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  • Review Article
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Interspecific hybridization as a driver of fungal evolution and adaptation

Abstract

Cross-species gene transfer is often associated with bacteria, which have evolved several mechanisms that facilitate horizontal DNA exchange. However, the increased availability of whole-genome sequences has revealed that fungal species also exchange DNA, leading to intertwined lineages, blurred species boundaries or even novel species. In contrast to prokaryotes, fungal DNA exchange originates from interspecific hybridization, where two genomes are merged into a single, often highly unstable, polyploid genome that evolves rapidly into stabler derivatives. The resulting hybrids can display novel combinations of genetic and phenotypic variation that enhance fitness and allow colonization of new niches. Interspecific hybridization led to the emergence of important pathogens of humans and plants (for example, various Candida and ‘powdery mildew’ species, respectively) and industrially important yeasts, such as Saccharomyces hybrids that are important in the production of cold-fermented lagers or cold-cellared Belgian ales. In this Review, we discuss the genetic processes and evolutionary implications of fungal interspecific hybridization and highlight some of the best-studied examples. In addition, we explain how hybrids can be used to study molecular mechanisms underlying evolution, adaptation and speciation, and serve as a route towards development of new variants for industrial applications.

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Fig. 1: Occurrence of interspecific hybridization in fungi.
Fig. 2: Road map to overcoming species boundaries.
Fig. 3: Genome stabilization after hybridization.
Fig. 4: Transcriptional response to hybridization.
Fig. 5: Assembly of protein complexes in fungal interspecific hybrids.

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References

  1. Griffith, F. The significance of pneumococcal types. J. Hyg. 27, 113–159 (1928).

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Sun, D. Pull in and push out: mechanisms of horizontal gene transfer in bacteria. Front. Microbiol. 9, 2154 (2018).

    PubMed  PubMed Central  Google Scholar 

  3. Riley, M. A. & Lizotte-Waniewski, M. Population genomics and the bacterial species concept. Methods Mol. Biol. 532, 367–377 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Soltis, D. E., Visger, C. J. & Soltis, P. S. The polyploidy revolution then…and now: Stebbins revisited. Am. J. Bot. 101, 1057–1078 (2014).

    PubMed  Google Scholar 

  5. Stebbins, G. The role of hybridization in evolution. Proc. Am. Philos. Soc. 103, 231–251 (1959).

    Google Scholar 

  6. Hübner, S. et al. Sunflower pan-genome analysis shows that hybridization altered gene content and disease resistance. Nat. Plants 5, 54–62 (2019).

    PubMed  Google Scholar 

  7. Lamichhaney, S. et al. Rapid hybrid speciation in Darwin’s finches. Science 359, 224–228 (2018).

    CAS  PubMed  Google Scholar 

  8. Edelman, N. B. et al. Genomic architecture and introgression shape a butterfly radiation. Science 366, 594–599 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Mixão, V. & Gabaldón, T. Hybridization and emergence of virulence in opportunistic human yeast pathogens. Yeast 35, 5–20 (2018). In this review, the authors comprehensively discuss how hybridization can influence the origin and evolution of pathogenic fungal lineages.

    PubMed  Google Scholar 

  10. Gallone, B. et al. Interspecific hybridization facilitates niche adaptation in beer yeast. Nat. Ecol. Evol. 3, 1562–1575 (2019).

    PubMed  Google Scholar 

  11. Möller, M. & Stukenbrock, E. H. Evolution and genome architecture in fungal plant pathogens. Nat. Rev. Microbiol. 15, 756–771 (2017).

    PubMed  Google Scholar 

  12. Kominek, J. et al. Eukaryotic acquisition of a bacterial operon. Cell 176, 1356–1366.e10 (2019). In this article, the authors identify a case of adaptive ‘horizontal operon transfer’ from bacteria to fungi, which (after selection to facilitate gene expression) led to efficient iron scavenging.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Routh, A., Domitrovic, T. & Johnson, J. E. Host RNAs, including transposons, are encapsidated by a eukaryotic single-stranded RNA virus. Proc. Natl Acad. Sci. USA 109, 1907–1912 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Lee, S. C., Ni, M., Li, W., Shertz, C. & Heitman, J. The evolution of sex: a perspective from the fungal kingdom. Microbiol. Mol. Biol. Rev. 72, 298–340 (2010).

    Google Scholar 

  15. Idnurm, A., James, T. Y. & Vilgalys, R. Sex in the rest: mysterious mating in the Chytridiomycota and Zygomycota. in Sex in Fungi 405–418 (ASM Press, 2007).

  16. Coelho, M. A., Bakkeren, G., Sun, S., Hood, M. E. & Giraud, T. Fungal sex: basidiomycota. Fungal Kingd. 5, 147–175 (2017).

    Google Scholar 

  17. Clutterbuck, A. J. Parasexual recombination in fungi. J. Genet. 75, 281–286 (1996).

    Google Scholar 

  18. Bennett, R. J. The parasexual lifestyle of Candida albicans. Curr. Opin. Microbiol. 28, 10–17 (2015).

    PubMed  PubMed Central  Google Scholar 

  19. Anderson, J. B. et al. Determinants of divergent adaptation and Dobzhansky-Muller interaction in experimental yeast populations. Curr. Biol. 20, 1383–1388 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Mallet, J. Hybridization, ecological races and the nature of species: empirical evidence for the ease of speciation. Philos. Trans. R. Soc. B Biol. Sci. 363, 2971–2986 (2008).

    Google Scholar 

  21. D’Angiolo, M. et al. A yeast living ancestor reveals the origin of genomic introgressions. Nature 587, 420–425 (2020). This article shows how genome instability during mitotic growth of hybrid populations can lead to introgresssions and how this process over time can restore fertility.

