The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.

Candida metapsilosis is a rarely-isolated, opportunistic pathogen that belongs to a clade of pathogenic yeasts known as the C. parapsilosis sensu lato species complex. To gain insight into the recent evolution of C. metapsilosis and the genetic basis of its virulence, we sequenced the genome of 11 c...

Full description

Bibliographic Details
Main Authors: Leszek P Pryszcz, Tibor Németh, Ester Saus, Ewa Ksiezopolska, Eva Hegedűsová, Jozef Nosek, Kenneth H Wolfe, Attila Gacser, Toni Gabaldón
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-10-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4627764?pdf=render
_version_ 1818571317161492480
author Leszek P Pryszcz
Tibor Németh
Ester Saus
Ewa Ksiezopolska
Eva Hegedűsová
Jozef Nosek
Kenneth H Wolfe
Attila Gacser
Toni Gabaldón
author_facet Leszek P Pryszcz
Tibor Németh
Ester Saus
Ewa Ksiezopolska
Eva Hegedűsová
Jozef Nosek
Kenneth H Wolfe
Attila Gacser
Toni Gabaldón
author_sort Leszek P Pryszcz
collection DOAJ
description Candida metapsilosis is a rarely-isolated, opportunistic pathogen that belongs to a clade of pathogenic yeasts known as the C. parapsilosis sensu lato species complex. To gain insight into the recent evolution of C. metapsilosis and the genetic basis of its virulence, we sequenced the genome of 11 clinical isolates from various locations, which we compared to each other and to the available genomes of the two remaining members of the complex: C. orthopsilosis and C. parapsilosis. Unexpectedly, we found compelling genomic evidence that C. metapsilosis is a highly heterozygous hybrid species, with all sequenced clinical strains resulting from the same past hybridization event involving two parental lineages that were approximately 4.5% divergent in sequence. This result indicates that the parental species are non-pathogenic, but that hybridization between them formed a new opportunistic pathogen, C. metapsilosis, that has achieved a worldwide distribution. We show that these hybrids are diploid and we identified strains carrying loci for both alternative mating types, which supports mating as the initial mechanism for hybrid formation. We trace the aftermath of this hybridization at the genomic level, and reconstruct the evolutionary relationships among the different strains. Recombination and introgression -resulting in loss of heterozygosis- between the two subgenomes have been rampant, and includes the partial overwriting of the MTLa mating locus in all strains. Collectively, our results shed light on the recent genomic evolution within the C. parapsilosis sensu lato complex, and argue for a re-definition of species within this clade, with at least five distinct homozygous lineages, some of which having the ability to form hybrids.
first_indexed 2024-12-14T13:54:07Z
format Article
id doaj.art-0d84b75df2f54ee0b635b3a3fb810514
institution Directory Open Access Journal
issn 1553-7390
1553-7404
language English
last_indexed 2024-12-14T13:54:07Z
publishDate 2015-10-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj.art-0d84b75df2f54ee0b635b3a3fb8105142022-12-21T22:58:53ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-10-011110e100562610.1371/journal.pgen.1005626The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.Leszek P PryszczTibor NémethEster SausEwa KsiezopolskaEva HegedűsováJozef NosekKenneth H WolfeAttila GacserToni GabaldónCandida metapsilosis is a rarely-isolated, opportunistic pathogen that belongs to a clade of pathogenic yeasts known as the C. parapsilosis sensu lato species complex. To gain insight into the recent evolution of C. metapsilosis and the genetic basis of its virulence, we sequenced the genome of 11 clinical isolates from various locations, which we compared to each other and to the available genomes of the two remaining members of the complex: C. orthopsilosis and C. parapsilosis. Unexpectedly, we found compelling genomic evidence that C. metapsilosis is a highly heterozygous hybrid species, with all sequenced clinical strains resulting from the same past hybridization event involving two parental lineages that were approximately 4.5% divergent in sequence. This result indicates that the parental species are non-pathogenic, but that hybridization between them formed a new opportunistic pathogen, C. metapsilosis, that has achieved a worldwide distribution. We show that these hybrids are diploid and we identified strains carrying loci for both alternative mating types, which supports mating as the initial mechanism for hybrid formation. We trace the aftermath of this hybridization at the genomic level, and reconstruct the evolutionary relationships among the different strains. Recombination and introgression -resulting in loss of heterozygosis- between the two subgenomes have been rampant, and includes the partial overwriting of the MTLa mating locus in all strains. Collectively, our results shed light on the recent genomic evolution within the C. parapsilosis sensu lato complex, and argue for a re-definition of species within this clade, with at least five distinct homozygous lineages, some of which having the ability to form hybrids.http://europepmc.org/articles/PMC4627764?pdf=render
spellingShingle Leszek P Pryszcz
Tibor Németh
Ester Saus
Ewa Ksiezopolska
Eva Hegedűsová
Jozef Nosek
Kenneth H Wolfe
Attila Gacser
Toni Gabaldón
The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
PLoS Genetics
title The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
title_full The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
title_fullStr The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
title_full_unstemmed The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
title_short The Genomic Aftermath of Hybridization in the Opportunistic Pathogen Candida metapsilosis.
title_sort genomic aftermath of hybridization in the opportunistic pathogen candida metapsilosis
url http://europepmc.org/articles/PMC4627764?pdf=render
work_keys_str_mv AT leszekppryszcz thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT tibornemeth thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT estersaus thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT ewaksiezopolska thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT evahegedusova thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT jozefnosek thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT kennethhwolfe thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT attilagacser thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT tonigabaldon thegenomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT leszekppryszcz genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT tibornemeth genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT estersaus genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT ewaksiezopolska genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT evahegedusova genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT jozefnosek genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT kennethhwolfe genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT attilagacser genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis
AT tonigabaldon genomicaftermathofhybridizationintheopportunisticpathogencandidametapsilosis