TY - JOUR
T1 - GliZ, a transcriptional regulator of gliotoxin biosynthesis, contributes to Aspergillus fumigatus virulence
AU - Bok, Jin Woo
AU - Chung, Da Woon
AU - Balajee, S. Arunmozhi
AU - Marr, Kieren A.
AU - Andes, David
AU - Nielsen, Kristian Fog
AU - Frisvad, Jens C.
AU - Kirby, Katharine A.
AU - Keller, Nancy P.
PY - 2006/12
Y1 - 2006/12
N2 - Gliotoxin is a nonribosomal peptide produced by Aspergillus fumigatus. This compound has been proposed as an A. fumigatus virulence factor due to its cytotoxic, genotoxic, and apoptotic properties. Recent identification of the gliotoxin gene cluster identified several genes (gli genes) likely involved in gliotoxin production, including gliZ, encoding a putative Zn2Cys 6 binuclear transcription factor. Replacement of gliZ with a marker gene (ΔgliZ) resulted in no detectable gliotoxin production and loss of gene expression of other gli cluster genes. Placement of multiple copies of gliZ in the genome increased gliotoxin production. Using endpoint survival data, the ΔgliZ and a multiple-copy gliZ strain were not statistically different from the wild type in a murine pulmonary model; however, both the wild-type and the multiple-copy gliZ strain were more virulent than ΔlaeA (a mutant reduced in production of gliotoxin and other toxins). A flow-cytometric analysis of polymorphonuclear leukocytes (PMNs) exposed to supernatants from wild-type, ΔgliZ, complemented ΔgliZ, and ΔlaeA strains supported a role for gliotoxin in apoptotic but not necrotic PMN cell death. This may indicate that several secondary metabolites are involved in A. fumigatus virulence.
AB - Gliotoxin is a nonribosomal peptide produced by Aspergillus fumigatus. This compound has been proposed as an A. fumigatus virulence factor due to its cytotoxic, genotoxic, and apoptotic properties. Recent identification of the gliotoxin gene cluster identified several genes (gli genes) likely involved in gliotoxin production, including gliZ, encoding a putative Zn2Cys 6 binuclear transcription factor. Replacement of gliZ with a marker gene (ΔgliZ) resulted in no detectable gliotoxin production and loss of gene expression of other gli cluster genes. Placement of multiple copies of gliZ in the genome increased gliotoxin production. Using endpoint survival data, the ΔgliZ and a multiple-copy gliZ strain were not statistically different from the wild type in a murine pulmonary model; however, both the wild-type and the multiple-copy gliZ strain were more virulent than ΔlaeA (a mutant reduced in production of gliotoxin and other toxins). A flow-cytometric analysis of polymorphonuclear leukocytes (PMNs) exposed to supernatants from wild-type, ΔgliZ, complemented ΔgliZ, and ΔlaeA strains supported a role for gliotoxin in apoptotic but not necrotic PMN cell death. This may indicate that several secondary metabolites are involved in A. fumigatus virulence.
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U2 - 10.1128/IAI.00780-06
DO - 10.1128/IAI.00780-06
M3 - Article
C2 - 17030582
AN - SCOPUS:33845507811
SN - 0019-9567
VL - 74
SP - 6761
EP - 6768
JO - Infection and immunity
JF - Infection and immunity
IS - 12
ER -