    PubMed  Google Scholar 

  22. Kiss, L. et al. Temporal isolation explains host-related genetic differentiation in a group of widespread mycoparasitic fungi. Mol. Ecol. 20, 1492–1507 (2011).

    PubMed  Google Scholar 

  23. Greig, D. & Leu, J. Y. Natural history of budding yeast. Curr. Biol. 19, R886–R890 (2009).

    CAS  PubMed  Google Scholar 

  24. Giraud, T., Yockteng, R., López-Villavicencio, M., Refrégier, G. & Hood, M. E. Mating system of the anther smut fungus Microbotryum violaceum: selfing under heterothallism. Eukaryot. Cell 7, 765–775 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. Karlsson, M., Nygren, K. & Johannesson, H. The evolution of the pheromonal signal system and its potential role for reproductive isolation in heterothallic. Neurospora. Mol. Biol. Evol. 25, 168–178 (2007).

    PubMed  Google Scholar 

  26. Grabenstein, K. C. & Taylor, S. A. Breaking barriers: causes, consequences, and experimental utility of human-mediated hybridization. Trends Ecol. Evol. 33, 198–212 (2018).

    PubMed  Google Scholar 

  27. Scheele, B. C. et al. Amphibian fungal panzootic causes catastrophic and ongoing loss of biodiversity. Science 363, 1459–1463 (2019).

    CAS  PubMed  Google Scholar 

  28. Fisher, M. et al. Emerging fungal threats to animal, plant and ecosystem health. Nature 484, 186–194 (2012).

    CAS  PubMed  Google Scholar 

  29. O’Hanlon, S. J. et al. Recent Asian origin of chytrid fungi causing global amphibian declines. Science 360, 621–627 (2018).

    PubMed  PubMed Central  Google Scholar 

  30. Greenspan, S. E. et al. Hybrids of amphibian chytrid show high virulence in native hosts. Sci. Rep. 8, 9600 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Wallace, A. R. Darwinism: An Exposition of the Theory of Natural Selection, with Some of Its Applications (Cosimo Inc., 2007).

  32. Kuehne, H. A., Murphy, H. A., Francis, C. A. & Sniegowski, P. D. Allopatric divergence, secondary contact, and genetic isolation in wild yeast populations. Curr. Biol. 17, 407–411 (2007).

    CAS  PubMed  Google Scholar 

  33. Giraud, T. & Gourbière, S. The tempo and modes of evolution of reproductive isolation in fungi. Heredity 109, 204–214 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Turner, E., Jacobson, D. J. & Taylor, J. W. Reinforced postmating reproductive isolation barriers in Neurospora, an Ascomycete microfungus. J. Evol. Biol. 23, 1642–1656 (2010).

    CAS  PubMed  Google Scholar 

  35. Gac, M. L. E. & Giraud, T. Existence of a pattern of reproductive character displacement in Homobasidiomycota but not in Ascomycota. J. Evol. Biol. 21, 761–772 (2008).

    PubMed  Google Scholar 

  36. Brasier, C. The rise of the hybrid fungi. Nature 405, 134–135 (2000).

    CAS  PubMed  Google Scholar 

  37. Dujon, B. A. & Louis, E. J. Genome diversity and evolution in the budding yeasts (Saccharomycotina). Genetics 206, 717–750 (2017).

    PubMed  PubMed Central  Google Scholar 

  38. Dettman, J. R., Sirjusingh, C., Kohn, L. M. & Anderson, J. B. Incipient speciation by divergent adaptation and antagonistic epistasis in yeast. Nature 447, 585–588 (2007).

    CAS  PubMed  Google Scholar 

  39. Paoletti, M. Vegetative incompatibility in fungi: From recognition to cell death, whatever does the trick. Fungal Biol. Rev. 30, 152–162 (2016).

    Google Scholar 

  40. Rogers, D. W., McConnell, E., Ono, J. & Greig, D. Spore-autonomous fluorescent protein expression identifies meiotic chromosome mis-segregation as the principal cause of hybrid sterility in yeast. PLoS Biol. 16, e2005066 (2018).

    PubMed  PubMed Central  Google Scholar 

  41. Bozdag, G. O. et al. Engineering recombination between diverged yeast species reveals genetic incompatibilities. bioRxiv https://doi.org/10.1101/755165 (2019).

    Article  Google Scholar 

  42. Charron, G., Marsit, S., Hénault, M., Martin, H. & Landry, C. R. Spontaneous whole-genome duplication restores fertility in interspecific hybrids. Nat. Commun. 10, 4126 (2019).

    PubMed  PubMed Central  Google Scholar 

  43. Ortiz-Merino, R. A. et al. Evolutionary restoration of fertility in an interspecies hybrid yeast, by whole-genome duplication after a failed mating-type switch. PLoS Biol. 15, e2002128 (2017).

    PubMed  PubMed Central  Google Scholar 

  44. Wolfe, K. H. Origin of the yeast whole-genome duplication. PLoS Biol. 13, e1002221 (2015).

    PubMed  PubMed Central  Google Scholar 

  45. Marcet-Houben, M. & Gabaldón, T. Beyond the whole-genome duplication: Phylogenetic evidence for an ancient interspecies hybridization in the baker’s yeast lineage. PLoS Biol. 13, e1002220 (2015).

    PubMed  PubMed Central  Google Scholar 

  46. Mozzachiodi, S. et al. Aborting meiosis overcomes hybrid sterility. bioRxiv https://doi.org/10.1101/2020.12.04.411579 (2020).

