Environmental factors and subsequent PCR inhibitors may affect the ability to retrieve DNA from handled objects. A poor quality DNA profile results from low DNA template or modifications imposed on the template (damage or degradation) prior to amplification. In this study, we show that direct PCR has the ability to amplify 'touch' DNA from uncleaned, handled, substrates following exposure to various environmental conditions. A variety of items (n=90), ranging from metal cartridge cases, glass, tape and wood were touched briefly (less than 15 seconds) by 4 volunteers, exposed to the environment overnight, and in one case for 8 days, and tested for the presence of surviving DNA. Informative DNA profiles were obtained from 49 out of the 90 items (a success rate of 54 %), with glass having the highest rate of DNA recovery. IntroductionSince its inception, research on 'touch' DNA samples has suffered from the problem that preserved endogenous DNA is often limited in quantity [1] and in various states of degradation [2]. It has been found that a significant number of crime-related surfaces, even though they should have DNA present, do not necessarily yield analytically useful material [3]. In natural conditions DNA is a hydrated macromolecule but outside its natural environment DNA becomes the target of several physical and chemical reactions [4]. There may be no surviving DNA left to capture on a handled object if the DNA is exposed to elements of heat, humidity, ultra violet (UV) light and bacterial growth, typical of an outdoor environment. Under these circumstances, standard protocols for swabbing and extracting 'touch' DNA from these items often recover sub-optimal levels of trace nuclear DNA [3] that can result in a poor quality STR-based DNA profile or no profile at all. The aim of this study is to determine the value of using the optimised swabbing technique [5] and direct PCR at amplifying 'touch' DNA from fingermarks as part of a mock case study.
Materials and methodsA number of precautions were taken for the handling and processing of 'touch' DNA samples; these have been extensively described elsewhere [5]. Four volunteers touched various substrates (wooden knife handles, glass, masking tape, brass cartridge cases, aluminium cartridge cases and nickel cartridge cases) for less than 15 seconds, before the items were left out-side in a shrub bed area. An indoor glass door was touched for less than 15 seconds to create fingerprint; these samples were not subjected to external conditions but were left for the same time period as other samples in the study. Substrates were not cleaned prior to touching to ensure results were as realistic as possible and to determine the extent of mixed DNA profiles. Environmental conditions were monitored. Sampling was repeated in triplicate for each volunteer. Twenty four hours later, or 8 days later (sample study 5), items were collected/processed (n = 90) and for wood, glass and cartridge cases a targeted swabbing approach was used [5] subsequent to direct PCR. For masking tap...