基于ITS2 条形码序列对新型“香料”毒品植物成分的研究
杨雪莹1, 曹海丹2, 裴黎1, 徐鹏1
1.公安部物证鉴定中心 法医遗传学公安部重点实验室,北京100038
2.长春理工大学,长春 130022

作者简介:杨雪莹(1980—),女,河北昌黎人,副主任法医师,博士,研究方向为法医遗传学。 E-mail:yxystyhhp@163.com

摘要

目的 应用DNA条形码片段ITS2对新型毒品样品中的植物成分进行分析。方法 提取可疑毒品样本“spike 99”,“K2”,“7号”中的植物基因组DNA,用ITS2通用引物进行扩增,对扩增产物进行测序,对序列校对拼接,应用BLAST方法在NCBI数据库中比对。结果 “spike 99”、“7号”各得到1条ITS2基因序列,“K2”得到2条ITS2基因序列,分别与紫花苜蓿、大麻、啤酒花、黄蜀葵的ITS2基因序列的同源性为100%。结论 应用条形码技术可以成功分析新型毒品中的植物种属,为案件中植物样本的种属鉴定提供方法。

关键词: 法医遗传学; ITS2基因; 毒品; 植物; 种属鉴定
中图分类号:DF795.2 文献标志码:B 文章编号:1008-3650(2015)01-0071-03 doi: 10.16467/j.1008-3650.2015.01.016
Identification of Plant Species in Spice Drugs Using ITS2 Barcode
YANG Xue-ying1, CAO Hai-dian2, PEI Li1, XU Peng1
1. Key Laboratory of Forensic Genetics, Institute of Forensic Science, Ministry of Public Security, Beijing 100038, China
2.Changchun University of Science and Technology, Changchun 130022, China
Abstract

Objective The genetic analysis of ITS2 region presented here is to detect the species of plants from spice drugs using DNA barcoding method.Methods DNA from samples of “spike 99”, “K2” and “7#” collected from cases were extracted using QIAGEN DNeasy plant mini kit. The ITS2 sequence forward primer was 5’-GCGATACTTGGTGTGAAT-3’, and the reverse was 5’-GACGCTTCTCCAGACTACAAT-3’. PCR amplification was performed in a 25µL reaction mixture. Purified PCR products were sequenced in both directions with the primers used for PCR amplification on 3730XL Genetic Analyzer. To estimate the quality of the generated sequence, the original forward and reverse sequences were assembled using CodonCode Aligner V 3.71 and the conserved 5.8S and 26S rRNA sequences were removed from the ITS2 sequence. The PCR amplification products using ITS2 primers were sequenced, analyzed and BLAST in NCBI database.Results The samples of “spike 99”, “K2” and “7#” contained organic compounds which had been determined by GC-MS. “spike 99” was found to possess JWH-073 and JWH-018 components, and JWH-018 in “K2”, cannabis in “7#”, respectively. As for the DNA analysis, one sequence from both “spike 99” and “7#” and two sequences from “K2” were 100% homologous with the ITS2 sequences of Medicago sativa, cannabis sativa, humulus lupulus and Abelmoschus manihot.Conclusions All samples containing constituents from at least four kinds of plants: Medicago sativa, cannabis sativa, humulus lupulus and Abelmoschus manihot. The results were consistent with their chemical constituents and gave the evidence that the DNA approach was an essential alternative to identify the species of plant for the drug abused. DNA barcoding, involving the amplification and sequencing of relatively short, standardized genetic loci, provides a powerful tool to identify the species of plant.

Keyword: forensic genetics; ITS2 gene; abused drugs; plant; species identification

近期在世界很多国家和地区出现一种新兴毒品, 形态与茶叶相似, 吸食方法与大麻(Cannabis sativa)相同, 燃烧会挥发出类似四氢大麻酚的物质(THC), 其主要成分是JWH-073(1-丁基-3-(1-萘甲酰基)吲哚)和JWH-018(1-戊基-3-(1-萘甲酰基)吲哚)的一种烷基同系物。这两种化合物均为合成大麻素, 能够与大麻素类似的受体结合, 产生的效力比天然大麻强4~10 倍, 能够迅速地从肺部转移到血液, 到达全身各器官, 吸食者可出现呕吐、妄想、精神恍惚和情绪失控等症状, 严重者会感到呼吸困难、心跳加速、激动和瞳孔放大等。这种毒品由多种植物混合制成, 吸毒者把它称作“ 香料” [1, 2, 3]。本研究使用DNA条形码鉴定技术, 采用ITS2 DNA 条形码片段, 对新型“ 香料” 毒品的植物成分进行鉴定研究, 为“ 香料” 毒品中有效成分的分析提供更确切的信息。

