Peer-Reviewed Journal Details
Mandatory Fields
Carberry, S;Molloy, E;Hammel, S;O'Keeffe, G;Jones, GW;Kavanagh, K;Doyle, S
2012
April
Fungal Genetics and Biology
Gliotoxin effects on fungal growth: Mechanisms and exploitation
Published
35 ()
Optional Fields
CU,ZN SUPEROXIDE-DISMUTASE BIOSYNTHETIC GENE-CLUSTER OXIDATIVE STRESS-RESPONSE MOUSE INFECTION MODEL ASPERGILLUS-FUMIGATUS TRANSCRIPTIONAL REGULATOR SACCHAROMYCES-CEREVISIAE GLUTATHIONE SYSTEM EXPRESSION
49
302
312
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 mu g/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 Delta gliT, lacking gliotoxin oxidoreductase, a gliotoxin self-protection gene. Saccharomyces cerevisiae deletents (Delta sod1 and Delta yap1) were hypersensitive to exogenous gliotoxin, while Delta gsh1 was resistant. Significant gliotoxin-mediated (5 mu g/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 mu g/ml), indicating differential gliotoxin sensitivity amongst fungi. Re-introduction of gliT into A. fumigatus Delta gliT, 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. (C) 2012 Elsevier Inc. All rights reserved.
SAN DIEGO
1087-1845
10.1016/j.fgb.2012.02.003
Grant Details