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用于大规模死亡事件后基于 DNA 的受害者识别的常温下长期组织保存。

Long-Term Tissue Preservation at Ambient Temperature for Post-Mass Fatality Incident DNA-Based Victim Identification.

机构信息

DNA Profiling Laboratory, Biology Division, Health Sciences Authority, 11 Outram Road, Singapore 169078, Singapore.

出版信息

Genes (Basel). 2024 Mar 19;15(3):373. doi: 10.3390/genes15030373.

DOI:10.3390/genes15030373
PMID:38540432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10970238/
Abstract

In a mass fatality incident (MFI), effective preservation of tissue samples is the cornerstone for downstream DNA-based identification of victims. This is commonly achieved through freezing of tissue samples excised from bodies/fragmented remains which may be buried or stored in refrigerated containers. This may, however, not be possible depending on the nature of the MFI; in particular, during armed conflict/war where extended periods of electrical outages would be expected. The present study compared the effectiveness of long-term tissue preservation at ambient temperatures using two commercial products (non-iodized kitchen salt and a 40% alcoholic beverage) against a chemical preservative (Allprotect™ Tissue Reagent (Qiagen, Germantown, MD, USA)) and freezing at -20 °C. Bovine muscle tissue, used as a proxy for human tissue, was treated with the four preservation methods and sampled at six different time-points over a 24-month period. All four methods were able to preserve the bovine tissue, generally yielding STR-PCR (Short Tandem Repeat-Polymerase Chain Reaction) amplicons > 200 bp in size even at the end of 24 months. Gel electrophoresis, however, indicated that salt was more effective in preserving DNA integrity with high-molecular-weight DNA clearly visible as compared to the low-molecular-weight DNA smears observed in the other methods. This study also proposes a simple process for the rapid and low-cost preservation of tissue samples for long-term storage at ambient temperatures in support of post-incident victim identification efforts.

摘要

在大规模死亡事件(MFI)中,有效地保存组织样本是下游基于 DNA 的受害者识别的基石。这通常通过冷冻从尸体/碎尸中切除的组织样本来实现,这些组织样本可能被埋在地下或储存在冷藏容器中。然而,这可能并不可能,具体取决于 MFI 的性质;特别是在武装冲突/战争期间,预计会出现长时间的停电。本研究比较了在环境温度下使用两种商业产品(未碘化的厨房盐和 40%酒精饮料)以及在-20°C 下冷冻对长期组织保存的效果,这两种商业产品分别是商业产品(非碘化厨房盐和 40%酒精饮料)和化学防腐剂(Allprotect™ Tissue Reagent(Qiagen,Germantown,MD,USA))。使用这四种保存方法处理牛肌肉组织(用作人体组织的替代品),并在 24 个月的时间内分六个不同时间点进行采样。这四种方法都能够保存牛组织,通常在 24 个月结束时仍能产生大小>200bp 的 STR-PCR(短串联重复-聚合酶链反应)扩增子。然而,凝胶电泳表明,盐在保存 DNA 完整性方面更有效,与其他方法中观察到的低分子量 DNA 涂片相比,高分子量 DNA 清晰可见。本研究还提出了一种简单的方法,用于快速、低成本地保存组织样本,以便在环境温度下长期储存,以支持事后受害者识别工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/b7ac4b91845f/genes-15-00373-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/cace69c270a9/genes-15-00373-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/2e537167ff02/genes-15-00373-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/8a64d13bedea/genes-15-00373-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/062b2d046438/genes-15-00373-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/b7ac4b91845f/genes-15-00373-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/cace69c270a9/genes-15-00373-g0A1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/2e537167ff02/genes-15-00373-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/8a64d13bedea/genes-15-00373-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/062b2d046438/genes-15-00373-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/974b/10970238/b7ac4b91845f/genes-15-00373-g004.jpg

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