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Yeast like fungi of Malassezia pachydermatis species are numbered among the opportunistic agents accounting for acute dermatoses or even systemic infections in people and animals. They exhibit the clear heterogeneity pertaining to the phenotypic traits and growth requirements. The objective of the present study was to determine the degree of variation as well as the biochemical profiles of M. pachydermatis strains. The studies were conducted on 40 strains isolated from the auditory canal of healthy dogs and those with otitis externa symptoms recognized. An assessment was conducted of the traits of fungus morphology (size and shape of cells and colony type), expression of extracellular hydrolases (API-ZYM) and the activity of catalase, urease, caseinase, beta-glucosidase, phospholipase and Tween hydrolases: 20, 40, 60 and 80. The obtained results made it possible to determine the general metabolism pattern for this species: no fermentability or capacity for assimilation of most carbohydrates, poor proteolytic properties, high activity of enzymes from the phosphatase and lipolytic enzymes groups. On the grounds of the statistical analysis, the examined strains were classified into 7 separate groups of congenial morphology and a determined level of enzymatic activity. Biotype I includes large, smooth and creamy-white colonies of high metabolic activity; moreover, they exhibit high sensitivity to the inhibitory operation of Tween 20 and Cremophor EL; biotype II exhibits a rough type of colony growth, the lowest metabolic activity and a lack of expression of lipase C14 and enzymes from the arylamidase group; biotype III comprises the strains of large, smooth colonies, poor total enzymatic activity and with no activity of cystynic arylamidase; biotype IV includes the strains of small and smooth colonies, average metabolic activity but with optimal usability of Tween 40 and 60 hydrolysis products for growth; biotype V groups the strains of the average metabolic activity and without phospholipase activity recorded; biotype VI comprises the strains of smooth, large or medium-sized colonies and a relatively high enzymatic activity as well as the highest level for alkaline phosphatase and valine arylimidase, phospholipase, catalase, caseine, Tween 80 hydrolase; biotype VII is characterized by the highest total enzymatic activity, high capacity for eskulin break-down, Tween 40, 60 and 80 hydrolysis. Further studies are needed to demonstrate a correlation between the strain classification into a defined biotype and its ecologic or clinical status.
The aim of the study was to make an attempt at showing the intraspecies heterogenecity of Malassezia pachydermatis strains with regards to their origin (strains isolated from healthy dogs and with otitis externa symptoms). The study included 41 strains of Malassezia pachydermatis species isolated in a pure culture from dogs with clinical otitis externa symptoms (n = 20), clinically healthy dogs (n = 20) and a reference strain, M. pachydermatis (CBS7925). In order to isolate the genetic material from the fungal cells, the following four procedures were selected: mechanical, enzymatic, thermal and chemical. Considering the yield and repeatability of a method for the genomic DNA extraction, a mechanical method was applied. The genetic material research of each strain was performed according to PCR-REA technique with the amplification of three genome regions: ITS, LSU rRNA and a gene encoding beta-tubuline. The ITS and LSU rRNA regions were amplified employing the standard PCR reagents, whereas the region coding beta-tubuline with the so called touch down. The obtained amplification products were subjected to restrictive analysis by means of the following enzymes: EcoRI, Ncol, Hinfl, Alul, and Eco881 (Aval). The performed investigations made it possible to reveal the genotypic differentiation within M.pachydermatis species as well as some correlation between a genotypic profile and the origin of a strain (from healthy animals or with otitis externa symptoms), which may imply the existence of genetic conditioning of the Malassezia strains’ pathogenicity.
