变异链球菌在法医牙学分析中的限制性片段长度多态性

Q2 Agricultural and Biological Sciences Bioscience Horizons Pub Date : 2010-06-01 DOI:10.1093/BIOHORIZONS/HZQ021
Paul S Spradbery
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引用次数: 7

摘要

人类互相咬人的频率惊人。这种伤害可能导致法医调查,并最终导致刑事起诉。咬痕分析技术包括牙齿测量,ABO血清分型和DNA分析,没有一种是绝对正确的。对其他技术的研究将是有利的。咬人还包括细菌从牙齿转移到皮肤,反之亦然。在前牙上发现的主要物种是变形链球菌,它在人类中很普遍。本研究的目的是在法医牙科学的背景下,确定这种普遍存在的口腔细菌的染色体DNA谱在高加索人样本中是否会有显著差异(P = 0.05)。因此,如果存在足够的歧视性力量,该技术可被认为对法医调查有用。从10例成人的下门牙中回收了口腔液。样品选择性地使用mitis salivarius杆菌肽琼脂进行培养,并进行微生物学试验以进行鉴别。这些包括菌落形态的视觉评估,革兰氏染色和显微镜分析,然后是过氧化氢酶的化学测试。从传代培养细胞中提取染色体DNA,琼脂糖凝胶电泳分离,紫外透照观察。DNA的存在得到了证实。随后,使用27个正向引物和1492个反向引物,通过聚合酶链反应扩增16S核糖体RNA基因。扩增子像之前一样被分解和观察。扩增产物用限制性内切酶HaeIII孵育消化,聚丙烯酰胺凝胶电泳分离并观察。凝胶剖面采用线性回归分析计算限制性片段长度。对排序数据进行Kruskal-Wallis(方差分析)检验(H = 8.161, df = 9, P = 0.518)。因此,零假设(无主体间变异)被接受。然而,除了两个侧面外,所有侧面都被证明是独特的。为口腔细菌基因分型在法医咬痕案件中的应用提供了原理证明。
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Restriction fragment length polymorphisms of mutans streptococci in forensic odontological analysis
Humans bite each other with alarming frequency. Such injuries can result in forensic investigation and, ultimately, criminal prosecution. Bite mark analysis techniques include odontometric measurement, ABO serotyping and DNA profiling, none of which is infallible. Research into additional techniques would be advantageous. Biting involves, also, bacterial transfer from teeth to skin and vice versa. The principal species found on anterior teeth is Streptococcus mutans, which is universal among humans. The aim of this research was to establish, in the context of forensic odontology, whether chromosomal DNA profiles of this ubiquitous oral bacterium would vary significantly among a sample of Caucasian individuals (P = 0.05). Hence, if sufficient discriminatory power were present, the technique could be deemed useful to forensic investigation. Oral fluid was recovered from the lower incisors of 10 adults. Samples were cultured selectively using mitis salivarius bacitracin agar and microbiological tests carried out for the purpose of differential identification. These included visual assessment of colony morphology, Gram staining and microscopic analysis, followed by chemical testing for the enzyme catalase. Chromosomal DNA was extracted from subcultured cells, resolved by agarose gel electrophoresis and viewed using ultraviolet transillumination. The presence of DNA was confirmed. Subsequently, the 16S ribosomal RNA gene was amplified by polymerase chain reaction using specific 27 forward and 1492 reverse primers. Amplicons were resolved and viewed as previously. Amplified products were digested by incubation with restriction endonuclease HaeIII, resolved by polyacrylamide gel electrophoresis and viewed. Linear regression analysis of gel profiles was used to calculate restriction fragment lengths. A Kruskal-Wallis (analysis of variance) test was performed on ranked data (H = 8.161, df = 9, P = 0.518). Consequently, the null hypothesis (no inter-subject variation) was accepted. However, all but two profiles were proved to be unique. Proof of principle was provided regarding the application of oral bacterial genotyping to forensic bite mark cases.
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Bioscience Horizons
Bioscience Horizons Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
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