Towards the identification of body fluids using RT-LAMP isothermal amplification coupled with CRISPR-Cas12a

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY
Courtney R.H. Lynch , Olivia L. Martin , Craig Billington , Rachel Fleming
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引用次数: 0

Abstract

While often necessary in sexual assault cases, confirmatory identification of body fluids can be a lengthy and/or costly process. In particular, the detection of vaginal fluid and menstrual fluid in forensic casework is limited to endpoint reverse-transcription PCR to detect fluid-specific messenger RNA (mRNA) markers as there are no robust chemical or enzymatic techniques available for these fluids. Similarly, testing for rectal mucosa is not possible with standard methods, the presence of which would provide probative value in cases of alleged anal penetration, although mRNA-based markers have recently been described. Reverse-transcription loop-mediated isothermal amplification (RT-LAMP) is an alternative technique that enables detection of mRNA at a single temperature (usually 60–65℃) for 10–30 minutes and has comparable sensitivity to PCR. We describe the coupling of RT-LAMP amplification (60℃ for 30 minutes) with CRISPR-mediated fluorescent detection of the body fluid specific mRNA markers MMP3 (menstrual fluid), CYP2B7P (vaginal material), TNP1 (spermatozoa), KLK2 (semen), and MUC12 (rectal mucosa). Following temperature optimization and final selection of RT-LAMP-CRISPR assays, their specificity across circulatory blood, buccal, menstrual fluid, vaginal material, semen, and rectal mucosa was assessed. Most assays were specific for their intended target body fluid, although MMP3 and CYP2B7P were detected in some rectal mucosa samples, the latter of which has been observed previously in the literature. A preliminary sensitivity assessment in target fluids was determined by a dilution series over six logs of RNA input. A range of assay approaches were investigated to develop a protocol suitable for use in a forensic screening laboratory. This included the determination of fluorescent assay results by eye, use of lyophilised reagents, and RT-LAMP and CRISPR reactions undertaken in one-tube in a lower resource setting.
利用 RT-LAMP 等温扩增技术和 CRISPR-Cas12a 对体液进行鉴定。
虽然在性侵犯案件中往往有必要对体液进行确认鉴定,但这一过程可能会很漫长和/或昂贵。特别是,在法医案件工作中,对阴道分泌物和月经分泌物的检测仅限于终端反转录聚合酶链反应,以检测分泌物特异性信使核糖核酸(mRNA)标记,因为对这些分泌物没有可靠的化学或酶技术可用。同样,标准方法也无法检测直肠粘膜,尽管最近描述了基于 mRNA 的标记物,但直肠粘膜的存在可为指称的肛门插入案件提供证据价值。反转录环介导等温扩增(RT-LAMP)是一种替代技术,可在 10-30 分钟的单一温度(通常为 60-65℃)下检测 mRNA,灵敏度与 PCR 相当。我们介绍了 RT-LAMP 扩增(60℃ 30 分钟)与 CRISPR 介导的体液特异性 mRNA 标记 MMP3(月经液)、CYP2B7P(阴道分泌物)、TNP1(精子)、KLK2(精液)和 MUC12(直肠粘膜)的荧光检测。在对温度进行优化并最终选定 RT-LAMP-CRISPR 检测方法后,对其在循环血、口腔、月经液、阴道分泌物、精液和直肠粘膜中的特异性进行了评估。虽然在一些直肠粘膜样本中检测到了 MMP3 和 CYP2B7P,但大多数检测方法对其目标体液都具有特异性,后者以前在文献中也曾出现过。对目标体液的初步灵敏度评估是通过六对数 RNA 输入稀释系列确定的。对一系列检测方法进行了研究,以制定适合法医筛查实验室使用的方案。这包括用肉眼确定荧光检测结果、使用冻干试剂以及在资源较少的环境中以单管方式进行 RT-LAMP 和 CRISPR 反应。
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来源期刊
CiteScore
7.50
自引率
32.30%
发文量
132
审稿时长
11.3 weeks
期刊介绍: Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts. The scope of the journal includes: Forensic applications of human polymorphism. Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies. Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms. Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications. Non-human DNA polymorphisms for crime scene investigation. Population genetics of human polymorphisms of forensic interest. Population data, especially from DNA polymorphisms of interest for the solution of forensic problems. DNA typing methodologies and strategies. Biostatistical methods in forensic genetics. Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches. Standards in forensic genetics. Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards. Quality control. Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies. Criminal DNA databases. Technical, legal and statistical issues. General ethical and legal issues related to forensic genetics.
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