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Background and Objective: Fungi are widely distributed in nature and they are usually present in attomospher but other sources such as water play an important role in their ecology. This study was done to evaluate mycoflora assessment in drinking tap water in Sari, North of Iran. The tap water collected form Sari water distribution system for fungi. Materials and Methods: In this descriptive study, a volume of 100 ml of tap drinking water samples (n=60) were collected in sterile bottles. All water samples passed through sterile 0.45 micrometer filters. The filters were placed directly on Malt extract agar and incubated at 27°C for 3-7 days. Routine mycological techniques were applied to identify the grown fungi. Results: Out of 468 grown fungal colonies, eight different fungal genera were identified. The total mean cfu per 100 ml for the positive samples were 8.4. Aspergillus (37.4%) and Penicillium (27.3%) were the most common isolated fungi. Rhizopus (0.6%) had the lowest frequency. Among Aspergillus species, A. flavus had the highest frequency. Conclusion: Our result showed that various fungi were present in the tap drinking water. We propose fungi should be considered as part of the microbiological analysis parameters in drinking tap water.

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Background and Objective: Fusarium solani is the common etiological agent of fungemia and disseminated fusariosis, which is associated with high incidence of mortality in immune-compromised host. Due to high level of resistance of antifungals in Fusarium solani, rapid and specific identification of organism is essential. This study was done to evaluate the PCR method for rapid and specific diagnosis of Fusarium solani in serum samples of HIV positive patients. Methods: In this descriptive study, the PCR test based on mitochondrial cytochrome b gene as the target gene with 330 bp product was optimized. PCR was applied on 45 serum samples of HIV positive patients after evaluation of sensitivity and specificity of the test. Results: In the optimized PCR test, the 330 bp product was amplified. The sensitivity of the test was a copy of Fusarium solani genome, and its specificity was 100%. Among 45 serum samples, 9 cases (20%) were positive for Fusarium solani. Conclusion: The PCR method has functional capabilities for direct, rapid and specific clinical diagnosis of Fusarium solani in HIV positive patients.

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Background and Objective: Trametes versicolor is important for its medicinal rather than nutritional value. Given the various pharmacological activities of this plant, this study aimed to investigate the antioxidant and antimicrobial potential of the aqueous extract of T. versicolor.
Methods: In this descriptive-analytical study, an aqueous extract of T. versicolor was prepared. Antioxidant activity, flavonoid content and total phenol were measured by diphenyl picryl hydrazyl (DPPH) and reducing power (RP) methods, aluminum chloride (AlCl3), and Folin-Ciocalteu assays. The antibacterial and antifungal activity of the aqueous extract of T. versicolor on Staphylococcus aureus, Escherichia coli and Fusarium thapsinum was determined by the disk diffusion method. Butylated hydroxytoluene (BHT), ciprofloxacin and amphotericin-B were used as positive controls for antioxidant activity and bacterial and fungal strains, respectively.
Results: Total phenolic content was 27.6±0.38 (mg GAE/g), and total flavonoid content was 4.2±0.04 (mg QE/g). Based on DPPH radical scavenging activity, the extract of T. versicolor showed strong scavenging activity (93.8±1.2 %) with IC50 of 103.9±0.8 μg/mL when compared with the standard BHT (IC50 of 30.0±0.6 μg/mL). In addition, it was observed that increasing the concentration of aqueous extract of turkey tail increased the reducing power of iron. The zone of inhibition around the extract ranged from 13.0±0.65 mm (in F. thapsinum at 75 mg/ml) to 21±0.73 mm (in S. aureus at 300 mg/ml) (P<0.05).
Conclusion: The aqueous extract of  T. versicolor contains a significant amount of phenolic compounds and also has strong antimicrobial and antioxidant properties.