RESUMO
The purpose of the work is to determine the capabilities of the modern multifunctional device «Photobox 3138¼ with LED illuminators with a high color rendering index for photofixation, colorimetric, spectrozonal and multispectral analyzes of forensic objects. The competencies of the «Photobox 3138¼ device were experimentally revealed in terms of visualization and photofixation of both traces of biological origin (blood, sweat fat, saliva, etc.) and traces of traditional examinations, including shot products, oil products. The design of the device with a working field of 300×300 mm provides for the optimal arrangement of LED illuminators, including white light with a high color rendering index; spectrum-zonal illuminator with 4 types of LEDs with narrow non-intersecting spectral lines (458.1; 523.1; 594.1 and 630.6 nm) in the visible range of the spectrum; UV- (370 nm) and IR- (850 nm) illuminators. The fundamental possibility of using the resulting digital images of forensic objects for subsequent mathematical processing is experimentally shown. Images taken in different spectral ranges help to detect traces and damage. It was found that «Photobox 3138¼ allows you to solve a variety of diagnostic tasks related to the search, visualization, fixation and analysis of trace information.
Assuntos
Medicina LegalRESUMO
The distribution of the allele and genotype frequencies of polymorphic loci of serotonin receptor genes (HTR1A, rs6295; HTR2A, rs6311; HTR1B, rs6296) in Hadza (n = 197) and Datoga males (n = 230) living in Tanzania was determined. It was shown that the populations significantly differ by the frequencies of alleles and genotypes of the rs6295 locus of the HTR1A gene. The G-allele (0.779) and the genotype G/G (0.590), which are markers of increased risk of suicidal and impulsive behavior, respectively, are revealed in Hadza with high frequency. It was found that the frequency of homozygous G/G of the rs6296 locus of the HTR1B gene, which is a marker of increased risk of outward directed aggression, is higher in Datoga (0.563) than in Hadza (0.457). The allele and genotype frequencies of the rs6311 locus of the HTR2A gene do not differ among the Hadza and Datoga males. The data on the distribution of allele and genotype frequencies of the HTR1A, HTR2A, and HTR1B genes can be used to determine the associations of the identified markers with various forms of human aggressive behavior.
Assuntos
Agressão , Loci Gênicos , Polimorfismo Genético , Receptor 5-HT1A de Serotonina/genética , Receptor 5-HT1B de Serotonina/genética , Humanos , Masculino , Tanzânia/etnologiaRESUMO
The most frequent causative agents of cercarial dermatitis in Europe are the avian schistosomes of the genus Trichobilharzia . They preferably parasitize birds of the Anatidae. Trichobilharzia spp. schistosomes are also able to penetrate mammalian skin, posing a health risk to mammals, including humans. Currently several loci from nuclear and mitochondrial genomes are determined for European species of Trichobilharzia . Among them there is 1 genome sequence, ToSau3A, which is suitable for detection of Trichobilharzia spp. infection in aquatic systems. In the present paper, we used a PCR assay to obtain novel genome sequences from cercariae isolates of 3 European bird schistosome species ( Trichobilharzia franki , Trichobilharzia szidati , and Trichobilharzia regenti ) collected from freshwater ponds in Belorussia and Russia. We applied RAPD-fingerprinting using 1 random primer to differentiate 3 trichobilharzian species and subsequently cloned and sequenced putative species-specific RAPD fragments. One of them (410 bp in length), which was obtained for T. franki , revealed 64% homology with the repeat region of Schistosoma mansoni (GenBank FN357352) and turned out to be suitable for designing a specific primer pair (TR98F and TR98R) to detect 7 novel DNA sequences in the genome of 3 European Trichobilharzia species. The newly designed primer pair was found to be potentially suitable for PCR-based detection of trichobilharzian infection in snails. PCR primers TR98F and TR98R amplified only the DNA isolated from cercariae and sporocysts of 3 trichobilharzian species, but neither the DNA of 3 other digenean species ( Bilharziella polonica , Apatemon sp., and Diplostomum sp.) nor the DNA of uninfected host snails ( Lymnaea stagnalis , Radix auricularia , and Radix ovata ).
