ABSTRACT
Set-shifting and maintenance are complex cognitive processes, which are often impaired in schizophrenia. The genetic basis of these processes is poorly understood. We aimed to investigate the association between genetic variants of the metabotropic glutamate receptor 3 (GRM3) and cognitive set-shifting in healthy individuals. The relationship between 14 selected single nucleotide polymorphisms (SNPs) of the GRM3 gene and cognitive set-shifting as measured by perseverative errors using the modified card sorting test (MCST) was analysed in a sample of N = 98 young healthy individuals (mean age in years: 22.7 +/- 0.19). Results show that SNP rs17676277 is related to the performance on the MCST. Subjects with the TT genotype showed significantly less perseverative errors as compared with the AA (P = 0.025) and AT (P = 0.0005) and combined AA/AT genotypes (P = 0.0005). Haplotype analyses suggest the involvement of various SNPs of the GRM3 gene in perseverative error processing in a dominant model of inheritance. The findings strongly suggest that the genetic variation (rs17676277 and three haplotypes) in the metabotropic GRM3 is related to cognitive set-shifting in healthy individuals independent of working memory. However, because of a relatively small sample size for a genetic association study, the present results are tentative and require replication.
Subject(s)
Decision Making/physiology , Problem Solving/physiology , Receptors, Metabotropic Glutamate/genetics , Set, Psychology , Adult , Analysis of Variance , Cognition/physiology , Cross-Sectional Studies , Female , Genetic Variation , Haplotypes , Humans , Linkage Disequilibrium , Male , Polymorphism, Single Nucleotide/genetics , Receptors, Metabotropic Glutamate/physiology , Reference Values , Young AdultABSTRACT
An improved nucleic acid amplification test (NAAT) to detect Chlamydia trachomatis infections, based on PCR amplification within its cryptic plasmid (CT1/CT2 Test) was developed. DNA was extracted from urogenital swabs and a 594-bp long DNA fragment from the cryptic plasmid (pCT) was amplified. The sensitivity and specificity of the CT1/CT2 Test were determined to be 100 and 99%, respectively, when directly compared with current amplification kit for sexually transmitted diseases (MPCR). Basic epidemiological data related to the patients attending gynecological and/or urological clinics are also provided. The overall prevalence rate in this group of patients suspected for C. trachomatis infection was determined to be about 95 per 1000 (88 and 107 per 1000 in females and males, respectively). It demonstrates that the CT1/CT2 Test is suitable for epidemiological screening and/or diagnostic practice.
Subject(s)
Chlamydia Infections/diagnosis , Chlamydia trachomatis/isolation & purification , Female Urogenital Diseases/microbiology , Male Urogenital Diseases/microbiology , Polymerase Chain Reaction/methods , Adolescent , Adult , Aged , Chlamydia Infections/epidemiology , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Female , Female Urogenital Diseases/diagnosis , Female Urogenital Diseases/epidemiology , Humans , Male , Male Urogenital Diseases/diagnosis , Male Urogenital Diseases/epidemiology , Middle Aged , Plasmids/chemistry , Plasmids/genetics , Sensitivity and Specificity , Sequence Analysis, DNA , Slovakia/epidemiologyABSTRACT
A simple nucleic acid amplification test (NAAT) was developed for detection of Ureaplasma urealyticum infection based on the PCR amplification of the urease gene (UU1/UU2 Test). DNA was extracted from urogenital swabs and a 225-bp long DNA fragment was amplified by PCR. NAAT was compared to the commercial amplification kit for sexually transmitted disease reference assay. The sensitivity and specificity of the UU1/UU2 Test were determined to be 100 and 98.9%, respectively. The overall prevalence rate in this group of patients was found to be about 236 per 1000 (283 and 166 per 1000 in females and males, respectively). These data demonstrate that UU1/UU2 Test is suitable for effective epidemiological screening and/or diagnostic practice.