    Article  Google Scholar 

  47. Leducq, J. B. et al. Speciation driven by hybridization and chromosomal plasticity in a wild yeast. Nat. Microbiol. 1, 1–10 (2016).

    Google Scholar 

  48. Stukenbrock, E. H., Christiansen, F. B., Hansen, T. T., Dutheil, J. Y. & Schierup, M. H. Fusion of two divergent fungal individuals led to the recent emergence of a unique widespread pathogen species. Proc. Natl Acad. Sci. USA 109, 10954–10959 (2012). This article describes one of the few cases of homoploid speciation discovered in fungi to date.

    CAS  PubMed  PubMed Central  Google Scholar 

  49. Bar-Zvi, D., Lupo, O., Levy, A. A. & Barkai, N. Hybrid vigor: the best of both parents, or a genomic clash? Curr. Opin. Syst. Biol. 6, 22–27 (2017).

    Google Scholar 

  50. Birchler, J. A., Yao, H., Chudalayandi, S., Vaiman, D. & Veitia, R. A. Heterosis. Plant Cell 22, 2105–2112 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  51. Carlborg, Ö. & Haley, C. S. Epistasis: too often neglected in complex trait studies? Nat. Rev. Genet. 5, 618–625 (2004).

    CAS  PubMed  Google Scholar 

  52. Krogerus, K. et al. Ploidy influences the functional attributes of de novo lager yeast hybrids. Appl. Microbiol. Biotechnol. 100, 7203–7222 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Herbst, R. H. et al. Heterosis as a consequence of regulatory incompatibility. BMC Biol. 15, 38 (2017).

    PubMed  PubMed Central  Google Scholar 

  54. Tirosh, I., Reikhav, S., Levy, A. A. & Barkai, N. A yeast hybrid provides insight into the evolution of gene expression regulation. Science 324, 659–662 (2009). In this article, the authors map the contribution of cis and trans polymorphisms to expression variation in an interspecific yeast hybrid.

    CAS  PubMed  Google Scholar 

  55. Feurtey, A., Stevens, D. M., Stephan, W. & Stukenbrock, E. H. Interspecific gene exchange introduces high genetic variability in crop pathogen. Genome Biol. Evol. 11, 3095–9105 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Corcoran, P. et al. Introgression maintains the genetic integrity of the mating-type determining chromosome of the fungus Neurospora tetrasperma. Genome Res. 26, 486–498 (2016). By investigating 92 Neurospora genomes, the authors identify many cases of adaptive introgressions in the mat locus.

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Sun, Y. et al. Large-scale introgression shapes the evolution of the mating-type chromosomes of the filamentous ascomycete Neurospora tetrasperma. PLoS Genet. 8, e1002820 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  58. Peter, J. et al. Genome evolution across 1,011 Saccharomyces cerevisiae isolates. Nature 556, 339–344 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  59. Langdon, Q. K. et al. Fermentation innovation through complex hybridization of wild and domesticated yeasts. Nat. Ecol. Evol. 3, 1576–1586 (2019).

    PubMed  PubMed Central  Google Scholar 

  60. Magwene, P. M. et al. Outcrossing, mitotic recombination, and life-history trade-offs shape genome evolution in Saccharomyces cerevisiae. Proc. Natl Acad. Sci. USA 108, 1987–1992 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Pryszcz, L. P. et al. The genomic aftermath of hybridization in the opportunistic pathogen Candida metapsilosis. PLOS Genet. 11, e1005626 (2015).

    PubMed  PubMed Central  Google Scholar 

  62. Vishnoi, A., Sethupathy, P., Simola, D., Plotkin, J. B. & Hannenhalli, S. Genome-wide survey of natural selection on functional, structural, and network properties of polymorphic sites in Saccharomyces paradoxus. Mol. Biol. Evol. 28, 2615–2627 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Taylor, S. A. & Larson, E. L. Insights from genomes into the evolutionary importance and prevalence of hybridization in nature. Nat. Ecol. Evol. 3, 170–177 (2019).

    PubMed  Google Scholar 

  64. Lancaster, S. M., Payen, C., Smukowski Heil, C. & Dunham, M. J. Fitness benefits of loss of heterozygosity in Saccharomyces hybrids. Genome Res. 29, 1685–1692 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Smukowski Heil, C. S. et al. Loss of heterozygosity drives adaptation in hybrid yeast. Mol. Biol. Evol. 34, 1596–1612 (2017). In this article, the authors demonstrate how LOH can be adaptive in experimentally evolved populations of hybrid yeast.

    PubMed  PubMed Central  Google Scholar 

  66. Zhang, Z. et al. Recombining your way out of trouble: the genetic architecture of hybrid fitness under environmental stress. Mol. Biol. Evol. 37, 167–182 (2020).

    CAS  PubMed  Google Scholar 

  67. Smukowski Heil, C. S. et al. Temperature preference can bias parental genome retention during hybrid evolution. PLoS Genet. 15, e1008383 (2019).

    PubMed  PubMed Central  Google Scholar 

  68. Mixão, V. & Gabaldón, T. Genomic evidence for a hybrid origin of the yeast opportunistic pathogen Candida albicans. BMC Biol. 18, 48 (2020).

    PubMed  PubMed Central  Google Scholar 

  69. Liang, S. H. & Bennett, R. J. The impact of gene dosage and heterozygosity on the diploid pathobiont Candida albicans. J. Fungi 6, 10 (2020).

    CAS  Google Scholar 

  70. Ford, C. B. et al. The evolution of drug resistance in clinical isolates of Candida albicans. eLife 2015, 1–27 (2015).

