Forensic Science International: Genetics
Volume 4, Issue 4 , Pages 228-231, July 2010

Shotgun metagenomics of biological stains using ultra-deep DNA sequencing

  • B. Brenig

      Affiliations

    • Institute of Veterinary Medicine, University of Göttingen, Burckhardtweg 2, 37077 Göttingen, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49 551 393383; fax: +49 551 393392.
  • ,
  • J. Beck

      Affiliations

    • Institute of Veterinary Medicine, University of Göttingen, Burckhardtweg 2, 37077 Göttingen, Germany
    • Chronix Biomedical GmbH, Goetheallee 8, 37073 Göttingen, Germany
  • ,
  • E. Schütz

      Affiliations

    • Institute of Veterinary Medicine, University of Göttingen, Burckhardtweg 2, 37077 Göttingen, Germany
    • Chronix Biomedical GmbH, Goetheallee 8, 37073 Göttingen, Germany

Received 28 November 2008; received in revised form 30 September 2009; accepted 2 October 2009. published online 02 November 2009.

Abstract 

A detailed molecular analysis of blood or other biological stains at a crime scene is often hampered by the low quantity and quality of the extractable DNA. However, the determination of the origin and composition of a stain is in most cases a prerequisite for the final elucidation of a criminal case. Standard methodologies, e.g. amplification of DNA followed by microsatellite typing or mitochondrial DNA sequencing, are often not sensitive enough to result in sufficient and conclusive data. We have applied ultra-deep DNA sequencing using the 454 pyrosequencing technology on a whole genome amplified (WGA) environmental biological stain, which was analysed unsuccessfully with standard methodologies following WGA. With the combination of WGA and 454 pyrosequencing, however, we were able to generate 7242 single sequences with an average length of 195bp. A total of 1,441,971bp DNA sequences were generated and compared with public DNA sequence databases. Using RepeatMasker and basic logical alignment search tool (BLAST) searches against known microbial and mammalian genomes it was possible to determine the metagenomic composition of the stain, i.e. 4.2% bacterial DNA, 0.3% viral DNA, 2.7% fungal DNA, 10.3% mammalian repetitive DNA, 0.9% porcine DNA, 0.13% human DNA and 81.5% DNA of unknown origin. Our data demonstrate that 454 pyrosequencing has the potential to become a powerful tool not only in basic research but also in the metagenomic analysis of biological trace materials for forensic genetics.

Keywords: Forensic science, Biological stain, Ultra-deep DNA sequencing, 454 pyrosequencing, Species identification

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PII: S1872-4973(09)00150-1

doi:10.1016/j.fsigen.2009.10.001

Forensic Science International: Genetics
Volume 4, Issue 4 , Pages 228-231, July 2010