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Isolation and Characterization of Cryptococcus Neoformans Spores Reveal a Critical Role for Capsule Biosynthesis Genes in Spore Biogenesis

Overview
Journal Eukaryot Cell
Specialty Molecular Biology
Date 2009 Feb 3
PMID 19181873
Citations 55
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Abstract

Spores are essential particles for the survival of many organisms, both prokaryotic and eukaryotic. Among the eukaryotes, fungi have developed spores with superior resistance and dispersal properties. For the human fungal pathogens, however, relatively little is known about the role that spores play in dispersal and infection. Here we present the purification and characterization of spores from the environmental fungus Cryptococcus neoformans. For the first time, we purified spores to homogeneity and assessed their morphological, stress resistance, and surface properties. We found that spores are morphologically distinct from yeast cells and are covered with a thick spore coat. Spores are also more resistant to environmental stresses than yeast cells and display a spore-specific configuration of polysaccharides on their surfaces. Surprisingly, we found that the surface of the spore reacts with antibodies to the polysaccharide glucuronoxylomannan, the most abundant component of the polysaccharide capsule required for C. neoformans virulence. We explored the role of capsule polysaccharide in spore development by assessing spore formation in a series of acapsular strains and determined that capsule biosynthesis genes are required for proper sexual development and normal spore formation. Our findings suggest that C. neoformans spores may have an adapted cell surface that facilitates persistence in harsh environments and ultimately allows them to infect mammalian hosts.

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References
1.
Wickes B, Edman U, Edman J . The Cryptococcus neoformans STE12alpha gene: a putative Saccharomyces cerevisiae STE12 homologue that is mating type specific. Mol Microbiol. 1998; 26(5):951-60. DOI: 10.1046/j.1365-2958.1997.6322001.x. View

2.
Kwon-Chung K . A new genus, filobasidiella, the perfect state of Cryptococcus neoformans. Mycologia. 1975; 67(6):1197-200. View

3.
Briza P, Breitenbach M, Ellinger A, Segall J . Isolation of two developmentally regulated genes involved in spore wall maturation in Saccharomyces cerevisiae. Genes Dev. 1990; 4(10):1775-89. DOI: 10.1101/gad.4.10.1775. View

4.
Arrage A, Phelps T, Benoit R, White D . Survival of subsurface microorganisms exposed to UV radiation and hydrogen peroxide. Appl Environ Microbiol. 1993; 59(11):3545-50. PMC: 182496. DOI: 10.1128/aem.59.11.3545-3550.1993. View

5.
Lin X, Hull C, Heitman J . Sexual reproduction between partners of the same mating type in Cryptococcus neoformans. Nature. 2005; 434(7036):1017-21. DOI: 10.1038/nature03448. View