    Google Scholar 

  71. Selmecki, A. M. et al. Polyploidy can drive rapid adaptation in yeast. Nature 519, 349–352 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  72. Pavelka, N. et al. Aneuploidy confers quantitative proteome changes and phenotypic variation in budding yeast. Nature 468, 321–325 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  73. Yang, F. et al. Aneuploidy enables cross-adaptation to unrelated drugs. Mol. Biol. Evol. 36, 1768–1782 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Gilchrist, C. & Stelkens, R. Aneuploidy in yeast: segregation error or adaptation mechanism? Yeast 36, 525–539 (2019).

    CAS  Google Scholar 

  75. Yona, A. H. et al. Chromosomal duplication is a transient evolutionary solution to stress. Proc. Natl Acad. Sci. USA 109, 21010–21015 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  76. Hu, G. et al. Variation in chromosome copy number influences the virulence of Cryptococcus neoformans and occurs in isolates from AIDS patients. BMC Genomics 12, 526 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  77. van den Broek, M. et al. Chromosomal copy number variation in Saccharomyces pastorianus is evidence for extensive genome dynamics in industrial lager brewing strains. Appl. Environ. Microbiol. 81, 6253–6267 (2015).

    PubMed  PubMed Central  Google Scholar 

  78. Van De Peer, Y., Mizrachi, E. & Marchal, K. The evolutionary significance of polyploidy. Nat. Rev. Genet. 18, 411–424 (2017).

    PubMed  Google Scholar 

  79. Basse, C. W. Mitochondrial inheritance in fungi. Curr. Opin. Microbiol. 13, 712–719 (2010).

    CAS  PubMed  Google Scholar 

  80. Olson, Å. & Stenlid, J. Mitochondrial control of fungal hybrid virulence. Nature 411, 438 (2001).

    CAS  PubMed  Google Scholar 

  81. Giordano, L., Sillo, F., Garbelotto, M. & Gonthier, P. Mitonuclear interactions may contribute to fitness of fungal hybrids. Sci. Rep. 8, 1706 (2018).

    PubMed  PubMed Central  Google Scholar 

  82. Barr, C. M., Neiman, M. & Taylor, D. R. Inheritance and recombination of mitochondrial genomes in plants, fungi and animals. New Phytol. 168, 39–50 (2005).

    CAS  PubMed  Google Scholar 

  83. Chou, J. Y., Hung, Y. S., Lin, K. H., Lee, H. Y. & Leu, J. Y. Multiple molecular mechanisms cause reproductive isolation between three yeast species. PLoS Biol. 8, e1000432 (2010).

    PubMed  PubMed Central  Google Scholar 

  84. Lee, H.-Y. et al. Incompatibility of nuclear and mitochondrial genomes causes hybrid sterility between two yeast species. Cell 135, 1065–1073 (2008).

    CAS  PubMed  Google Scholar 

  85. Jhuang, H.-Y., Lee, H.-Y. & Leu, J.-Y. Mitochondrial-nuclear co-evolution leads to hybrid incompatibility through pentatricopeptide repeat proteins. EMBO Rep. 18, 87–101 (2017).

    CAS  PubMed  Google Scholar 

  86. Hou, J., Friedrich, A., Gounot, J. S. & Schacherer, J. Comprehensive survey of condition-specific reproductive isolation reveals genetic incompatibility in yeast. Nat. Commun. 6, 1–8 (2015).

    CAS  Google Scholar 

  87. Baker, E. et al. The genome sequence of Saccharomyces eubayanus and the domestication of lager-brewing yeasts. Mol. Biol. Evol. 32, 2818–2831 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  88. Mertens, S. et al. A large set of newly created interspecific Saccharomyces hybrids increases aromatic diversity in lager beers. Appl. Environ. Microbiol. 81, 8202–8214 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  89. Baker, E. C. P. et al. Mitochondrial DNA and temperature tolerance in lager yeasts. Sci. Adv. 5, eaav1869 (2019).

    PubMed  PubMed Central  Google Scholar 

  90. Li, X. C., Peris, D., Hittinger, C. T., Sia, E. A. & Fay, J. C. Mitochondria-encoded genes contribute to evolution of heat and cold tolerance in yeast. Sci. Adv. 5, eaav1848 (2019).

    PubMed  PubMed Central  Google Scholar 

  91. Grover, C. E. et al. Homoeolog expression bias and expression level dominance in allopolyploids. New Phytol. 196, 966–971 (2012).

    CAS  PubMed  Google Scholar 

  92. Yoo, M.-J., Liu, X., Pires, J. C., Soltis, P. S. & Soltis, D. E. Nonadditive gene expression in polyploids. Annu. Rev. Genet. 48, 485–517 (2014).

    CAS  PubMed  Google Scholar 

  93. Steige, K. A. & Slotte, T. Genomic legacies of the progenitors and the evolutionary consequences of allopolyploidy. Curr. Opin. Plant Biol. 30, 88–93 (2016).

    PubMed  Google Scholar 

  94. Bird, K. A., VanBuren, R., Puzey, J. R. & Edger, P. P. The causes and consequences of subgenome dominance in hybrids and recent polyploids. New Phytol. 220, 87–93 (2018).

    PubMed  Google Scholar 

  95. Edger, P. P. et al. Origin and evolution of the octoploid strawberry genome. Nat. Genet. 51, 541–547 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  96. De Smet, R. & Van de Peer, Y. Redundancy and rewiring of genetic networks following genome-wide duplication events. Curr. Opin. Plant Biol. 15, 168–176 (2012).

