Bacterial Deposition of Gold on Hair: Archeological, Forensic and Toxicological Implications

Trace metal analyses in hair are used in archeological, forensic and toxicological investigations as proxies for metabolic processes. We show metallophilic bacteria mediating the deposition of gold (Au), used as tracer for microbial activity in hair post mortem after burial, affecting results of such analyses. Methodology/Principal Findings Human hair was incubated for up to six months in auriferous soils, in natural soil columns (Experiment 1), soils amended with mobile Au(III)-complexes (Experiment 2) and the Au-precipitating bacterium Cupriavidus metallidurans (Experiment 3), in peptone-meat-extract (PME) medium in a culture of C. metallidurans amended with Au(III)-complexes (Experiment 4), and in non-auriferous soil (Experiment 5). Hair samples were analyzed using scanning electron microscopy, confocal microscopy and inductively coupled plasma-mass spectrometry. In Experiments 1–4 the Au content increased with time (P = 0.038). The largest increase was observed in Experiment 4 vs. Experiment 1 (mean = 1188 vs. 161 µg Kg−1, Fisher's least significance 0.001). The sulfur content, a proxy for hair metabolism, remained unchanged. Notably, the ratios of Au-to-S increased with time (linear trend P = 0.02) and with added Au and bacteria (linear trend, P = 0.005), demonstrating that larger populations of Au-precipitating bacteria and increased availability of Au increased the deposition of Au on the hair. Conclusion/Significance Interactions of soil biota with hair post mortem may distort results of hair analyses, implying that metal content, microbial activities and the duration of burial must be considered in the interpretation of results of archeological, forensic and toxicological hair analyses, which have hitherto been proxies for pre-mortem metabolic processesGenevieve Phillips, Frank Reith, Clifford Qualls, Abdul-Mehdi Ali, Mike Spilde and Otto Appenzelle

Molecularly imprinted polypyrrole sensors for the detection of pyrene in aqueous solutions

Recently, electrochemical sensors have emerged as tools for polyaromatic hydrocarbons (PAH) detection that are cost-effective, easy to produce and use, highly selective and sensitive, and with good reproducibility. Polypyrrole may be easily produced from polymerization of pyrrole, by chemical as well as electrochemical methods, to produce dimensionally stable semi-conductive polymer materials, under mild synthesis conditions. In this study, polypyrrole was used as the stable molecular framework within which to create an imprint of the desired polyaromatic hydrocarbon, in situ, at glassy carbon electrodes. The molecularly imprinted polymer (MIP) sensors were washed to remove the imprint and subsequently characterized by atomic force microscopy (AFM), scanning electron microscopy (SEM), and cyclic voltammetry (CV). The MIP sensors were then applied to the detection of pyrene and non-imprinted polymers (NIP) sensors were also evaluated for comparison with the MIP sensors. Calibration curves obtained for the detection of the pyrene at the MIP sensors in aqueous media reported limits of detection (LOD) of 2.28 × 10−7 M for pyrene and limit of quantification (LOQ) of 6.92 × 10−7 M (n = 3). The sensitivity of the MIP sensors (32.53 A/M) determined from the slopes of the calibration curves reported twice the value measured for NIP sensors (14.48 A/M)