Fig. 1. Example of indoor air uptake using air samplers in two different oak mushroom cultivation houses. A, log bed-based mushroom cultivation houses; B, sawdust media-based mushroom cultivation houses.
Fig. 2. Unrecorded fungal species isolated from mushroom cultivation houses in this study. The fungi were grown on potato dextrose agar at 25℃ for 7 days. A, Cenangium acuum; B, Periconia macrospinosa; C, Neopestalotiopsis surinamensis; D, Metarhizium marquandii; E, Trichoderma petersenii; F, Trichoderma paratroviride.
Fig. 3. Microscopic image of unrecorded fungal species isolated from mushroom cultivation houses in this study. A, Cenangium acuum; B, Periconia macrospinosa; C, Neopestalotiopsis surinamensis; D, Metarhizium marquandii; E, Trichoderma petersenii; F, Trichoderma paratroviride. Red arrow is important feature (scale bar = 2 μm).
Fig. 4-2. Phylogenic relationships of the six fungal isolates inferred by the neighbor joining analysis based on 28S rDNA (A), internal transcribed spacer rDNA (B, D), β-tubulin gene (C) or the translation elongation factor 1a gene (E, F) sequences. D, Metarhizium marquandii (NIBRFGC000499882); E, Trichoderma petersenii (NIBRFGC000499883); F, Trichoderma paratroviride (NIBRFGC000499884).
Fig. 4-2. Phylogenic relationships of the six fungal isolates inferred by the neighbor joining analysisbased on 28S rDNA (A), internal transcribed spacer rDNA (B, D), β-tubulin gene (C) or the translationelongation factor 1a gene (E, F) sequences. D, Metarhizium marquandii (NIBRFGC000499882); E,Trichoderma petersenii (NIBRFGC000499883); F, Trichoderma paratroviride (NIBRFGC000499884).
Table 1. List of the fungal species isolated and identifed in this study from mushroom cultivation houses in this study
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