    PubMed  Google Scholar 

  97. Landry, C. R. et al. Compensatory cis-trans evolution and the dysregulation of gene expression in interspecific hybrids of Drosophila. Genetics 171, 1813–1822 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  98. Takahasi, K. R., Matsuo, T. & Takano-Shimizu-Kouno, T. Two types of cis-trans compensation in the evolution of transcriptional regulation. Proc. Natl Acad. Sci. USA 108, 15276–15281 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  99. Zhu, W. et al. Altered chromatin compaction and histone methylation drive non-additive gene expression in an interspecific Arabidopsis hybrid. Genome Biol. 18, 1–16 (2017).

    Google Scholar 

  100. Lopez-Maestre, H. et al. Identification of misexpressed genetic elements in hybrids between Drosophila-related species. Sci. Rep. 7, 1–13 (2017).

    Google Scholar 

  101. Wu, Y. et al. Transcriptome shock in an interspecific F1 triploid hybrid of Oryza revealed by RNA sequencing. J. Integr. Plant Biol. 58, 150–164 (2016).

    CAS  PubMed  Google Scholar 

  102. Cox, M. P. et al. An interspecific fungal hybrid reveals cross-kingdom rules for allopolyploid gene expression patterns. PLoS Genet. 10, e1004180 (2014). In this article, the authors describe how the transcriptional response to hybridization is conserved between fungi and plants, and how this reflects conservation of the mutational processes underlying eukaryotic gene regulatory evolution.

    PubMed  PubMed Central  Google Scholar 

  103. Olesen, K., Felding, T., Gjermansen, C. & Hansen, J. The dynamics of the Saccharomyces carlsbergensis brewing yeast transcriptome during a production-scale lager beer fermentation. FEMS Yeast Res. 2, 563–573 (2002).

    CAS  PubMed  Google Scholar 

  104. Horinouchi, T. et al. Genome-wide expression analysis of Saccharomyces pastorianus orthologous genes using oligonucleotide microarrays. J. Biosci. Bioeng. 110, 602–607 (2010).

    CAS  PubMed  Google Scholar 

  105. Hovhannisyan, H. et al. Integrative omics analysis reveals a limited transcriptional shock after yeast interspecies hybridization. Front. Genet. 11, 404 (2020).

    CAS  PubMed  PubMed Central  Google Scholar 

  106. Sriswasdi, S., Takashima, M., ichiroh Manabe, R., Ohkuma, M. & Iwasaki, W. Genome and transcriptome evolve separately in recently hybridized Trichosporon fungi. Commun. Biol. 2, 1–9 (2019).

    CAS  Google Scholar 

  107. Sriswasdi, S. et al. Global deceleration of gene evolution following recent genome hybridizations in fungi. Genome Res. 26, 1081–1090 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  108. Bolat, I., Romagnoli, G., Zhu, F., Pronk, J. T. & Daran, J. M. Functional analysis and transcriptional regulation of two orthologs of ARO10, encoding broad-substrate-specificity 2-oxo-acid decarboxylases, in the brewing yeast Saccharomyces pastorianus CBS1483. FEMS Yeast Res. 13, 505–517 (2013).

    CAS  PubMed  Google Scholar 

  109. Hovhannisyan, H., Saus, E., Ksiezopolska, E. & Gabaldón, T. The transcriptional aftermath in two independently formed hybrids of the opportunistic pathogen Candida orthopsilosis. mSphere 5, e00282-20 (2020).

    PubMed  PubMed Central  Google Scholar 

  110. Metzger, B. P. H., Wittkopp, P. J. & Coolon, J. D. Evolutionary dynamics of regulatory changes underlying gene expression divergence among Saccharomyces species. Genome Biol. Evol. 9, 843–854 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  111. Kellis, M., Patterson, N., Endrizzi, M., Birren, B. & Lander, E. S. Sequencing and comparison of yeast species to identify genes and regulatory elements. Nature 423, 241–254 (2003).

    CAS  PubMed  Google Scholar 

  112. Wu, J. et al. Homoeolog expression bias and expression level dominance in resynthesized allopolyploid Brassica napus. BMC Genomics 19, 586 (2018).

    PubMed  PubMed Central  Google Scholar 

  113. Yoo, M. J., Szadkowski, E. & Wendel, J. F. Homoeolog expression bias and expression level dominance in allopolyploid cotton. Heredity 110, 171–180 (2013).

    CAS  PubMed  Google Scholar 

  114. Campbell, M. A. et al. Epichloë hybrida, sp. nov., an emerging model system for investigating fungal allopolyploidy. Mycologia 109, 715–729 (2017).

    CAS  PubMed  Google Scholar 

  115. Krieger, G., Lupo, O., Levy, A. A. & Barkai, N. Independent evolution of transcript abundance and gene regulatory dynamics. Genome Res. 30, 1000–1011 (2020).

    CAS  PubMed  PubMed Central  Google Scholar 

  116. Tirosh, I. & Barkai, N. Inferring regulatory mechanisms from patterns of evolutionary divergence. Mol. Syst. Biol. 7, 530 (2011).

    PubMed  PubMed Central  Google Scholar 

  117. Metzger, B. P. H. et al. Contrasting frequencies and effects of cis- and trans-regulatory mutations affecting gene expression. Mol. Biol. Evol. 33, 1131–1146 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  118. Yang, B. & Wittkopp, P. J. Structure of the transcriptional regulatory network correlates with regulatory divergence in Drosophila. Mol. Biol. Evol. 34, 1352–1362 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  119. Li, X. C. & Fay, J. C. Cis-regulatory divergence in gene expression between two thermally divergent yeast species. Genome Biol. Evol. 9, 1120–1129 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  120. Christiaens, J. F. et al. Functional divergence of gene duplicates through ectopic recombination. EMBO Rep. 13, 1145–1151 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  121. Hewitt, S. K., Donaldson, I. J., Lovell, S. C. & Delneri, D. Sequencing and characterisation of rearrangements in three S. pastorianus strains reveals the presence of chimeric genes and gives evidence of breakpoint reuse. PLoS ONE 9, e92203 (2014).

