The Cryptococcus neoformans STE12α gene, a homologue of Saccharomyces cerevisiae STE12, exists only in mating type (MAT)α cells. In S. cerevisiae, STE12 was required for mating and filament formation. In C. neoformans, haploid fruiting on filament agar required STE12α. The ability to form hyphae, however, was not affected by deletion of STE12α when convergently growing MATa strains were present. Furthermore, ste12α disruptants were fertile when mated with MATa strains, albeit with reduced mating frequency. Most importantly, the virulence of a ste12α disruptant of serotype D strain was significantly reduced in a mouse model. When the ste12α locus was reconstituted with the wild-type allele by cotransformation, virulence was restored. Histopathological analysis demonstrated a reduction in capsular size of yeast cells, less severe cystic lesions, and stronger immune responses in meninges of mice infected with ste12α cells than those of mice infected with STE12α cells. Using reporter gene constructs, we found that STE12α controls the expression of several phenotypes known to be involved in virulence, such as capsule and melanin production. These results demonstrate a clear molecular link between mating type and virulence in C. neoformans.
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6 March 2000
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March 06 2000
Cryptococcus neoformans STE12α Regulates Virulence but Is Not Essential for Mating
Y.C. Chang,
Y.C. Chang
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
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B.L. Wickes,
B.L. Wickes
cDepartment of Microbiology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78284
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G.F. Miller,
G.F. Miller
bVeterinary Resources Program, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
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L.A. Penoyer,
L.A. Penoyer
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
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K.J. Kwon-Chung
K.J. Kwon-Chung
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
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Y.C. Chang
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
B.L. Wickes
cDepartment of Microbiology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78284
G.F. Miller
bVeterinary Resources Program, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
L.A. Penoyer
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
K.J. Kwon-Chung
aLaboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Office of the Director, National Institutes of Health, Bethesda, Maryland 20892
Abbreviations used in this paper: GUS, β-glucuronidase; MAP, mitogen-activated protein; SLAD, synthetic low ammonia dextrose; YEPD, yeast extract peptone dextrose.
Received:
November 18 1999
Revision Requested:
January 07 2000
Accepted:
January 19 2000
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2000 government
2000
government
J Exp Med (2000) 191 (5): 871–882.
Article history
Received:
November 18 1999
Revision Requested:
January 07 2000
Accepted:
January 19 2000
Citation
Y.C. Chang, B.L. Wickes, G.F. Miller, L.A. Penoyer, K.J. Kwon-Chung; Cryptococcus neoformans STE12α Regulates Virulence but Is Not Essential for Mating. J Exp Med 6 March 2000; 191 (5): 871–882. doi: https://doi.org/10.1084/jem.191.5.871
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