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The aim of this study was to analyse the susceptibility of Enterobacteriaceae strains isolated from food to antibiotics used in human therapy. The tests were conducted on 433 samples of raw and processed meat intended for sale. A total of 114 strains belonging to Enterobacteriaceae were isolated by the classical bacteriological technique. Escherichia, Klebsiella, Serratia, Enterobacter, Proteus, Hafnia, Citrobacter, Salmonella and Shigella were cultured from samples of beef, pork, poultry and ready-made meat products. Antibiotic susceptibility was tested by the mean of E-tests for the following antibiotics: piperacillin, piperacillin with tazobactam, cefotaxime, cefuroxime, imipenem, ceftazidime, gentamycin, tobramycin, ciprofloxacin and trimethoprim with sulfamethoxazole. Over 37% of the strains isolated were resistant to some of these antibiotics, and 34% showed resistance to at least 2 of them. Resistance was observed most frequently to cephalosporins, penicillins and trimethoprim with sulfamethoxazole, which may suggest that these antibiotics are used excessively in veterinary medicine.
 One of the mechanisms of Candida albicans resistance to azole drugs used in antifungal therapy relies on increased expression and presence of point mutations in the ERG11 gene that encodes sterol 14α demethylase (14DM), an enzyme which is the primary target for the azole class of antifungals. The aim of the study was to analyze nucleotide substitutions in the Candida albicans ERG11 gene of azole-susceptible and azole-resistant clinical isolates. The Candida albicans isolates represented a collection of 122 strains selected from 658 strains isolated from different biological materials. Samples were obtained from hospitalized patients. Fluconazole susceptibility was tested in vitro using a microdilution assay. Candida albicans strains used in this study consisted of two groups: 61 of the isolates were susceptible to azoles and the 61 were resistant to azoles. Four overlapping regions of the ERG11 gene of the isolates of Candida albicans strains were amplified and sequenced. The MSSCP (multitemperature single strand conformation polymorphism) method was performed to select Candida albicans samples presenting genetic differences in the ERG11 gene fragments for subsequent sequence analysis. Based on the sequencing results we managed to detect 19 substitutions of nucleotides in the ERG11 gene fragments. Sequencing revealed 4 different alterations: T495A, A530C, G622A and A945C leading to changes in the corresponding amino acid sequence: D116E, K128T, V159I and E266D. The single nucleotide changes in the ERG11 gene did not affect the sensitivity of Candida albicans strains, whereas multiple nucleotide substitutions in the ERG11 gene fragments indicated a possible relation with the increase in resistance to azole drugs.
The frequency of Pneumocystis carinii occurrence in BAL of 38 HIV-infected patients was determined with three different method. BAL sediments were stained with Giemsa method, silvered according to Gomori-Grocott method and studied with indirect immunofluorescence assay. Using Giemsa method staining Pneumocystis carinii was diagnosed in 81,6% of patients, in Gomori-Grocott method - in 31,6% of patients, but results of indirect immunofluorescence assay were positive only in 23,7%. In our study staining BAL sediments with Giemsa method allowed to detect Pneumocystis carinii in the highest percentage of examined patients.
The aim of this study was the evaluation of the influence of extremely low-frequency magnetic fields (ELF-MF) on the morphology of thyroid epithelial cells in female rats. The rats were exposed to ELF–MF (frequency: 5-10 Hz, induction 10 mT), 1 hour daily for 7 days over a week for 4 months. Control animals were sham exposed. After that time the rats were sacrificed by anaesthetizing with Ketamine and decapitated. The animals’ thyroid glands were extracted. They served as microscopic preparations. In the preparations, the thyreocytes, nuclei, nucleoli and nucleo-cytoplasmatic ratio were evaluated. We concluded that changes in the location of nuclei, surface field, the number and surface of nucleoli and nucloli organizers show an increase in reply activity in the nuclei of thyreocytes and a probable increase of DNA synthesis.
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