    PubMed  PubMed Central  Google Scholar 

  122. Dunn, B. et al. Recurrent rearrangement during adaptive evolution in an interspecific yeast hybrid suggests a model for rapid introgression. PLoS Genet. 9, e1003366 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  123. Dandage, R. et al. Frequent assembly of chimeric complexes in the protein interaction network of an interspecies hybrid. Mol. Biol. Evol. https://doi.org/10.1093/molbev/msaa298 (2020).

    Article  PubMed Central  Google Scholar 

  124. Leducq, J.-B. et al. Evidence for the robustness of protein complexes to inter-species hybridization. PLoS Genet. 8, e1003161 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  125. Piatkowska, E. M., Naseeb, S., Knight, D. & Delneri, D. Chimeric protein complexes in hybrid species generate novel phenotypes. PLoS Genet. 9, e1003836 (2013).

    PubMed  PubMed Central  Google Scholar 

  126. Zamir, L. et al. Tight coevolution of proliferating cell nuclear antigen (PCNA)-partner interaction networks in fungi leads to interspecies network incompatibility. Proc. Natl Acad. Sci. USA 109, E406–E414 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  127. Hornsey, I. S. A History of Beer and Brewing (Royal Society of Chemistry, 2003).

  128. Steensels, J., Gallone, B., Voordeckers, K. & Verstrepen, K. J. Domestication of Industrial Microbes. Curr. Biol. 29, R381–R393 (2019).

    CAS  PubMed  Google Scholar 

  129. Gallone, B. et al. Origins, evolution, domestication and diversity of Saccharomyces beer yeasts. Curr. Opin. Biotechnol. 49, 148–155 (2018).

    CAS  PubMed  Google Scholar 

  130. Salazar, A. N. et al. Chromosome level assembly and comparative genome analysis confirm lager-brewing yeasts originated from a single hybridization. BMC Genomics 20, 916 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  131. Okuno, M. et al. Next-generation sequencing analysis of lager brewing yeast strains reveals the evolutionary history of interspecies hybridization. DNA Res. 23, dsv037 (2016).

    Google Scholar 

  132. Walther, A., Hesselbart, A. & Wendland, J. Genome sequence of Saccharomyces carlsbergensis, the world’s first pure culture lager yeast. G3 4, 783–793 (2014).

    PubMed  PubMed Central  Google Scholar 

  133. Monerawela, C., James, T. C., Wolfe, K. H. & Bond, U. Loss of lager specific genes and subtelomeric regions define two different Saccharomyces cerevisiae lineages for Saccharomyces pastorianus group I and II strains. FEMS Yeast Res. 15, fou008 (2015).

    PubMed  Google Scholar 

  134. Steensels, J. et al. Improving industrial yeast strains: exploiting natural and artificial diversity. FEMS Microbiol. Rev. 38, 947–995 (2014).

    CAS  PubMed  Google Scholar 

  135. Dzialo, M. C., Park, R., Steensels, J., Lievens, B. & Verstrepen, K. J. Physiology, ecology and industrial applications of aroma formation in yeast. FEMS Microbiol. Rev. 41, S95–S128 (2017).

    PubMed  PubMed Central  Google Scholar 

  136. Goold, H. D. et al. Yeast’s balancing act between ethanol and glycerol production in low-alcohol wines. Microb. Biotechnol. 10, 264–278 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  137. Bellon, J. R., Schmid, F., Capone, D. L., Dunn, B. L. & Chambers, P. J. Introducing a new breed of wine yeast: interspecific hybridisation between a commercial Saccharomyces cerevisiae wine yeast and Saccharomyces mikatae. PLoS ONE 8, e62053 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  138. Jetti, K. D., Gns, R. R., Garlapati, D. & Nammi, S. K. Improved ethanol productivity and ethanol tolerance through genome shuffling of Saccharomyces cerevisiae and Pichia stipitis. Int. Microbiol. 22, 247–254 (2019).

    CAS  PubMed  Google Scholar 

  139. Peris, D. et al. Synthetic hybrids of six yeast species. Nat. Commun. 11, 1–11 (2020).

    Google Scholar 

  140. Depotter, J. R. L., Seidl, M. F. & Wood, T. A. Interspecific hybridization impacts host range and pathogenicity of filamentous microbes. Curr. Opin. Microbiol. 32, 7–13 (2016).

    CAS  PubMed  Google Scholar 

  141. Brasier, C. M., Cooke, D. E. L. & Duncan, J. M. Origin of a new Phytophthora pathogen through interspecific hybridization. Proc. Natl Acad. Sci. USA 96, 5878–5883 (1999).

    CAS  PubMed  PubMed Central  Google Scholar 

  142. Hessenauer, P. et al. Hybridization and introgression drive genome evolution of Dutch elm disease pathogens. Nat. Ecol. Evol. 4, 626–638 (2020). This article describes how humans can facilitate hybridization between fungal species and in this way lead to new, highly virulent plant pathogens.

    PubMed  Google Scholar 

  143. Steenwyk, J. L. et al. Pathogenic allodiploid hybrids of Aspergillus fungi. Curr. Biol. 30, 2495–2507 (2020).

    CAS  PubMed  PubMed Central  Google Scholar 

  144. Pfaller, M. A. & Diekema, D. J. Epidemiology of invasive candidiasis: a persistent public health problem. Clin. Microbiol. Rev. 20, 133–163 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  145. Ropars, J. et al. Gene flow contributes to diversification of the major fungal pathogen Candida albicans. Nat. Commun. 9, 1–10 (2018).

