Unisexual reproduction in the global human fungal pathogen Cryptococcus neoformans

Sexual reproduction is a central tenet of the eukaryotic life cycle, essential for the long-term survival of a species. Sex promotes genetic diversity and facilitates natural selection, and in eukaryotes such as unicellular fungi, sexual reproduction leads to hyphal growth and spore production, enabling escape from harsh environments and long-distance dispersal. The human fungal pathogen Cryptococcus species complex (encompassing C. neoformans , C. deneoformans , and the C. gattii sub-complexes) exhibit diversity in sexual reproduction, including α- a mating, pseudosexual reproduction, as well as unisexual reproduction initiated from a single isolate or between isolates of the same mating type. A central conundrum is that while most Cryptococcus natural populations exhibit significant α mating type bias, genetic and genomic analyses show recombination occurs in nature. The discovery of unisexual reproduction in C. deneoformans provided insight; however, thus far unisexual reproduction has never been observed in the predominant global pathogenic species C. neoformans . Here, we provide evidence that mutating the RIC8 gene, which encodes a conserved guanine nucleotide exchange factor (GEF) involved in activation of Gα proteins, enables unisexual reproduction in C. neoformans . Additionally, we show that genetic variation in the natural population promotes unisexual reproduction, and unisexual reproduction in C. neoformans shares similarities with that in C. deneoformans and involves canonical meiotic recombination. Finally, our data suggest that Ric8 interacts with Gpa1 and Gpa2 during α- a mating, but the localization of these Gα proteins is not influenced by Ric8 during unisexual reproduction. This suggests differential regulation of the Gα proteins, likely involving the Ric8 protein, could underly switch between different modes of sexual reproduction in Cryptococcus . Our study further highlights that the highly conserved Ric8 GEF can act as an important regulator of cellular development in response to environmental stimuli and modulates sexual reproduction in nature. We hypothesize that unisexual reproduction occurs much more frequently in nature than currently appreciated, and possibly in other fungal species as well.