Tracking plant, fungal, and bacterial DNA in honey specimens

J Forensic Sci. 2012 Jan;57(1):222-7. doi: 10.1111/j.1556-4029.2011.01964.x. Epub 2011 Nov 10.

Abstract

Consuming honey can result in adverse effects owing to poisoning by bacterial (botulism) or plant toxins. We have devised a method to extract polymerase chain reaction (PCR) amplifiable DNA of up to c. 400 bp in length based on dialysis of a 15-mL honey sample for 18 h against deionized water followed by sequential extraction using phenol, phenol/chloroform/isoamyl alcohol, chloroform/isoamyl alcohol, and ether. Sequence analysis of PCR products obtained using "universal" plant, fungal, and bacterial primers targeted to the ribosomal RNA genes has allowed us to identify six different orders of plants (Apiales, Fabales, Asterales, Solanales, Brassicales, and Sapindales), two orders of fungi (Entylomatales and Saccharomycetales), and six orders of bacteria (Sphingomonadales, Burkholderiales, Pseudomonadales, Enterobacteriales, Actinomycetales, and Bifidobacteriales) in a single honey specimen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Primers
  • DNA, Bacterial / isolation & purification*
  • DNA, Fungal / isolation & purification*
  • DNA, Plant / isolation & purification*
  • Electrophoresis, Agar Gel
  • Gram-Negative Bacteria / genetics
  • Gram-Positive Bacteria / genetics
  • Honey / adverse effects*
  • Honey / microbiology*
  • Magnoliopsida / genetics
  • Polymerase Chain Reaction

Substances

  • DNA Primers
  • DNA, Bacterial
  • DNA, Fungal
  • DNA, Plant