Literature DB >> 24905337

Direct amplification of casework bloodstains using the Promega PowerPlex(®) 21 PCR amplification system.

Kerryn Gray1, Damian Crowle2, Pam Scott2.   

Abstract

A significant number of evidence items submitted to Forensic Science Service Tasmania (FSST) are blood swabs or bloodstained items. Samples from these items routinely undergo phenol:chloroform:isoamyl alcohol organic extraction and quantitative Polymerase Chain Reaction (qPCR) testing prior to PowerPlex(®) 21 amplification. This multi-step process has significant cost and timeframe implications in a fiscal climate of tightening government budgets, pressure towards improved operating efficiencies, and an increasing emphasis on rapid techniques better supporting intelligence-led policing. Direct amplification of blood and buccal cells on cloth and Whatman FTA™ card with PowerPlex(®) 21 has already been successfully implemented for reference samples, eliminating the requirement for sample pre-treatment. Scope for expanding this method to include less pristine casework blood swabs and samples from bloodstained items was explored in an endeavour to eliminate lengthy DNA extraction, purification and qPCR steps for a wider subset of samples. Blood was deposited onto a range of substrates including those historically found to inhibit STR amplification. Samples were collected with micro-punch, micro-swab, or both. The potential for further fiscal savings via reduced volume amplifications was assessed by amplifying all samples at full and reduced volume (25 and 13μL). Overall success rate data showed 80% of samples yielded a complete profile at reduced volume, compared to 78% at full volume. Particularly high success rates were observed for the blood on fabric/textile category with 100% of micro-punch samples yielding complete profiles at reduced volume and 85% at full volume. Following the success of this trial, direct amplification of suitable casework blood samples has been implemented at reduced volume. Significant benefits have been experienced, most noticeably where results from crucial items have been provided to police investigators prior to interview of suspects, and a coronial identification has been successfully completed in a short timeframe to avoid delay in the release of human remains to family members.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Casework bloodstains; Direct amplification; PowerPlex 21; STR

Mesh:

Year:  2014        PMID: 24905337     DOI: 10.1016/j.fsigen.2014.05.003

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  8 in total

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2.  [Polymorphism analysis of 20 autosomal short-tandem repeat loci in southern Chinese Han population].

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Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2016-02-20

3.  Direct-to-PCR tissue preservation for DNA profiling.

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Journal:  Int J Legal Med       Date:  2015-11-03       Impact factor: 2.686

4.  An evaluation of direct PCR amplification.

Authors:  Daniel E Hall; Reena Roy
Journal:  Croat Med J       Date:  2014-12       Impact factor: 1.351

5.  Characterization of degradation and heterozygote balance by simulation of the forensic DNA analysis process.

Authors:  Oskar Hansson; Thore Egeland; Peter Gill
Journal:  Int J Legal Med       Date:  2016-11-03       Impact factor: 2.686

6.  Inhibition mechanisms of hemoglobin, immunoglobulin G, and whole blood in digital and real-time PCR.

Authors:  Maja Sidstedt; Johannes Hedman; Erica L Romsos; Leticia Waitara; Lars Wadsö; Carolyn R Steffen; Peter M Vallone; Peter Rådström
Journal:  Anal Bioanal Chem       Date:  2018-03-05       Impact factor: 4.142

7.  Direct PCR amplification from saliva sample using non-direct multiplex STR kits for forensic DNA typing.

Authors:  Pankaj Shrivastava; Toshi Jain; R K Kumawat
Journal:  Sci Rep       Date:  2021-03-29       Impact factor: 4.379

8.  Comparison of customized spin-column and salt-precipitation finger-prick blood DNA extraction.

Authors:  Jun-Jie Poh; Samuel Ken-En Gan
Journal:  Biosci Rep       Date:  2014-10-22       Impact factor: 3.840

  8 in total

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