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Wyszukujesz frazę "Indoor air fungi" wg kryterium: Wszystkie pola


Wyświetlanie 1-2 z 2
Tytuł:
The capability of fungi isolated from moldy dwellings to produce toxins
Autorzy:
Jeżak, Karolina
Kozajda, Anna
Sowiak, Małgorzata
Brzeźnicki, Sławomir
Bonczarowska, Marzena
Szadkowska-Stańczyk, Irena
Powiązania:
https://bibliotekanauki.pl/articles/2168358.pdf
Data publikacji:
2016-07-27
Wydawca:
Instytut Medycyny Pracy im. prof. dra Jerzego Nofera w Łodzi
Tematy:
indoor air
mycotoxins
molds
residential environment
sterigmatocystin
roquefortine C
Opis:
Objectives The main objective was analysis and assessment of toxinogenic capabilities of fungi isolated from moldy surfaces in residential rooms in an urban agglomeration situated far from flooded areas in moderate climate zone. Material and Methods The assessment of environmental exposure to mycotoxins was carried out in samples collected from moldy surfaces in form of scrapings and airborne dust from 22 moldy dwellings in winter season. In each sample 2 mycotoxins were analyzed: sterigmatocystin and roquefortine C produced by Aspergillus versicolor and Penicillium chrysogenum, respectively. Mycotoxins were analyzed by high-performance liquid chromatography (HPLC) in: scrapings from moldy surfaces, mixture of all species of fungi cultured from scrapings on microbiological medium (malt extract agar), pure cultures of Aspergillus versicolor and Penicillium chrysogenum cultured from scrapings on microbiological medium; mycotoxins in the indoor air dust were also analyzed. Results The production of sterigmatocystin by individual strains of Aspergillus versicolor cultured on medium was confirmed for 8 of 13 isolated strains ranging 2.1–235.9 μg/g and production of roquefortine C by Penicillium chrysogenum for 4 of 10 strains ranging 12.9–27.6 μg/g. In 11 of 13 samples of the mixture of fungi cultured from scrapings, in which Aspergillus versicolor was found, sterigmatocystin production was at the level of 3.1–1683.2 μg/g, whereas in 3 of 10 samples in which Penicillium chrysogenum occurred, the production of roquefortine C was 0.9–618.9 μg/g. The analysis did not show in any of the tested air dust and scrapings samples the presence of analyzed mycotoxins in the amount exceeding the determination limit. Conclusions The capability of synthesis of sterigmatocystin by Aspergillus versicolor and roquefortine C by Penicillium chrysogenum growing in mixtures of fungi from scrapings and pure cultures in laboratory conditions was confirmed. The absence of mycotoxins in scrapings and air dust samples indicates an insignificant inhalatory exposure to mycotoxins among inhabitants in moldy flats of urban agglomeration situated far from flooded territories. Int J Occup Med Environ Health 2016;29(5):823–836
Źródło:
International Journal of Occupational Medicine and Environmental Health; 2016, 29, 5; 823-836
1232-1087
1896-494X
Pojawia się w:
International Journal of Occupational Medicine and Environmental Health
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Assessment of exposure to fungi in the heavily contaminated work environment (a solid waste sorting plant) based on the ergosterol analysis
Autorzy:
Kozajda, Anna I.
Jeżak, Karolina
Sowiak, Małgorzata
Gutarowska, Beata
Szadkowska-Stańczyk, Irena
Powiązania:
https://bibliotekanauki.pl/articles/2177184.pdf
Data publikacji:
2015-07-17
Wydawca:
Instytut Medycyny Pracy im. prof. dra Jerzego Nofera w Łodzi
Tematy:
occupational exposure
bioaerosols
sterols
solid waste management plant
ergosterol
indoor air pollution
Opis:
Objectives This paper reports on the results of the study aimed at application of ergosterol as an quantitative indicator of fungal bioaerosol present in the indoor air in occupational environment heavily contaminated with organic dust as well as its comparison with the culturable method. Material and Methods The study was conducted in the indoor solid waste sorting plant. Using Andersen impactor adapted to 1 plate at the flow rate of 30 l/min, indoor air was sampled in the workers’ breathing zone. Ergosterol was sampled using gelatinous filter (1000 l of air) and then analyzed by means of the spectrophotometric method. Fungi were sampled on malt extract agar (MEA) medium (3 replications: 2 l, 7.5 l, 15 l of air) and analyzed by means of the culturable method. Based on ergosterol analyzes, concentration of fungi was calculated. Results were given as the range assuming min. as 5.1 pg ergosterol/spore and max as 1.7 pg ergosterol/spore. Results The average concentrations of ergosterol in a working room (arithmetic mean (AM), standard deviation (SD); minimum–maximum (min.–max)) were, respectively: 2.16, 0.72; 0.85–2.92 μg/m³; fungi calculated based on ergosterol – 424.1×10³–1272.4×10³, 140.1×10³– 420.4×10³, 167×10³–1716.5×10³ CFU/m³, and culturable fungi – 13×10³, 9.7×10³, 1.9×10³–34×10³ CFU/m³). It was revealed that concentrations of calculated fungi were even 2 orders of magnitude higher than culturable fungi. Conclusions The quantitative assessment of moldiness by means of ergosterol measurement seems to be a reliable indicator for environments heavily contaminated with organic dust, where viable and non-viable fungi are present in high proportions. Based on that result, more restrictive (as compared to a similar assessment carried out by means of the culturable method) hygienic recommendations, especially those related to the use of preventive measures protecting the employees’ respiratory tract, should have been undertaken.
Źródło:
International Journal of Occupational Medicine and Environmental Health; 2015, 28, 5; 813-821
1232-1087
1896-494X
Pojawia się w:
International Journal of Occupational Medicine and Environmental Health
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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