002% benomyl (25% active ingredient; Hi-Yield Chemical Company, Bonham, TX) (Milner et al., 1991). Controls for these experiments were conidia on plates that were not irradiated (placed in the chamber, but covered with an aluminum foil barrier). After exposure, the plates were incubated for 48 h in the dark at 28 °C, and then observed at × 400 magnification for germination. Conidia were considered germinated when a germ tube visibly projected from the conidium (Milner et al., 1991). At least Etoposide solubility dmso 300 conidia per plate were evaluated, and the relative

percent germination was calculated as described by Braga et al. (2001). Two milliliters of the same filtered suspension used for UVB exposure was placed in pyrex screw-cap tubes (16 × 125 mm)

and placed immediately in a 45 °C agitated (stirred) waterbath (Rangel et al., 2005a, b). After 3 h of wet-heat exposure, 20 μL of the conidial suspension was inoculated (dropped, but not spread) onto PDAY+benomyl medium and germination was determined as described above and elsewhere (Rangel et al., 2005a, b). To measure GSK2126458 cost conidial production after a 14-day incubation under the different culture conditions, three agar plugs were removed from each plate at random places in the medium with a cork borer (5 mm diameter) and all three (total surface area ∼60 mm2) were placed in 1 mL of sterile Tween 80 (0.01% v/v). The conidia were suspended by vigorous vortexing, and conidial concentrations were determined by hemacytometer learn more counts. Each experiment was performed on three different dates, and each experiment used a new batch of cultures. Assessment of the effects on conidia of continuous light or dark during their production, i.e., mycelial growth and conidiation, on PDAY medium was compared with the effects on conidia produced on MM in continuous dark as to differences in (1) relative conidial germination after heat or UVB treatment or (2) conidial production by one-way anova in a randomized block design in which trials were blocks. Relative germination data were arcsine-square root transformed and conidial production data were log transformed

before analysis to better meet assumptions of normality and homogeneity of variance. Pairwise comparisons of means were controlled for experiment-wise type I error using the Tukey method at α=0.05. Computations were performed using the MIXED procedure in sas (SAS Institute Inc., 2002). In many organisms, preadaptation to one stress may induce cross-protection to other stresses. This was found to be true for insect-pathogenic fungi M. robertsii (Rangel et al., 2006a, b, 2008) and Beauveria bassiana (Liu et al., 2009). When M. robertsii conidia were produced under nutritive stress (carbon starvation) or osmotic stress (NaCl or KCl), they were approximately twofold more tolerant to heat and UVB radiation than conidia produced under normal conditions on a rich (PDAY) medium (Rangel et al.