修改标准内部工作流程以提高基因分型质量。超过该值时,需要对 PCR 归一化过程应用“校正因子”,以根据降解水平调整制造商推荐的 PCR DNA 输入。我们的结果表明,必须根据实时定量检测获得的参数,从数量(DNA 浓度)和质量(DI、抑制)两个方面考虑预测因素。为了优化 DNA 分析过程,应该开发包括 qPCR 数据在内的预测工具以及储存时间和条件等变量。