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Candida albicans is a major human fungal pathogen especially as an etiologic agent of opportunistic oral and genital infections. Moreover, C. albicans can be involved in the deep infections and recent evidence suggests that the majority of diseases produced by this pathogen are associated with biofilm growth. The aims of this study were to evaluate biofilm production ability of C. albicans strains isolated from different sources, and to evaluate the effect of serum for enhancement the growth of biofilm. The strains used in this study were obtained from three sources; 12 from feces of patients with gastrointestinal disturbances, 13 from the oral cavity of patients with oral candidiasis, and 16 from the vagina of patients with Candida vulvovaginitis (CVV). Polystyrene 96-well plates were used to grow biofilms and crystal violet (CV) staining method was used to evaluate the growth. There were no differences in biofilm growth expressed as CV absorbance between C. albicans strains from different origins neither in Yeast Nitrogen Base broth (YNB) or in bovine serum (BS) (ANOVA, P=0.1648, P=0.5106, respectively). In the BS, the biofilm production was greater than in YNB medium for all samples (ANOVA, P=0.0003).
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Non-lipophilic mycobiota of human skin

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The human skin is inhabited by many species of bacteria and fungi, which are its natural microbiota. Fungi colonizing the skin, including those causing disease, characterized by great variety and variability, can be influenced by various factors. The purpose of this study was to investigate the composition of the non-lipiddependent fungal microbiota of skin, including the presence of species potentially pathogenic for humans. Fifty-six volunteers of both sexes aged 22–78 were subjected to the study. Swabs were taken from the face, chest, back and interdigital spaces of hands. Mycobiota isolated proved to vary both in terms of the location of occurrence and gender of patients. Interdigital spaces of hands, dominated by yeasts, constitute a location on human skin most contaminated with fungi. Molds were more often isolated from the face and chest. The back was the least contaminated location. There was no difference in fungal incidence in relation to sex.
A tracheotomy tube, as well as the stoma through which it is inserted into the patient’s throat, may represent a potential risk of fungal infections for patients suffering from larynx cancer. The study was aimed at evaluating the influence of the hospital room environment on the fungal colonisation of tracheotomy tubes in the case of patients diagnosed with larynx cancer and operated on in the Laryngology ward. The mycological research was carried out in the rooms of the Laryngology ward, from which 105 air samples were collected. Twenty-two Portex and metal tracheostomy tubes collected from 13 patients diagnosed with larynx cancer. Fungi were cultured on 15 tracheostomy tubes: moulds were isolated from 3 of these tubes, and fungi belonging to the genus Candida from the remaining 12. The simultaneous occurrence of the same moulds in the air and on the tracheotomy tubes was observed only in one case (Aspergillus flavus). In conclusion, the same moulds observed in the air can sometimes also be found on the tracheotomy tubes used by patients diagnosed with larynx cancer. Yeast-like fungi are isolated from tracheotomy tubes much more frequently than moulds, and this requires further mycological research.
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