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* These authors contributed equally
This article describes a protocol for fresh and old necrophilic fly DNA extraction using a modified common DNA extraction kit.
A total of five samples of Chrysomya megacephala samples - three fresh samples, one sample stored in alcohol for 2 years, and one sample stored in dry sealed storage for 2 years protected from light only - were selected to investigate whether a blood DNA extraction kit could extract DNA from necrophilous flies and to determine whether alcohol could prolong the preservation of necrophilous flies' DNA. First, the blood DNA extraction kit was used to extract DNA from their thorax tissues. Then, the DNA purity and concentration were examined using a microplate reader and a fluorometer. Finally, PCR amplification and electrophoresis of the extracted DNA were done with necrophilic fly-specific primers located in the mitochondrial CO I gene sequence. The results showed that the DNA purity of all samples was greater than 2.0. The DNA concentration was observed to be of the following order: fresh samples > alcohol-preserved old samples > untreated, old samples. All samples had specific electrophoretic bands after PCR amplification. In conclusion, a blood DNA extraction kit can be used to extract DNA from necrophilic flies successfully, and the DNA concentration of fresh fly samples is greater than that of old fly samples. The flies can be stored in alcohol for a long time.
The inference of the time of death has always been one of the key and difficult issues to be resolved in judicial practice. In the practice of forensic science, for a criminal case, determining postmortem interval plays a crucial role in deducing the time of the crime, locking in the suspect, and narrowing the scope of the investigation. Traditional methods of inferring the time of death are based primarily on early postmortem phenomena, which can generally only be used to infer the time of death within 24 h. However, the long time of death cannot be determined by postmortem phenomena. It is now generally recognized in the forensic science community that forensic ento....
NOTE: A total of five samples of C. megacephala samples were used in this protocol-three fresh samples (Fresh 1, Fresh 2, and Fresh 3), one sample stored in alcohol for 2 years (Old 1), and one sample stored in dry sealed storage for 2 years protected from light only (Old 2). Samples must be labeled according to the experimental requirements.
1. General sample storage and preparations
We used a microplate reader to measure the values of OD260 and OD280 of the extracted DNA solution and then obtained the OD260/OD280 values to evaluate the purity of the DNA. The OD260/OD280 of all fresh samples and old sample 1 was greater than 2. The OD260/OD280 of old sample 2 had a maximum value of 2.187 although the average was 1.753, and its three measurements fluctuated greatly due to the small (≤0.01) values of both its OD280 and OD280 (Table 1). Based on the value of OD260 obtained, we est.......
DNA extraction is the most critical link in the molecular identification of necrophilous flies, and its extraction method and the quality of the extracted DNA directly affect subsequent detection. In this experiment, we successfully extracted DNA from necrophilous flies by using a common blood kit, without the need to purchase a special insect DNA extraction kit, which makes insect DNA extraction easier to accomplish.
The surface of flies is rich in chitin, especially in the larval and pupal s.......
This work is supported by the National Natural Science Foundation of China (82060341,81560304) and by the Academician Innovation Platform Scientific Research Project of Hainan Province (YSPTZX202134).
....Name | Company | Catalog Number | Comments |
Buffer AE | Qiagen | 172026832 | DNA elution buffer |
Buffer AL | Qiagen | 172028374 | lysis buffer |
Buffer ATL | Qiagen | 172028162 | tissue lysis buffer |
Buffer AW1 | Qiagen | 172028760 | protein removal buffer |
Buffer AW2 | Qiagen | 57203108 | desalination buffer |
C1-J-2495 | Taihe Biotechnology | TW21109216 | forword primer |
C1-N-2800 | Taihe Biotechnology | TW21109217 | reverse primer |
D2000 DNA ladder | Real-Times(Beijing) Biotechnology | RTM415 | Measure the position of electrophoretic bands |
DNeasy Mini spin column | Qiagen | 166050343 | DNA adsorption column |
Dry Bath Incubator | Miulab | DKT200-2D | used for heating |
MIX-30S Mini Mixer | Miulab | MUC881206 | oscillatory action |
Proteinase K | Qiagen | 172026218 | Inactivation of intracellular nucleases and other proteins |
Qubit 3.0 Fluorometer | Thermo Fisher Scientific | 2321611188 | |
Speed Micro-Centrifuge | Scilogex | 9013001121 | centrifuge |
Standard#1 | Thermo Fisher Scientific | 2342797 | |
Standard#2 | Thermo Fisher Scientific | 2342797 | |
Tanon 3500R Gel Imager | Tanon | 16T5553R-455 | gel imaging |
Taq Mix Pro | Monad | 00007808-140534 | PCR Mix |
Taq Mix Pro | Monad | 00007808-140534 | PCR Mix |
Thermo Cycler | Zhuhai Hema | VRB020A | ordinary PCR |
Working Solution | Thermo Fisher Scientific | 2342797 |
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