Institut für Molekulare Infektionsbiologie, Universität Würzburg, Josef-Schneider-Str. 2, Würzburg, Germany.
Med Microbiol Immunol. 2010 Aug;199(3):165-72. doi: 10.1007/s00430-010-0147-0.
The yeast Candida albicans is part of the microflora in most healthy people, but can become a pathogen when host defenses are compromised. The phenotypic plasticity of C. albicans, which includes switching between different morphologies, contributes to its ability to colonize and infect virtually all body locations. A particularly fascinating developmental program is white-opaque switching, a reversible transition between the normal yeast morphology (white) and an elongated cell type (opaque), which is the mating-competent form of this fungus. Although opaque cells are much less able than white cells to cause a systemic infection, they are better adapted for colonization of specific host niches, like skin. White-opaque switching is controlled by the mating type locus (MTL), which in most C. albicans strains exists in two alleles, MTLa and MTL. These strains produce a heterodimeric repressor, a1-alpha2, which suppresses switching to the opaque phase by inhibiting expression of the master regulator Wor1. Loss of MTL heterozygosity relieves this repression, a mechanism that ensures that only MTL homozygous cells can switch to the mating-competent opaque form. Several transcriptional feedback loops, including positive autoregulation of Wor1, result in bistable expression of the master regulator (low in white and high in opaque cells) and epigenetic inheritance of the two phases. White-opaque switching occurs stochastically at a low frequency, but certain environmental conditions can drive the switch from one phase to the other by affecting either the activity of the transcriptional feedback loops or accumulation of Wor1 protein in a cell. Such environmental regulation of phenotypic switching may restrict mating to suitable host niches, while allowing a C. albicans population to withstand the various challenges encountered in different tissues.
白色念珠菌是大多数健康人体内微生物群的一部分,但当宿主防御功能受损时,它可能成为病原体。白色念珠菌的表型可塑性,包括在不同形态之间的转换,有助于其在几乎所有身体部位定植和感染的能力。一个特别迷人的发育程序是白-暗转换,这是一种从正常酵母形态(白色)到伸长细胞类型(暗)的可逆转换,是这种真菌的有性繁殖形式。尽管暗细胞比白细胞更难以引起全身性感染,但它们更适应于特定宿主小生境的定植,如皮肤。白-暗转换受交配型基因座(MTL)控制,在大多数白色念珠菌菌株中,该基因座存在两个等位基因,MTLa 和 MTL。这些菌株产生一个异二聚体抑制剂 a1-alpha2,通过抑制主调控因子 Wor1 的表达来抑制向暗相的转换。失去 MTL 杂合性会解除这种抑制,这一机制确保只有 MTL 纯合细胞才能转换为有性繁殖能力的暗相。几个转录反馈回路,包括 Wor1 的正自调控,导致主调控因子的双稳态表达(在白色细胞中低,在暗细胞中高)和两个相的表观遗传遗传。白色-暗转换以低频率随机发生,但某些环境条件可以通过影响转录反馈回路的活性或 Wor1 蛋白在细胞中的积累来驱动从一个相到另一个相的转换。这种表型转换的环境调节可能会将交配限制在合适的宿主小生境中,同时允许白色念珠菌种群在不同组织中遇到的各种挑战中生存。