    CAS  Google Scholar 

  146. Mixão, V. et al. Whole-genome sequencing of the opportunistic yeast pathogen Candida inconspicua uncovers its hybrid origin. Front. Genet. 10, 383 (2019).

    PubMed  PubMed Central  Google Scholar 

  147. Pryszcz, L. P., Németh, T., Gacser, A. & Gabaldón, T. Genome comparison of Candida Orthopsilosis clinical strains reveals the existence of hybrids between two distinct subspecies. Genome Biol. Evol. 6, 1069–1078 (2014).

    PubMed  PubMed Central  Google Scholar 

  148. Schröder, M. S. et al. Multiple origins of the pathogenic yeast Candida orthopsilosis by separate hybridizations between two parental species. PLoS Genet. 12, e1006404 (2016).

    PubMed  PubMed Central  Google Scholar 

  149. Glawe, D. A. The powdery mildews: a review of the world’s most familiar (yet poorly known) plant pathogens. Annu. Rev. Phytopathol. 46, 27–51 (2008).

    CAS  PubMed  Google Scholar 

  150. Wicker, T. et al. The wheat powdery mildew genome shows the unique evolution of an obligate biotroph. Nat. Genet. 45, 1092–1096 (2013).

    CAS  PubMed  Google Scholar 

  151. Menardo, F. et al. Hybridization of powdery mildew strains gives rise to pathogens on novel agricultural crop species. Nat. Genet. 48, 201–205 (2016).

    CAS  PubMed  Google Scholar 

  152. Walker, A. S., Bouguennec, A., Confais, J., Morgant, G. & Leroux, P. Evidence of host-range expansion from new powdery mildew (Blumeria graminis) infections of triticale (×Triticosecale) in France. Plant Pathol. 60, 207–220 (2011).

    CAS  Google Scholar 

  153. Troch, V., Audenaert, K., Bekaert, B., Höfte, M. & Haesaert, G. Phylogeography and virulence structure of the powdery mildew population on its ‘new’ host triticale. BMC Evol. Biol. 12, 76 (2012).

    PubMed  PubMed Central  Google Scholar 

  154. Shen, X. X. et al. Tempo and mode of genome evolution in the budding yeast subphylum. Cell 175, 1533–1545 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  155. Gallone, B. et al. Domestication and divergence of Saccharomyces cerevisiae beer yeasts. Cell 166, 1397–1410 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  156. Dujon, B. Yeasts illustrate the molecular mechanisms of eukaryotic genome evolution. Trends Genet. 22, 375–387 (2006).

    CAS  PubMed  Google Scholar 

  157. Gryganskyi, A. P. et al. Phylogenetic and phylogenomic definition of Rhizopus species. G3 8, 2007–2018 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  158. Wu, G. et al. Genus-wide comparative genomics of Malassezia delineates its phylogeny, physiology, and niche adaptation on human skin. PLoS Genet. 11, e1005614 (2015).

    PubMed  PubMed Central  Google Scholar 

  159. Bovers, M. et al. Unique hybrids between the fungal pathogens Cryptococcus neoformans and Cryptococcus gattii. FEMS Yeast Res. 6, 599–607 (2006).

    CAS  PubMed  Google Scholar 

  160. Libkind, D. et al. Microbe domestication and the identification of the wild genetic stock of lager-brewing yeast. Proc. Natl Acad. Sci. USA 108, 14539–14544 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  161. Peŕez-Través, L., Lopes, C. A., Querol, A. & Barrio, E. On the complexity of the Saccharomyces bayanus taxon: Hybridization and potential hybrid speciation. PLoS ONE 9, e93729 (2014).

    PubMed  PubMed Central  Google Scholar 

  162. Borneman, A. R., Zeppel, R., Chambers, P. J. & Curtin, C. D. Insights into the Dekkera bruxellensis genomic landscape: comparative genomics reveals variations in ploidy and nutrient utilisation potential amongst wine isolates. PLoS Genet. 10, e1004161 (2014).

    PubMed  PubMed Central  Google Scholar 

  163. Louis, V. L. et al. Pichia sorbitophila, an interspecies yeast hybrid, reveals early steps of genome resolution after polyploidization. G3 2, 299–311 (2012).

    PubMed  PubMed Central  Google Scholar 

  164. Saubin, M. et al. Investigation of genetic relationships between Hanseniaspora species found in grape musts revealed interspecific hybrids with dynamic genome structures. Front. Microbiol. 10, 2960 (2020).

    PubMed  PubMed Central  Google Scholar 

  165. Neafsey, D. E. et al. Population genomic sequencing of Coccidioides fungi reveals recent hybridization and transposon control. Genome Res. 20, 938–946 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  166. Staats, M., van Baarlen, P. & van Kan, J. A. L. Molecular phylogeny of the plant pathogenic genus Botrytis and the evolution of host specificity. Mol. Biol. Evol. 22, 333–346 (2004).

    PubMed  Google Scholar 

  167. Inderbitzin, P., Davis, R. M., Bostock, R. M. & Subbarao, K. V. The ascomycete Verticillium longisporum is a hybrid and a plant pathogen with an expanded host range. PLoS ONE 6, e18260 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  168. Nikulin, J., Krogerus, K. & Gibson, B. Alternative Saccharomyces interspecies hybrid combinations and their potential for low-temperature wort fermentation. Yeast 35, 113–127 (2018).