Subject(s)
Female Urogenital Diseases/microbiology , Male Urogenital Diseases/microbiology , Polymerase Chain Reaction/methods , Ureaplasma Infections/diagnosis , Ureaplasma urealyticum/isolation & purification , Adolescent , Adult , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Female , Female Urogenital Diseases/diagnosis , Female Urogenital Diseases/epidemiology , Humans , Male , Male Urogenital Diseases/diagnosis , Male Urogenital Diseases/epidemiology , Middle Aged , Sensitivity and Specificity , Sequence Analysis, Protein , Slovakia/epidemiology , Ureaplasma Infections/epidemiology , Ureaplasma Infections/microbiology , Ureaplasma urealyticum/genetics , Urease/chemistry , Urease/geneticsABSTRACT
Sera of 426 adult persons were examined to assess the prevalence of SEN virus (SENV) infection in Slovakia and to determine the importance of different risk factors for parenteral transmission. SENV prevalence was determined by the PCR method using primers of SENV-D and SENV-H strains. Positive results were found in 10 of 37 patients with acute hepatitis of unknown etiology, 7 of 38 with acute hepatitis B, 17 of 44 with chronic hepatitis B, 29 of 102 with chronic hepatitis C, 36 of 72 hemodialysis patients, 2 of 33 health care workers and 24 of 100 persons from the control group. The highest prevalence of SENV was among hemodialysis patients, significantly higher than in the groups of health care workers, acute hepatitis B and controls. The lowest prevalence was in health care workers group, significantly lower also in comparison with groups of chronic hepatitis B and C. Among the possible risk factors of virus transmission the average duration of hemodialysis (1.15 vs. 0.50 years), number of surgeries (1.60 vs. 1.10) and transfusions (1.34 vs. 0.94) showed notable differences in terms of SENV infection. Bilirubin and aminotransferase levels did not differ between SENV-positive and -negative groups. No pathogenetic role of SEN virus in liver injury was confirmed.
Subject(s)
DNA Virus Infections/epidemiology , Liver Diseases/virology , Torque teno virus , Adult , Aged , DNA, Viral/analysis , Female , Humans , Liver Diseases/epidemiology , Male , Middle Aged , Polymerase Chain Reaction , Renal Dialysis/adverse effects , Risk Factors , Slovakia/epidemiology , Statistics, Nonparametric , Surgical Procedures, Operative/adverse effects , Torque teno virus/genetics , Transfusion ReactionABSTRACT
Verotoxin-producing Escherichia coli (VTEC) are nowadays among the most important emerging group of food-borne pathogens (VTEC strains cause gastroenteritis that can be complicated by the hemorrhagic colitis or hemolytic uremic syndrome, HUS). Escherichia coli 026 producing verotoxin 2 was isolated and its identity confirmed by examination of phenotype and genotype; the strain was first described in Slovakia in association with the development of HUS in a 4-year-old girl.
Subject(s)
Escherichia coli/isolation & purification , Hemolytic-Uremic Syndrome/diagnosis , Hemolytic-Uremic Syndrome/microbiology , Shiga Toxins/biosynthesis , Child, Preschool , Escherichia coli/classification , Escherichia coli/genetics , Escherichia coli Infections/diagnosis , Escherichia coli Infections/microbiology , Feces/microbiology , Female , Humans , SerotypingABSTRACT
In total, 201 alpha-haemolytic Escherichia coli isolates from various clinical materials (urine samples and vaginal and rectal swabs) were examined by PCR for the presence of genes for the virulence factors alpha-haemolysin (hly), cytotoxic necrotising factor type 1 (cnf1), P-fimbriae (pap), S/F1C-fimbriae (sfa/foc), aerobactin (aer) and afimbrial adhesin (afaI). Among vaginal isolates, 96% were positive for cnf1, compared with 80% of urine strains (p 0.02) and 63% of rectal strains (p 0.0001). Similarly, sfa/foc-specific DNA sequences were found in 97% of vaginal isolates compared with 75% of rectal strains (p 0.004). The afa1 and aer genes were associated more with rectal alpha-haemolytic E. coli strains than with extra-intestinal isolates. The results suggested that CNF1 and/or S/F1C-fimbriae contribute to colonisation and persistence of alpha-haemolytic E. coli strains in the vaginal environment.
