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2004 | 11 | 1 |

Tytuł artykułu

Airway toxicity of house dust and its fungal composition

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
House dust is an important source of different toxic metabolites as well as allergens, including those of fungal origin, in the indoor environment. A bio-assay employing 1-day-old chick tracheas was used to characterize airway effects of 2-butanone and dimethylsulphoxide (Me2SO) extracts of 23 dust samples collected from water damaged (13) and control (10) Danish schools. Direct microscopical analysis of samples, followed by cultivation on dichloran 18% glycerol agar at 25oC for 10 days to establish their mycoflora, was performed. The in vitro ciliostatic potential of the chloroform-extractable endo- and exometabolites of 41 representative fungal isolates was determined. Nine dust extracts in 2-butanone (2 from damp rooms) or 10 (6) in Me2SO showed some ciliostatic activity in the 3-days' experiment. Fungal composition of dust from buildings with leakage was almost identical with that from undamaged houses, as well as the fungal colony counts from the damp schools and the control samples. Aspergillus spp. were prevalent in the samples - 31 or 40% of all fungi, followed by Penicillium spp. and Cladosporium cladosporioides. Alternaria spp., Chaetomium spp., Mucor spp., Mycelia sterilia, Paecilomyces variotii, Rhizopus sp., Ulocladium sp. and yeasts were each isolated in less than 8% of the fungal content. No Aspergillus flavus isolate (8 in total) was aflatoxigenic ,em>in vitro. Alternaria spp., Aspergillus spp., Botrytis cinerea, Penicillium spp., C. cladosporioides, Chaetomium spp. and Ulocladium sp.; in total, 88% of all fungi tested, produced ciliostatically active metabolites. These toxigenic strains were also present in 4 dust samples from controls and 5 dust samples from water damaged buildings. Extracts of these dust samples were also toxic in bioassay. There were bio-detectable concentrations (10-20 µg of extracts/ml of the organ culture medium) of toxic compounds in house dust. Contribution of fungal metabolites to its toxic effect should be studied further.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

11

Numer

1

Opis fizyczny

p.67-73,fig.,ref.

Twórcy

autor
  • Slovak Medical University, Limbova 12, SK-813 03 Bratislava, Slovakia
autor

Bibliografia

  • 1. Abarca M, Bragualat MR, Bruguera MT, Cabanes FJ: Comparison of some screening methods for testing aflatoxigenic moulds. Mycopathol 1988, 104, 75-79.
  • 2. Bahkali AH, Parvez S: Fungal flora in house dust in Ryiadh, Saudi Arabia. Mycoses 1999, 42, 339-343.
  • 3. Douwes J, van der Sluis B, Doekes G, van Leusden F, Wijnands L, van Strien R, Verhoeff A, Brunekreef B: Fungal extracellular polysaccharides in house dust as a marker for exposure to fungi: Relations with culturable fungi, reported home dampness, and respiratory symptoms. J Allergy Clin Immunol 1999, 103, 494-500.
  • 4. Engelhart S, Loock A, Skutlarek D, Sagunski H, Lommel A, Farber H, Exner M: Occurrence of toxigenic Aspergillus versicolor isolates and sterigmatocystin in carpet dust from damp indoor environments. Appl Environ Microbiol 2002, 68, 3886-3890.
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  • 6. Gross I, Heinrich J, Fahlbusch B: Standardization of house-dust sampling. Allergol 1997, 20, 449-456.
  • 7. Jesenská Z, Bernát D: Effects of mycotoxins on in vitro movement of tracheal cilia from one-day-old chicks. Folia Microbiol 1994, 39, 155-158.
  • 8. Kalliokoski P, Pasanen AL, Korpi A, Pasanen P: House dust as a growth medium for microorganisms. In: Proceedings of Indoor Air’96, 131-135. Seec Ishibashi Inc., Tokyo 1996.
  • 9. Korpi A, Pasanen AL, Pasanen P, Kalliokoski P: Microbial growth and metabolism in house dust. Int Biodeter Biodegrad 1997, 40, 19-27.
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  • 11. Pasanen P, Korpi A, Kalliokoski P, Pasanen AL: Growth and volatile metabolite production of Aspergillus versicolor in house dust. Environ Int 1997, 23, 425-432.
  • 12. Piecková E: In vitro toxicity of indoor Chaetomium Kunze ex Fr. Ann Agric Environ Med 2003, 10, 9-14.
  • 13. Piecková E, Jesenská Z: Microscopic fungi in dwellings and their health implications in humans. Ann Agric Environ Med 1999, 6, 1-11.
  • 14. Piecková E, Kunová Z: Indoor fungi and their ciliostatic metabolites. Ann Agric Environ Med 2002, 9, 59-63.
  • 15. Ren P, Jankun TJ, Leaderer BP: Comparisons of seasonal fungal prevalence in indoor and outdoor air and in house dusts of dwellings in one Northeast American county. J Exp Anal Environ Epidemiol 1999, 9, 560-568.
  • 16. Roberts JW, Clifford WS, Glass G, Hummer PG: Reducing dust, lead, dust mites, bacteria, and fungi in carpets by vacuuming. Arch Environ Contam Toxicol 1999, 36, 477-484.
  • 17. Saraf A, Larsson L, Burge H, Milton D: Quantification of ergosterol and 3-hydroxy fatty acids in settled house dust by gas chromatographymass spectrometry: comparison with fungal culture and determination of endotoxin by a Limulus amebocyte lysate assay. Appl Enviorn Microbiol 1997, 63, 2554-2559.
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Typ dokumentu

Bibliografia

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