1 材料与方法
1.1 材 料

材料为某市查获的疑似毒品物质, 查获的部分样品外包装袋上标识为“ spike 99” , “ K2” , “ 7号” 。样品均为干燥植物成份, “ K2” 取两种不同颜色样本各1份(“ K2” -1, “ K2” -2)、“ spike 99” 、“ 7号” 各取1份, 每种样本各取30mg, 研磨成粉末, 利用QIAGEN DNeasy plant mini kit提取基因组DNA。

1.2 PCR 扩增及序列测定

采用正向引物5'-GCGATACTTGGTGTGAAT-3', 反向引物5'-GACGCTTCTCCAGACTACAAT-3'扩增ITS2片段。PCR 反应总体积为25μ L, 体系内含PCR mix 12.5μ L(Tiangen Biotech Co., 中国)、引物各1μ L(2.5μ mol/L), 总DNA 1μ L。PCR 反应程序为94℃, 预变性5min; 94℃ 30s, 56℃ 30s, 72℃ 45s, 40个循环; 72℃延伸10min。纯化PCR产物并使用ABI公司的3730XL 测序仪(美国Applied Biosystems公司)进行双向测序[4, 5]

1.3 序列分析

将测序得到的峰图应用CodonCode Aligner V3.71(美国CodonCode公司Dedham, MA)序列分析软件进行校正拼接, ITS2 序列用HMMer 注释法切除5.8S和26S 端, 保留ITS2 的全长, 应用BLAST方法在NCBI数据库中比对。

2 结果与分析

以植物样本基因组DNA 为模板, 扩增ITS2基因片段得到了清晰的PCR 产物, 空白对照无条带, 见图1

图 1 测试样品PCR产物电泳图。M:2000bp分子量标准品; 1-4 依次为“ spike 99” 、“ K2” -1、“ K2” -2、“ 7号” PCR产物。Fig. 1 Amplification of ITS2 from 4 samples. M: 2000bp molecular marker; Lane 1-4: “ spike 99” , “ K2” -1, “ K2” -2, “ 7#” .

将PCR 产物纯化后经3730XL测序仪进行测序, 将序列用HMMer注释法切除5.8和26S端, 保留ITS2的全长, 最终得到5条220~235bp 的序列。经BLAST比对, 同源性分析, 发现所检测的样本“ K2” -1 ITS2片段序列与啤酒花(Humuluslupulus)ITS2序列的同源性高达100%(见图2), “ K2” -2 ITS2片段序列与黄蜀葵(Abelmoschusmanihot)ITS2序列的同源性高达100%, “ 7号” ITS2片段序列与大麻(Cannabis sativa) ITS2序列的同源性高达100%, “ spike 99” ITS2片段序列与紫花苜蓿(Medicago sativa)ITS2序列的同源性高达100%。

图2 “ K2” -1 ITS2比对结果Fig. 2 Sequence alignment of “ k2” -1 with ITS2 sequences in NCBI database

3 讨 论

DNA 条形码技术是一种新兴的物种鉴定方法, 因其操作简单、通用性强、技术统一, 近年来逐渐成为物种鉴定研究的热门方法[6]。ITS2序列是位于核基因的一小段序列, 该序列在绿色植物中分布广泛, ITS2具有序列短、容易扩增、鉴定能力强等多个DNA条形码应有的优点, 是植物的DNA 条形码研究中最受关注的序列之一[4]

本研究基于ITS2条形码序列针对案件中缴获的“ spike 99” 、“ K2” 、“ 7号” 物质中的植物成分进行DNA提取, 通过PCR扩增, 获得了高纯度的ITS2基因片段, 在Gen-Bank通过BLAST 搜索、比对, 确定“ spike 99” 中植物成分与紫花苜蓿ITS2基因序列的部分片段的同源性高达100%; “ K2” 中检出两种植物成分分别与啤酒花、黄蜀葵的同源性为100%, “ 7号” 与大麻的同源性为100%。其中黄蜀葵与大麻外形相似, 为毒品原植物大麻的易混淆品种, 但它与紫花苜蓿、啤酒花均是有经济实用价值和药用价值的植物, 均不含有毒成分。针对本案例中缴获的“ spike 99” 、“ K2” 、“ 7号” 物质中的化学成分应用GC-MS 方法分析结果显示, “ K2” 的主要活性成分是JWH-018, “ spike 99” 主要的活性成分是JWH-073和JWH-018, “ 7号” 的主要活性成分是大麻[7, 8]。综上所述, 在本研究中, “ spike 99” 、“ K2” 中未检出天然大麻成分, 为非毒品原植物添加入人工合成大麻素成分制成的新型毒品, 这与化学成分分析结果一致。由于研究样本量有限, 而且形态不规则, 应用传统形态学很难确定其植物成分, DNA条形码技术因此成为植物形态学分类的有效补充, 可为物种鉴定提供更准确的信息, 相信随着该技术的日益成熟, 将会成为各类案件中的未知植物样本鉴定的有效手段。

The authors have declared that no competing interests exist.

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