We have evalueated the activity of acidous asparagine protease in 48 strains of Candida isolated from homogenates of palatine tonsils from 116 patients after tonsilectomy. Strains most frequently isolated were C. albicans (66.7±6.8 %) and C. tropicalis (14.6±5.09 %). The range of proteolysis zone for Candida strains was 4.6 to 12.5 mm. Over 60% of the studied strains showed high and very high proteolytic activity (>6.6 mm) and the remaining strains with showed moderate activity (4.6-6.5). There were no strains with low medium activity (to 4.5 mm zone). The range of the number of rosettes E formed by lymphocytes obtained from the studied tonsils was 0-268.3. Lymphocytes isolated from 70 % of tonsils infected with Candida formed only 0-130 rosettes E; in the remaining cases the number ranged between 131 and 220. The number of lymphocytes T forming rosettes E isolated from palatine tonsils from patients not infected with fungi was 2.5 times higher. There was no correlation between the size of proteolysis zone and the number of rosettes E.
We have investigated the hydrolytic activity of 21 species of yeast-like fungi from Candida genus and l species of yeast S. cerevisiae isolated from Sulejów Reservoir water. The activity of hydrolytic enzymes of the studied fungi was different than that of standard strains and also of fungi isolated from patients. This difference demonstrates the capability of the studied fungi to adapt to various environmental conditions.
The study included 52 children. During endoscopy the contents of oesophagus, stomach and duodenum were collected with catheters, and additionally washings from the oral cavity and anal swabs or samples of faeces. Materials were inoculated on Sabouraud's media. The axenic strains of fungi were identified using own methods and others tests (API 20C, API 20C AUX). The activity of ketoconazole (K) was measured against 100 strains of Candida: C. albicans (91 strains), C. kefyr (4), C. famata (2). C. tropicalis (1), C. guilliermondii (1), C. glabrata (1). The strains susceptibility to K (RO4 1400 Janssen) was estimated with the own system based on the dose - response curves; the minimal inhibitory concentration (MIC) values were canculated. The low values of MIC indicate high susceptibility to K of examined Candida strains.
Hydrofobowe właściwości powierzchni komórkowej uznawane są za czynnik wirulencji drobnoustrojów. Są niespecyficznym czynnikiem adhezji patogenów do komórek gospodarza i powierzchni biomateriałów oraz warunkują oporność mikroorganizmów na fagocytozą. W niniejszej pracy dokonano oceny powierzchniowych właściwości gatunków Candida sp. w zależności od warunków wzrostu.
The aim of the work was to assess the enzymatic activity of 11 fungi strains isolated from the skin of 10 Łódź residents who had visited the tropics over 1998-1999. The strains were cultured by Jeske and Lupa of The Voivodeship Outpatient Clinie of Infectious, Parasitic and Tropical Diseases and Fungal Infections in Łódź. They were as follows: Trichophyton rubrum and Acremonium kiliense from Zambia, Myriodontium keratinophilum, Beauveria bassiana, Cladosporium herbarum, Candida famata and Trichophyton yaoundei from Sudan, Trichophyton tonsurans from Ethiopia, Trichophyton phaseliforme from Egypt, Acremonium strictum from Zimbabwe and Microsporum racemosus from Tanzania. The enzymatic activity was determined with the use of API ZYM of bioMerieux enabling 19 hydrolases to be revealed. In general, all tropical strains were characterised by a weak hydrolytic activity.
Characteristics or phenotypic specific and intraspecific reatures of fungal strains isolated from the organ ontocenoses in patients after renal transplantation. The aim of present study was to describe 60 specific and intraspecific features of fungal strains isolated from the organ ontocenoses: oral cavity, rectum and genital organs in 32 patients undergoing permanent immunosupression after renal transplantation. Fungal strains identified using API 20 C and API 20 C AUX (bioMérieux). The activity or 19 hydrolases was investigated using API ZYM. Among 41 strains of fungi the following were found: Candida albicans (31 strains), C. glabrata (5), C. guilliermondii (2), C. krusei (2) and Saccharomyces cerevisiae (1). The number of fungal strains isolated from the oral cavity was the highest (21), less numerous from rectum (12) and the least from the genital organs (8). The enzymograms were described for all strains and the highest activity was noted in case of: e₆ -leucine arylamidase, e₁₁-phosphatase acid, e₃-esterase (C4), e₁₂-naphtol-AS-BI-phosphohydrolase. The activity of these enzymes is connected with higher pathogenicity of C. albicans strains.
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