    CAS  PubMed  Google Scholar 

  169. Magalhães, F., Krogerus, K., Vidgren, V., Sandell, M. & Gibson, B. Improved cider fermentation performance and quality with newly generated Saccharomyces cerevisiae×Saccharomyces eubayanus hybrids. J. Ind. Microbiol. Biotechnol. 44, 1203–1213 (2017).

    PubMed  Google Scholar 

  170. Bizaj, E. et al. A breeding strategy to harness flavor diversity of Saccharomyces interspecific hybrids and minimize hydrogen sulfide production. FEMS Yeast Res. 12, 456–465 (2012).

    CAS  PubMed  Google Scholar 

  171. Peris, D. et al. Hybridization and adaptive evolution of diverse Saccharomyces species for cellulosic biofuel production. Biotechnol. Biofuels 10, 78 (2017).

    PubMed  PubMed Central  Google Scholar 

  172. Winans, M. J. et al. Saccharomyces arboricola and its hybrids’ propensity for sake production: interspecific hybrids reveal increased fermentation abilities and a mosaic metabolic profile. Fermentation 6, 14 (2020).

    CAS  Google Scholar 

  173. Varavallo, M. A. et al. Isolation of recombinant strains with enhanced pectinase production by protoplast fusion between Penicillium expansum and Penicillium griseoroseum. Brazilian J. Microbiol. 38, 52–57 (2007).

    Google Scholar 

  174. Kaur, B., Oberoi, H. S. & Chadha, B. S. Enhanced cellulase producing mutants developed from heterokaryotic Aspergillus strain. Bioresour. Technol. 156, 100–107 (2014).

    CAS  PubMed  Google Scholar 

  175. Guo, X., Wang, R., Chen, Y. & Xiao, D. Intergeneric yeast fusants with efficient ethanol production from cheese whey powder solution: construction of a Kluyveromyces marxianus and Saccharomyces cerevisiae AY-5 hybrid. Eng. Life Sci. 12, 656–661 (2012).

    CAS  Google Scholar 

  176. Ye, M., Yue, T., Yuan, Y. & Wang, L. Production of yeast hybrids for improvement of cider by protoplast electrofusion. Biochem. Eng. J. 81, 162–169 (2013).

    CAS  Google Scholar 

  177. Patil, N. S., Patil, S. M., Govindwar, S. P. & Jadhav, J. P. Molecular characterization of intergeneric hybrid between Aspergillus oryzae and Trichoderma harzianum by protoplast fusion. J. Appl. Microbiol. 118, 390–398 (2015).

    CAS  PubMed  Google Scholar 

  178. Deng, Z. et al. Enhanced phytoremediation of multi-metal contaminated soils by interspecific fusion between the protoplasts of endophytic Mucor sp. CBRF59 and Fusarium sp. CBRF14. Soil. Biol. Biochem. 77, 31–40 (2014).

    CAS  Google Scholar 

  179. Li, Y. et al. A genome-scale phylogeny of fungi; insights into early evolution, radiations, and the relationship between taxonomy and phylogeny. Curr. Biol. https://doi.org/10.1016/j.cub.2021.01.074 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  180. Leducq, J.-B. et al. Mitochondrial recombination and introgression during speciation by hybridization. Mol. Biol. Evol. 34, 1947–1959 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

K.J.V. acknowledges funding from KU Leuven, European Research Council (ERC) Consolidator Grant CoG682009, Vlaams Instituut voor Biotechnologie (VIB), Fonds voor Wetenschappelijk Onderzoek – Vlaanderen (FWO) and Vlaanderen Agentschap Innoveren & Ondernemen (VLAIO). J.S. acknowledges funding from FWO (grant number 12W3918N).

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Glossary

Interspecific hybridization

Defined in this Review as hybridization between two or more genetically isolated populations that can usually be generalized as ‘species’.

Heteroploid

The presence of an abnormal chromosome number in a cell, resulting from either aneuploidy or euploidy.

Gene flow

Transfer of genetic material from one population to another.

Selfing

Mating between gametes from the same diploid organism.

Conspecific

From the same species.

Heterospecific

From a different species.

Sympatric

Occurring in the same geographical location.

Allopatric

Occurring in a non-overlapping geographical location.

Aneuploid

Under-representation or over-representation of one or more chromosomes in a cell.

Euploidy

Chromosomal variation involving the entire set of chromosomes in a cell; for example, polyploidy, the presence of multiple copies of the entire set of chromosomes.

Flocculation

A reversible, asexual, calcium-dependent process in which cells adhere to form flocs consisting of thousands of cells.

Homoeologue expression bias

Unequal contribution of one homoeologue to the total gene expression.

Subgenome dominance

Genome-wide expression skewed towards one subgenome.

Homoeologous genes

Corresponding parent orthologues in the hybrid.

Orthologous genes

Homologous genes (those deriving from the same ancestral sequence) that arise from speciation.

Cis-regulatory elements

Non-coding regions, such as promoters, transcription factor-binding sites and terminators, which are near genes and are thus linked to a single subgenome.

Trans-regulatory elements

Elements such as transcription factors, chromatin regulators and signalling molecules which interact with cis elements but act independently of their own genomic location and are therefore shared by subgenomes residing in the same nucleus.

Subgenome homogenization

A process in which subgenomes in a hybrid become more uniform due to genome stabilization, such as by gene conversion.

Chimeric genes

Genes consisting of a fusion of the 5′ part of one parent gene to the 3′ end of the other parent gene.

Synteny

Co-occurrence of loci on the same chromosome among two species, with or without a conserved order.

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Steensels, J., Gallone, B. & Verstrepen, K.J. Interspecific hybridization as a driver of fungal evolution and adaptation. Nat Rev Microbiol 19, 485–500 (2021). https://doi.org/10.1038/s41579-021-00537-4

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