Furthermore, we can speculate that the exposure of clinically relevant moulds other than A. fumigatus to agricultural azoles may also be associated with the emergence of cross-resistance to clinical azoles. Several compounds are being tested in order to find new antifungal alternatives, anticipating the possible loss of efficacy of clinical azoles [21]. On the other hand, efforts should be made to find safer compounds to use in agriculture. Conclusions In order to NVP-AUY922 ic50 assess the real dimension of Aspergillus resistance,

a susceptibility test should be performed in all isolates from patients with Aspergillus infection. Moreover, for patients with severe infection initial combination therapy may be considered in geographical areas with high prevalence Selleckchem Napabucasin of environmental azole resistant isolates. Ultimately, surveillance studies in both clinical and in environment settings should be conducted in order to provide updated local data regarding susceptibility profiles. Methods Organisms Two clinical isolates of A. fumigatus, LMF05 and LMF11, and one environmental A. fumigatus isolate (LMN60, recovered from a garden

nearby the hospital), were click here used in this study. The isolates were identified as belonging to A. fumigatus species by macroscopic and microscopic morphology, the ability to grow at 48°C and by using MALDI-TOF MS to accurately discriminate A. fumigatus from a new sibling species A. lentulus, which cannot be distinguished by morphological characteristics or growth peculiarities [22]. Long-term preservation of conidial suspensions of the isolates was made in a GYEP medium (2% glucose, 0.3% yeast extract, 1% peptone) broth supplemented with 10% glycerol and stored at −80°C. Working cultures were subsequently maintained during 2 weeks on Sabouraud

dextrose agar slants and plates at 4°C. Antifungal agents and susceptibility profile PCZ is an imidazole and one of the main drugs used within European Union for crop protection [23]. This ergosterol biosynthesis inhibitor was selected as a representative of agricultural azoles after Methocarbamol a previous MIC screening, where it showed to be the less active agricultural drug on the selected strains, ie, it had the lower MIC values, which was a prerequisite for this induction experiment. Fluconazole (FLC), VRC, POS and ITZ were selected as clinical azoles. PCZ was ressuspended in 80% acetone solution at a final concentration of 5 mg/L. Clinical azoles were dissolved in dimethysulphoxide (DMSO) to obtain stock solutions of 10 mg/L. All drugs were stored at -20°C. Broth microdilution susceptibility assay was performed according to the Clinical and Laboratory Standards Institute M38-A2 protocol in order to evaluate the initial MIC of PCZ and of all the clinical azoles [24]. Drug concentration ranged from 0.125 to 64 mg/L of FLC and PCZ; and 0.