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PMID: 27806045 Published · epublish English Journal Article

Multiple Origins of the Pathogenic Yeast Candida orthopsilosis by Separate Hybridizations between Two Parental Species.

PLoS genetics ·Vol. 12 ·No. 11 ·2016-11-00 ·Pages e1006404

Schröder MS, Martinez de San Vicente K, Prandini TH, Hammel S, Higgins DG, Bagagli E, Wolfe KH, Butler G

Abstract

Mating between different species produces hybrids that are usually asexual and stuck as diploids, but can also lead to the formation of new species. Here, we report the genome sequences of 27 isolates of the pathogenic yeast Candida orthopsilosis. We find that most isolates are diploid hybrids, products of mating between two unknown parental species (A and B) that are 5% divergent in sequence. Isolates vary greatly in the extent of homogenization between A and B, making their genomes a mosaic of highly heterozygous regions interspersed with homozygous regions. Separate phylogenetic analyses of SNPs in the A- and B-derived portions of the genome produces almost identical trees of the isolates with four major clades. However, the presence of two mutually exclusive genotype combinations at the mating type locus, and recombinant mitochondrial genomes diagnostic of inter-clade mating, shows that the species C. orthopsilosis does not have a single evolutionary origin but was created at least four times by separate interspecies hybridizations between parents A and B. Older hybrids have lost more heterozygosity. We also identify two isolates with homozygous genomes derived exclusively from parent A, which are pure non-hybrid strains. The parallel emergence of the same hybrid species from multiple independent hybridization events is common in plant evolution, but is much less documented in pathogenic fungi.

MeSH Terms
Animals Candida/genetics,growth & development Diploidy Genetic Speciation Genome, Fungal Haplotypes Heterozygote Hybridization, Genetic Larva/genetics Mitochondria/genetics Phylogeny Polymorphism, Single Nucleotide Saccharomyces cerevisiae/genetics
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Schröder Markus S ORCID
School of Biomedical and Biomolecular Science and UCD Conway Institute of Biomolecular and Biomedical Research, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Martinez de San Vicente Kontxi ORCID
School of Biomedical and Biomolecular Science and UCD Conway Institute of Biomolecular and Biomedical Research, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Prandini Tâmara H R ORCID
Instituto de Biociências, UNESP - Univ Estadual Paulista, Botucatu, Sao Paulo, Brazil.
Hammel Stephen
School of Biomedical and Biomolecular Science and UCD Conway Institute of Biomolecular and Biomedical Research, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Higgins Desmond G
School of Medicine and UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, Ireland.
Bagagli Eduardo
Instituto de Biociências, UNESP - Univ Estadual Paulista, Botucatu, Sao Paulo, Brazil.
Wolfe Kenneth H ORCID
School of Medicine and UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, Ireland.
Butler Geraldine ORCID
School of Biomedical and Biomolecular Science and UCD Conway Institute of Biomolecular and Biomedical Research, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
Conflict of Interest

The authors have declared that no competing interests exist.

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Article Info
Journal
PLoS genetics
Abbr.
PLoS Genet
ISSN
1553-7404
Published
2016-11-00
Epub
2016-00-02
Pages
e1006404
Language
English
Region
United States
NLM ID
101239074
PMCID
PMC5091853
Subset
IM
Grants
Wellcome Trust · United Kingdom
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