首页> 美国卫生研究院文献>BioMed Research International >SNP Typing Using Multiplex Real-Time PCR Assay for Species Identification of Forensically Important Blowflies and Fleshflies Collected in South Korea (Diptera: Calliphoridae and Sarcophagidae)
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SNP Typing Using Multiplex Real-Time PCR Assay for Species Identification of Forensically Important Blowflies and Fleshflies Collected in South Korea (Diptera: Calliphoridae and Sarcophagidae)

机译:使用多重实时PCR分析进行SNP分型,以鉴定在韩国收集的法医重要的蝇类和肉蝇(双翅目:Calliphoridae和Sarcophagidae)

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摘要

Medicolegal entomology—a subfield of forensic entomology—is mainly used in medicolegal investigations to estimate the postmortem interval (PMI). The minimum PMI of a corpse invaded by necrophagous immature insects can be estimated because the PMI is near to or earlier than the oviposition time of the larvae that hatched and fed on the corpse. As the growth speeds of larvae differ depending on temperature and species, species-specific growth data are used to estimate the minimum PMI. While morphological identification of adult necrophagous flies can be done by a well-trained entomologist, identification of larvae is relatively difficult. Larvae can only be identified up to the family level and developmental stage by observing the posterior spiracles. For these reasons, the molecular biology method of DNA barcoding has been developed. DNA barcoding that targets the mitochondrial cytochrome c oxidase subunit I (COI) gene is commonly used. COI sequences are currently acquired using polymerase chain reaction (PCR) and Sanger sequencing, which are too time-consuming and complex for practical use in medicolegal investigations. To compensate for these limitations and facilitate the use of entomology for medicolegal investigation, we designed a multiplex real-time PCR system to identify nineteen forensically important species of Calliphoridae and Sarcophagidae flies collected in South Korea. In contrast to the Sanger nucleotide sequencing process, this technology only requires a one-step real-time PCR with melt curve analysis of amplicons generated by primers targeting species-specific single nucleotide polymorphisms (SNPs). Multiplex real-time PCR was performed for twelve species of Calliphoridae (four reactions) and for seven species of Sarcophagidae (three reactions). This assay is expected to make it easier and faster for investigating authorities to identify major species of necrophagous flies at beginning of investigation and to increase the utilization of entomological evidence in forensic investigations.
机译:法医昆虫学是法医昆虫学的一个子领域,主要在法医学研究中用于估计验尸间隔(PMI)。可以估计出由食虫性未成熟昆虫入侵的尸体的最小PMI,因为PMI接近或早于孵化并以尸体为食的幼虫的产卵时间。由于幼虫的生长速度因温度和物种而异,因此使用特定物种的生长数据来估计最小PMI。虽然可以由训练有素的昆虫学家完成对成年食虫蝇的形态学鉴定,但鉴定幼虫却相对困难。只能通过观察后气孔来确定幼虫直至家庭水平和发育阶段。由于这些原因,已经开发了DNA条形码的分子生物学方法。通常使用靶向线粒体细胞色素C氧化酶亚基I(COI)基因的DNA条形码。目前,COI序列是使用聚合酶链反应(PCR)和Sanger测序获得的,对于在法医学研究中的实际应用而言,它们既费时又复杂。为了弥补这些局限性并促进昆虫学在法医学研究中的应用,我们设计了一个多重实时PCR系统,以鉴定在韩国收集的十九种法医学上重要的Calliphoridae和Sarcophagidae蝇。与Sanger核苷酸测序过程相比,该技术仅需一步一步实时PCR,即可对目标物种特异性单核苷酸多态性(SNP)引物生成的扩增子进行熔解曲线分析。对十二种Calliphoridae(四个反应)和七种Sarcophagidae(三个反应)进行了多重实时PCR。预期这种分析将使调查机构在调查开始时更容易,更快地识别出食虫蝇的主要种类,并提高法医调查中昆虫学证据的利用率。

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