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Sexual reproduction between partners of the same mating type in Cryptococcus neoformans

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Abstract

Cryptococcus neoformans is a globally distributed human fungal pathogen that causes life-threatening meningoencephalitis in immunocompromised patients1. It has a defined sexual cycle involving haploid cells of α and a mating types2, yet the vast majority of environmental and clinical isolates are α (ref. 3). Sexual recombination is normally expected to occur between isolates of opposite mating type in organisms with two mating types (or sexes). How sexual reproductive potential can be maintained in an organism with a largely unisexual, nearly clonal population genetic structure is unknown. One clue, however, is that α strains undergo fruiting, a process that resembles sexual mating4 but is thought to be strictly mitotic and asexual. We report here that hallmarks of mating occur during fruiting, including diploidization and meiosis. Pheromone response pathway elements and the key meiotic regulator Dmc1 are required for efficient fruiting. Furthermore, fusion and meiosis can occur between non-isogenic α strains, enabling genetic exchange. These studies reveal how sexual reproduction can occur between partners of the same mating type. These findings have implications for the evolution of microbial pathogens, as well as for parthenogenesis, cell fusion events and transitions between self-fertilizing and outcrossing modes of reproduction observed in both fungi and other kingdoms.

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Figure 1: Diploidization during monokaryotic fruiting.
Figure 2: Pheromone response and meiotic components promote fruiting.
Figure 3: Sexual recombination through mating or fruiting.

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References

  1. Casadevall, A. & Perfect, J. R. Cryptococcus neoformans (ASM Press, Washington, DC, 1998)

    Book  Google Scholar 

  2. Kwon-Chung, K. J. Morphogenesis of Filobasidiella neoformans, the sexual state of Cryptococcus neoformans. Mycologia 68, 821–833 (1976)

    Article  CAS  Google Scholar 

  3. Kwon-Chung, K. J. & Bennett, J. E. Distribution of α and a mating types of Cryptococcus neoformans among natural and clinical isolates. Am. J. Epidemiol. 108, 337–340 (1978)

    Article  CAS  Google Scholar 

  4. Wickes, B. L., Mayorga, M. E., Edman, U. & Edman, J. C. Dimorphism and haploid fruiting in Cryptococcus neoformans: association with the α-mating type. Proc. Natl Acad. Sci. USA 93, 7327–7331 (1996)

    Article  ADS  CAS  Google Scholar 

  5. Hull, C. M. & Heitman, J. Genetics of Cryptococcus neoformans. Annu. Rev. Genet. 36, 557–615 (2002)

    Article  CAS  Google Scholar 

  6. McClelland, C. M., Chang, Y. C., Varma, A. & Kwon-Chung, K. J. Uniqueness of the mating system in Cryptococcus neoformans. Trends Microbiol. 12, 208–212 (2004)

    Article  CAS  Google Scholar 

  7. Wang, P., Perfect, J. R. & Heitman, J. The G-protein β subunit GPB1 is required for mating and haploid fruiting in Cryptococcus neoformans. Mol. Cell. Biol. 20, 352–362 (2000)

    Article  Google Scholar 

  8. Shen, W. C., Davidson, R. C., Cox, G. M. & Heitman, J. Pheromones stimulate mating and differentiation via paracrine and autocrine signaling in Cryptococcus neoformans. Eukaryot. Cell 1, 366–377 (2002)

    Article  CAS  Google Scholar 

  9. Rose, M. D., Price, B. R. & Fink, G. R. Saccharomyces cerevisiae nuclear fusion requires prior activation by alpha factor. Mol. Cell. Biol. 6, 3490–3497 (1986)

    Article  CAS  Google Scholar 

  10. Hull, C. M., Davidson, R. C. & Heitman, J. Cell identity and sexual development in Cryptococcus neoformans are controlled by the mating-type-specific homeodomain protein Sxi1α. Genes Dev. 16, 3046–3060 (2002)

    Article  CAS  Google Scholar 

  11. Marra, R. E. et al. A genetic linkage map of Cryptococcus neoformans variety neoformans serotype D (Filobasidiella neoformans). Genetics 167, 619–631 (2004)

    Article  CAS  Google Scholar 

  12. Sauvageau, S., Ploquin, M. & Masson, J. Y. Exploring the multiple facets of the meiotic recombinase Dmc1. Bioessays 26, 1151–1155 (2004)

    Article  CAS  Google Scholar 

  13. Mitchell, A. P. & Herskowitz, I. Activation of meiosis and sporulation by repression of the RME1 product in yeast. Nature 319, 738–742 (1986)

    Article  ADS  CAS  Google Scholar 

  14. Thomas, C. F. Jr & Limper, A. H. Pneumocystis pneumonia. N. Engl. J. Med. 350, 2487–2498 (2004)

    Article  CAS  Google Scholar 

  15. Matsumoto, Y. & Yoshida, Y. Sporogony in Pneumocystis carinii: synaptonemal complexes and meiotic nuclear divisions observed in precysts. J. Protozool. 31, 420–428 (1984)

