Kitayama Tetsushi, Fukagawa Takashi, Watahiki Haruhiko, Mita Yusuke, Fujii Koji, Unuma Kana, Sakurada Koichi, Uemura Koichi, Sekiguchi Kazumasa, Mizuno Natsuko
National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba 277-0882, Japan.
National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba 277-0882, Japan.
Leg Med (Tokyo). 2020 Sep;46:101713. doi: 10.1016/j.legalmed.2020.101713. Epub 2020 May 6.
An evaluation of a Rapid DNA system was performed using buccal swab samples and mock Disaster Victim Identification (DVI) samples collected postmortem. The allelic ladder success rate was 90% and samples analyzed simultaneously with this allelic ladder were used for further analysis. Sample success rate of the Rapid DNA system for buccal swab samples, and blood and muscle DVI samples were calculated. Success rates of buccal swab samples were 100% and 75% using cassettes preloaded with all reagents suitable for high- and low-DNA content samples, respectively. Success rates of fresh DVI samples were 80% to 100%. Success rates of putrefied DVI samples varied widely between 0% and 20% and 50% to 80% depending on cassette and sample types. Conventional DNA analysis was performed for comparison with the results of the Rapid DNA system. DNA quantity and degradation of human DNA were measured using quantitative polymerase chain reaction. DVI samples that yielded more than 1 ng/µL of DNA when extracted with conventional protocols were suitable for analysis using cassettes for both high- and low-DNA content samples. DVI samples with less than 0.1 ng/µL of DNA were suitable only for analysis using cassettes for low-DNA content samples. All alleles called and exported by the Expert system software implemented in the Rapid DNA system were concordant with allele calls made by conventional capillary electrophoresis DNA analysis.
使用口腔拭子样本和死后采集的模拟灾难受害者身份识别(DVI)样本对快速DNA系统进行了评估。等位基因阶梯成功率为90%,与该等位基因阶梯同时分析的样本用于进一步分析。计算了快速DNA系统对口腔拭子样本以及血液和肌肉DVI样本的样本成功率。使用预装有适用于高DNA含量和低DNA含量样本的所有试剂的试剂盒时,口腔拭子样本的成功率分别为100%和75%。新鲜DVI样本的成功率为80%至100%。腐败DVI样本的成功率因试剂盒和样本类型而异,在0%至20%和50%至80%之间波动很大。进行了常规DNA分析以与快速DNA系统的结果进行比较。使用定量聚合酶链反应测量人类DNA的量和降解情况。当用常规方法提取时产生超过1 ng/µL DNA的DVI样本适用于使用适用于高DNA含量和低DNA含量样本的试剂盒进行分析。DNA含量低于0.1 ng/µL的DVI样本仅适用于使用适用于低DNA含量样本的试剂盒进行分析。快速DNA系统中实施的专家系统软件调用和输出的所有等位基因与常规毛细管电泳DNA分析得出的等位基因调用结果一致。