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. 2017 May 8;12(5):e0177099. doi: 10.1371/journal.pone.0177099

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© 2017 Park et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 3 — (A) Viability of the conidia of WT (FGSC4), ΔvadA (THS33.1), and C’ (THS34.1) strains grown at 37°C for 5 and 10 days (** P < 0.01). (B) Amount of trehalose per 10⁷ conidia in the two-day-old conidia of WT (FGSC4), ΔvadA (THS33.1), and C’ (THS34.1) strains (measured in triplicate) (*** P < 0.001). (C) Tolerance of the conidia of WT (FGSC4), ΔvadA (THS33.1), and C’ (THS34.1) strains to H₂O₂ treatment. (D) Amount of β-glucan (pg) per 10³ conidia in the two-day-old conidia of WT (FGSC4), ΔvadA (THS33.1), and C’ (THS34.1) strains (measured in triplicate). (E) Levels of vadA, brlA, wetA, tpsA, orlA, rodA, and fksA transcripts in the conidia of WT (FGSC4), ΔvadA (THS33.1), and C’ (THS34.1) strains. Equal loading of total RNA was confirmed by ethidium bromide staining of rRNA.