Abstract

Cannabis sativa is the most used controlled substance in Europe. With the advent of new and less restrictive European laws on cannabis sale for recreational use (including in Italy), an increase in indoor cannabis crops were observed. This increase was possible due to the availability of cannabis seeds through the internet market. Genetic identification of cannabis can link seizures and if in possession then might aid in an investigation. A 13-locus multiplex STR method was previously developed and validated by Houston et al. A collaborative exercise was organized by the Italian Forensic Geneticists – International Society of Forensic Genetics (Ge.F.I. – ISFG) Working Group with the aim to test the reproducibility, reliability and robustness of this multiplex cannabis STR kit. Twenty-one laboratories from three European countries participated in the collaborative exercise and were asked to perform STR typing of two cannabis samples. Cannabis DNA samples and the multiplex STR kit were provided by the University of Barcelona and Sam Houston State University. Different platforms for PCR amplification, capillary electrophoresis (CE) and genotyping software were selected at the discretion of the participating laboratories. Although the participating laboratories used different PCR equipment, CE platforms and genotyping software, concordant results were obtained from the majority of the samples. The overall genotyping success ratio was 96%. Only minor artifacts were observed. The mean peak height ratio was estimated to be 76.3% and 78.1% for sample 1 and sample 2, respectively. The lowest amount of −1 / + 1 stutter percentage produced, when the height of the parent allele was higher than 8000 RFU, resulted to be less than 10% of the parent allele height. Few common issues were observed such as a minor peak imbalance in some heterozygous loci, some artifact peaks and few instances of allelic drop-out. The results of this collaborative exercise demonstrated the robustness and applicability of the 13-locus system for cannabis DNA profiling for forensic purposes.

Highlights

  • C. sativa is the subject of one of the most common drug law of­ fenses in Europe

  • Genotyping errors may be due to partial DNA degradation, amplification errors, stutter calculation errors, bin error and PCR artifacts such as standard deviation (SD): Standard Deviation; Minimum peak height ratio (PHR): Minimum PHR observed value for that locus; Maximum PHR: Maximum PHR observed value for that locus; Median PHR: Min PHR/Max PHR; Mean Peak Height across all heterozygous loci: Medium value for Heterozygous loci was 74.15% for the positive control, Inter Loci Balance: Mean PHR/Maximum Peak Height (MPH)

  • The −1/+ 1 stutter percentage raised when the parent peak height was lower than 800 relative fluorescence units (RFU) and it decreased when the parent peak height was higher than 1500 RFU

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Summary

Introduction

C. sativa is the subject of one of the most common drug law of­ fenses in Europe. Since 2014, cannabis accounted for almost 60% of an overall estimate of 1.6 million offenses including possession and trafficking [1]. Cannabis can be classified into legal fiber type (hemp) and illegal drug type (marijuana). Marijuana differs from hemp based on the high level of Δ9-tetrahydrocannabinol (Δ9-THC). In Italy, the possession of limited amounts of marijuana, i.e., containing 500 mg of Δ9-THC [2], is considered only a civil offense. On the contrary, trafficking and selling cannabis is prohibited and punished by law. Support and promotion of hemp crops is allowed for textiles, food, cosmetic production and bioengineering industry [3]

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