Species identification of cannabis sativa using real-time quantitative PCR (qPCR)

Christopher E. Johnson, Amritha Premasuthan, Jessica Satkoski Trask, Sree Kanthaswamy

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

Most narcotics-related cases in the United States involve Cannabis sativa. Material is typically identified based on the cystolithic hairs on the leaves and with chemical tests to identify of the presence of cannabinoids. Suspect seeds are germinated into a viable plant so that morphological and chemical tests can be conducted. Seed germination, however, causes undue analytical delays. DNA analyses that involve the chloroplast and nuclear genomes have been developed for identification of C. sativa materials, but they require several nanograms of template DNA. Using the trnL 3′ exon-trnF intragenic spacer regions within the C. sativa chloroplast, we have developed a real-time quantitative PCR assay that is capable of identifying picogram amounts of chloroplast DNA for species determination of suspected C. sativa material. This assay provides forensic science laboratories with a quick and reliable method to identify an unknown sample as C. sativa.

Original languageEnglish (US)
Pages (from-to)486-490
Number of pages5
JournalJournal of Forensic Sciences
Volume58
Issue number2
DOIs
StatePublished - Mar 1 2013
Externally publishedYes

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Keywords

  • Cannabis
  • CpDNA
  • Forensic science
  • Marijuana
  • Species determination
  • TaqMan™ assay
  • qPCR

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Genetics

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