scholarly journals Identification of Forensically Important Calliphoridae and Sarcophagidae Species Collected in Korea Using SNaPshot Multiplex System Targeting the Cytochrome c Oxidase Subunit I Gene

2018 ◽  
Vol 2018 ◽  
pp. 1-9
Author(s):  
Ji Hye Park ◽  
Sang Eon Shin ◽  
Kwang Soo Ko ◽  
Seong Hwan Park

Estimation of postmortem interval (PMI) is paramount in modern forensic investigation. After the disappearance of the early postmortem phenomena conventionally used to estimate PMI, entomologic evidence provides important indicators for PMI estimation. The age of the oldest fly larvae or pupae can be estimated to pinpoint the time of oviposition, which is considered the minimum PMI (PMImin). The development rate of insects is usually temperature dependent and species specific. Therefore, species identification is mandatory for PMImin estimation using entomological evidence. The classical morphological identification method cannot be applied when specimens are damaged or have not yet matured. To overcome this limitation, some investigators employ molecular identification using mitochondrial cytochrome c oxidase subunit I (COI) nucleotide sequences. The molecular identification method commonly uses Sanger’s nucleotide sequencing and molecular phylogeny, which are complex and time consuming and constitute another obstacle for forensic investigators. In this study, instead of using conventional Sanger’s nucleotide sequencing, single-nucleotide polymorphisms (SNPs) in the COI gene region, which are unique between fly species, were selected and targeted for single-base extension (SBE) technology. These SNPs were genotyped using a SNaPshot® kit. Eleven Calliphoridae and seven Sarcophagidae species were covered. To validate this genotyping, fly DNA samples (103 adults, 84 larvae, and 4 pupae) previously confirmed by DNA barcoding were used. This method worked quickly with minimal DNA, providing a potential alternative to conventional DNA barcoding. Consisting of only a few simple electropherogram peaks, the results were more straightforward compared with those of the conventional DNA barcoding produced by Sanger’s nucleotide sequencing.

2011 ◽  
Vol 11 (6) ◽  
pp. 1002-1011 ◽  
Author(s):  
GREGG P. ROBIDEAU ◽  
ARTHUR W. A. M. De COCK ◽  
MICHAEL D. COFFEY ◽  
HERMANN VOGLMAYR ◽  
HENK BROUWER ◽  
...  

Acta Tropica ◽  
2016 ◽  
Vol 161 ◽  
pp. 1-7 ◽  
Author(s):  
Kanapathy Gajapathy ◽  
Tharmatha Tharmasegaram ◽  
Thampoe Eswaramohan ◽  
Lalanthika B.S.L. Peries ◽  
Raveendra Jayanetti ◽  
...  

2019 ◽  
Vol 65 (1) ◽  
pp. 283-287 ◽  
Author(s):  
Hari Jang ◽  
Sang Eon Shin ◽  
Kyu Jin Youm ◽  
Mustafa Zafer Karagozlu ◽  
Chang Bae Kim ◽  
...  

Zootaxa ◽  
2021 ◽  
Vol 4927 (1) ◽  
pp. 1-8
Author(s):  
PARASKEVA MICHALOVA ◽  
VALERIA LENCIONI ◽  
MOMCHIL NENOV ◽  
SVETOSLAV NIKOLOV

DNA barcoding based on a fragment of mitochondrial Cytochrome C Oxidase subunit 1 gene (COI) was applied to the two chironomids Clunio balticus Heimbach (690 base pairs) and C. ponticus Michailova (691 base pairs). The two species differed by one deletion in the nucleotide sequence Adenine. However, the 658-nucleotide long sequences of DNA from the mitochondrial Cytochrome C Oxidase subunit 1 gene (COI) of C. balticus and C. ponticus were identical upon comparison. Further, they compared with homologous sequences for C. marinus Holiday and C. tsushimensis Tokunaga from the Barcode of Life (BOLD) database and the results plotted as a weighted graph, where C. tsushimensis, C. marinus and C. balticus C. ponticus formed three almost equidistant groups. From this, we established that the genetic distance between the respective COI sequences of C. balticus and C. ponticus is minimal, indicating a close relationship between the species indicative of recent common origin. However, the comparative analysis between C. tsushimensis, C. marinus, C. balticus and C. ponticus showed a wider divergence in their respective nucleotide sequences. Overall, our results emphasized that the COI region does not work well as a DNA barcode to identify species within the Clunio genus. Either longer sequences or a multifaceted methodological approach, including morphology, cytogenetic and ecology is needed to distinguish some members of Clunio genus.  


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