A high-resolution haplotype collection uncovers somatic hybridization, recombination and intercontinental movement in oat crown rust
The population structure and evolution of basidiomycetes like rust fungi are influenced by complex reproductive cycles and dikaryotic life stages where two independent nuclear haplotypes are present in the cell. The ability to alternate between asexual (clonal) and sexual reproduction increases the evolutionary capacity in these species. Furthermore, exchange of intact nuclei (somatic hybridization) in rust fungi can allow for rapid generation of genetic variability outside of the sexual cycle. Puccinia coronata f. sp. avenae (Pca), the causal agent of oat crown rust, is a pathogen of global economic importance that is difficult to control due to rapid breakdown of host genetic resistance. The contribution of sexuality, clonality, and migration to virulence evolution varies across Pca populations. As such, the Pca pathosystem is ideal to address the role of mating type, recombination, mutation, and somatic hybridization in host adaptation. We expanded the existing resources for USA and South African populations by generating whole genome sequencing data of Taiwanese and Australian isolates. An atlas of 30 chromosome-level, fully-phased nuclear haplotypes from six USA isolates and nine Australian isolates was created to capture the genomic composition of key Pca lineages. At the haplotype level, we confirmed previous reports of genetic recombination in the USA population and additionally detected either sexual or cryptic recombination between Australian isolates, contrasting previous evaluations that suggested Pca populations in Australia to be purely clonal. We also identified somatic hybridization events in Pca that are not only associated with significant changes in fitness but also imply intercontinental migration of haplotypes, which provides further impetus for molecular monitoring of rust pathogen populations on a global scale.
Authors
- Yung‐Fen Huang (ORCID: https://orcid.org/0000-0001-7854-2764)
- Eric S. Nazareno (ORCID: https://orcid.org/0000-0001-5192-2644)
- Kyle W. Langford (ORCID: https://orcid.org/0009-0008-9226-7218)
- Hayley Mangelson (ORCID: https://orcid.org/0000-0002-1520-9099)
- Ivan Liachko (ORCID: https://orcid.org/0000-0001-6972-6705)
- Shahryar F. Kianian (ORCID: https://orcid.org/0000-0003-4968-3140)
- Eva C. Henningsen (ORCID: https://orcid.org/0000-0001-9619-3705)
- Melania Figueroa (ORCID: https://orcid.org/0000-0003-2636-661X)
- Jana Sperschneider (ORCID: https://orcid.org/0000-0002-9385-8588)
- Peter N. Dodds (ORCID: https://orcid.org/0000-0003-0620-5923)
- Brian J. Steffenson (ORCID: https://orcid.org/0000-0001-7961-5363)
- Brendan Boesen
- Eric Stone (ORCID: https://orcid.org/0000-0002-2725-4209)
- David C. Lewis (ORCID: https://orcid.org/0000-0002-9374-6332)
Institutions
- Australian National University (AU)
- Commonwealth Scientific and Industrial Research Organisation (AU)
- University of Minnesota (US)
- National Taiwan University (TW)
- ID Genomics (United States) (US)
- Cereal Disease Laboratory (US)
- ACT Government (AU)
Publication Details
- Journal
- PLoS Genetics
- Published
- 2024-11-21
- DOI
- https://doi.org/10.1371/journal.pgen.1011493
- Citations
- 18
- Primary Topic
- Yeasts and Rust Fungi Studies
- Type
- article
- Field-Weighted Citation Impact
- 4.21
Funders
- U.S. Department of Agriculture
- Australian Government
- Commonwealth Scientific and Industrial Research Organisation
- Grains Research and Development Corporation
- National Science and Technology Council
- National Institute of Food and Agriculture
- Agricultural Research Service
- Biotechnology and Biological Sciences Research Council