diamide and Aspergillosis

diamide has been researched along with Aspergillosis* in 2 studies

Other Studies

2 other study(ies) available for diamide and Aspergillosis

ArticleYear
Gliotoxin effects on fungal growth: mechanisms and exploitation.
    Fungal genetics and biology : FG & B, 2012, Volume: 49, Issue:4

    Although initially investigated for its antifungal properties, little is actually known about the effect of gliotoxin on Aspergillus fumigatus and other fungi. We have observed that exposure of A. fumigatus to exogenous gliotoxin (14 μg/ml), under gliotoxin-limited growth conditions, results in significant alteration of the expression of 27 proteins (up- and down-regulated >1.9-fold; p<0.05) including de novo expression of Cu, Zn superoxide dismutase, up-regulated allergen Asp f3 expression and down-regulated catalase and a peroxiredoxin levels. Significantly elevated glutathione GSH levels (p<0.05), along with concomitant resistance to diamide, were evident in A. fumigatus ΔgliT, lacking gliotoxin oxidoreductase, a gliotoxin self-protection gene. Saccharomyces cerevisiae deletents (Δsod1 and Δyap1) were hypersensitive to exogenous gliotoxin, while Δgsh1 was resistant. Significant gliotoxin-mediated (5 μg/ml) growth inhibition (p<0.001) of Aspergillus nidulans, Aspergillus terreus, Aspergillus niger, Cochliobolus heterostrophus and Neurospora crassa was also observed. Growth of Aspergillus flavus, Fusarium graminearum and Aspergillus oryzae was significantly inhibited (p<0.001) at gliotoxin (10 μg/ml), indicating differential gliotoxin sensitivity amongst fungi. Re-introduction of gliT into A. fumigatus ΔgliT, at a different locus (ctsD; AFUA_4G07040, an aspartic protease), with selection on gliotoxin, facilitated deletion of ctsD without use of additional antibiotic selection markers. Absence of ctsD expression was accompanied by restoration of gliT expression, and resistance to gliotoxin. Thus, we propose gliT/gliotoxin as a useful selection marker system for fungal transformation. Finally, we suggest incorporation of gliotoxin sensitivity assays into all future fungal functional genomic studies.

    Topics: Antifungal Agents; Ascomycota; Aspergillosis; Aspergillus; Aspergillus fumigatus; Biomarkers; Diamide; Down-Regulation; Fungal Proteins; Fusarium; Gene Expression Regulation, Fungal; Gliotoxin; Glutathione; Neurospora crassa; Oxidation-Reduction; Oxidoreductases; Saccharomyces cerevisiae; Sequence Deletion; Superoxide Dismutase; Up-Regulation

2012
The mitogen-activated protein kinase MpkA of Aspergillus fumigatus regulates cell wall signaling and oxidative stress response.
    Fungal genetics and biology : FG & B, 2008, Volume: 45, Issue:5

    Mitogen-activated protein kinase (MAPK) signaling pathways are involved in the regulation of various cellular responses in eukaryotes. In fungal pathogens they are of special interest because of their possible contribution to pathogenicity. Bioinformatic analysis of the genome of the most prevalent airborne human pathogenic fungus Aspergillus fumigatus, revealed the presence of four distinct MAPK-encoding genes. Here, we present the detailed functional analysis of one of these MAPKs, MpkA. Comparative analysis revealed similarities of MpkA with MAPKs involved in cell wall integrity signaling of other fungi. Accordingly, the analysis of mpkA deletion mutants revealed severe sensitivity of the mutants against cell wall active compounds, drastical alterations of the fungal morphology and increased resistance against oxidative stress. The expression of mpkA was induced by cell wall damaging conditions. Despite its involvement in cell wall signaling no influence on virulence of the deletion of mpkA was observed in a murine infection model.

    Topics: Animals; Antifungal Agents; Artificial Gene Fusion; Aspergillosis; Aspergillus fumigatus; Benzenesulfonates; beta-Galactosidase; Caffeine; Cell Wall; Congo Red; Diamide; Gene Deletion; Gene Expression Regulation, Fungal; Genes, Reporter; Genetic Complementation Test; Hydrogen Peroxide; Mice; Mice, Inbred BALB C; Mitogen-Activated Protein Kinases; Oxidants; Oxidative Stress; Signal Transduction; Sodium Dodecyl Sulfate; Survival Analysis; Virulence; Vitamin K 3

2008