    Article  CAS  Google Scholar 

  16. Wyder, M. A., Rasch, E. M. & Kaneshiro, E. S. Quantitation of absolute Pneumocystis carinii nuclear DNA content. Trophic and cystic forms isolated from infected rat lungs are haploid organisms. J. Eukaryot. Microbiol. 45, 233–239 (1998)

    Article  CAS  Google Scholar 

  17. Smulian, A. G., Sesterhenn, T., Tanaka, R. & Cushion, M. T. The ste3 pheromone receptor gene of Pneumocystis carinii is surrounded by a cluster of signal transduction genes. Genetics 157, 991–1002 (2001)

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Shimizu, K. K. et al. Darwinian selection on a selfing locus. Science 306, 2081–2084 (2004)

    Article  ADS  CAS  Google Scholar 

  19. Johnson, A. The biology of mating in Candida albicans. Nature Rev. Microbiol. 1, 106–116 (2003)

    Article  ADS  CAS  Google Scholar 

  20. Grigg, M. E., Bonnefoy, S., Hehl, A. B., Suzuki, Y. & Boothroyd, J. C. Success and virulence in Toxoplasma as the result of sexual recombination between two distinct ancestries. Science 294, 161–165 (2001)

    Article  ADS  CAS  Google Scholar 

  21. Su, C. et al. Recent expansion of Toxoplasma through enhanced oral transmission. Science 299, 414–416 (2003)

    Article  ADS  CAS  Google Scholar 

  22. Anderson, J. B., Sirjusingh, C. & Ricker, N. Haploidy, diploidy and evolution of antifungal drug resistance in Saccharomyces cerevisiae. Genetics 168, 1915–1923 (2004)

    Article  CAS  Google Scholar 

  23. Galitski, T., Saldanha, A. J., Styles, C. A., Lander, E. S. & Fink, G. R. Ploidy regulation of gene expression. Science 285, 251–254 (1999)

    Article  CAS  Google Scholar 

  24. Zeyl, C., Vanderford, T. & Carter, M. An evolutionary advantage of haploidy in large yeast populations. Science 299, 555–558 (2003)

    Article  ADS  CAS  Google Scholar 

  25. Zeyl, C. Experimental studies on ploidy evolution in yeast. FEMS Microbiol. Lett. 233, 187–192 (2004)

    Article  CAS  Google Scholar 

  26. Vassilopoulos, G., Wang, P. R. & Russell, D. W. Transplanted bone marrow regenerates liver by cell fusion. Nature 422, 901–904 (2003)

    Article  ADS  CAS  Google Scholar 

  27. Kwon-Chung, K. J., Edman, J. C. & Wickes, B. L. Genetic association of mating types and virulence in Cryptococcus neoformans. Infect. Immun. 60, 602–605 (1992)

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Sia, R. A., Lengeler, K. B. & Heitman, J. Diploid strains of the pathogenic basidiomycete Cryptococcus neoformans are thermally dimorphic. Fungal Genet. Biol. 29, 153–163 (2000)

    Article  CAS  Google Scholar 

  29. Fraser, J. A., Subaran, R. L., Nichols, C. B. & Heitman, J. Recapitulation of the sexual cycle of the primary fungal pathogen Cryptococcus neoformans var. gattii: implications for an outbreak on Vancouver Island, Canada. Eukaryot. Cell 2, 1036–1045 (2003)

    Article  CAS  Google Scholar 

  30. Toffaletti, D. L., Rude, T. H., Johnston, S. A., Durack, D. T. & Perfect, J. R. Gene transfer in Cryptococcus neoformans by use of biolistic delivery of DNA. J. Bacteriol. 175, 1405–1411 (1993)

    Article  CAS  Google Scholar 

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Acknowledgements

We thank W.-C. Shen for strains, A. Mitchell, J. Fraser and A. Idnurm for discussions, and T. Mitchell, D. Lew, B. Capel, R. Wharton and J. Anderson for critical reading. This work was supported by an NIAID R01 grant to J.H. C.M.H. was supported by a Damon Runyon Cancer Research Fellowship and a Burroughs Wellcome Career Development Award in the Biomedical Sciences. J.H. is a Burroughs Wellcome Fund Scholar in Molecular Pathogenic Mycology and an Investigator of the Howard Hughes Medical Institute.

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Correspondence to Xiaorong Lin or Joseph Heitman.

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Supplementary Notes

This file contains Supplementary Data, Supplementary Methods, Supplementary Figure Legend and additional references. (DOC 41 kb)

Supplementary Figure S1

Dikaryotic mating hyphae contain two nuclei per compartment that alternate position at each conjugate division. (PDF 23 kb)

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Lin, X., Hull, C. & Heitman, J. Sexual reproduction between partners of the same mating type in Cryptococcus neoformans. Nature 434, 1017–1021 (2005). https://doi.org/10.1038/nature03448

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