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Comparative genomics of emerging pathogens in the Candida glabrata clade

BACKGROUND: Candida glabrata follows C. albicans as the second or third most prevalent cause of candidemia worldwide. These two pathogenic yeasts are distantly related, C. glabrata being part of the Nakaseomyces, a group more closely related to Saccharomyces cerevisiae. Although C. glabrata was thou...

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Autores principales: Gabaldón, Toni, Martin, Tiphaine, Marcet-Houben, Marina, Durrens, Pascal, Bolotin-Fukuhara, Monique, Lespinet, Olivier, Arnaise, Sylvie, Boisnard, Stéphanie, Aguileta, Gabriela, Atanasova, Ralitsa, Bouchier, Christiane, Couloux, Arnaud, Creno, Sophie, Almeida Cruz, Jose, Devillers, Hugo, Enache-Angoulvant, Adela, Guitard, Juliette, Jaouen, Laure, Ma, Laurence, Marck, Christian, Neuvéglise, Cécile, Pelletier, Eric, Pinard, Amélie, Poulain, Julie, Recoquillay, Julien, Westhof, Eric, Wincker, Patrick, Dujon, Bernard, Hennequin, Christophe, Fairhead, Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847288/
https://www.ncbi.nlm.nih.gov/pubmed/24034898
http://dx.doi.org/10.1186/1471-2164-14-623
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author Gabaldón, Toni
Martin, Tiphaine
Marcet-Houben, Marina
Durrens, Pascal
Bolotin-Fukuhara, Monique
Lespinet, Olivier
Arnaise, Sylvie
Boisnard, Stéphanie
Aguileta, Gabriela
Atanasova, Ralitsa
Bouchier, Christiane
Couloux, Arnaud
Creno, Sophie
Almeida Cruz, Jose
Devillers, Hugo
Enache-Angoulvant, Adela
Guitard, Juliette
Jaouen, Laure
Ma, Laurence
Marck, Christian
Neuvéglise, Cécile
Pelletier, Eric
Pinard, Amélie
Poulain, Julie
Recoquillay, Julien
Westhof, Eric
Wincker, Patrick
Dujon, Bernard
Hennequin, Christophe
Fairhead, Cécile
author_facet Gabaldón, Toni
Martin, Tiphaine
Marcet-Houben, Marina
Durrens, Pascal
Bolotin-Fukuhara, Monique
Lespinet, Olivier
Arnaise, Sylvie
Boisnard, Stéphanie
Aguileta, Gabriela
Atanasova, Ralitsa
Bouchier, Christiane
Couloux, Arnaud
Creno, Sophie
Almeida Cruz, Jose
Devillers, Hugo
Enache-Angoulvant, Adela
Guitard, Juliette
Jaouen, Laure
Ma, Laurence
Marck, Christian
Neuvéglise, Cécile
Pelletier, Eric
Pinard, Amélie
Poulain, Julie
Recoquillay, Julien
Westhof, Eric
Wincker, Patrick
Dujon, Bernard
Hennequin, Christophe
Fairhead, Cécile
author_sort Gabaldón, Toni
collection PubMed
description BACKGROUND: Candida glabrata follows C. albicans as the second or third most prevalent cause of candidemia worldwide. These two pathogenic yeasts are distantly related, C. glabrata being part of the Nakaseomyces, a group more closely related to Saccharomyces cerevisiae. Although C. glabrata was thought to be the only pathogenic Nakaseomyces, two new pathogens have recently been described within this group: C. nivariensis and C. bracarensis. To gain insight into the genomic changes underlying the emergence of virulence, we sequenced the genomes of these two, and three other non-pathogenic Nakaseomyces, and compared them to other sequenced yeasts. RESULTS: Our results indicate that the two new pathogens are more closely related to the non-pathogenic N. delphensis than to C. glabrata. We uncover duplications and accelerated evolution that specifically affected genes in the lineage preceding the group containing N. delphensis and the three pathogens, which may provide clues to the higher propensity of this group to infect humans. Finally, the number of Epa-like adhesins is specifically enriched in the pathogens, particularly in C. glabrata. CONCLUSIONS: Remarkably, some features thought to be the result of adaptation of C. glabrata to a pathogenic lifestyle, are present throughout the Nakaseomyces, indicating these are rather ancient adaptations to other environments. Phylogeny suggests that human pathogenesis evolved several times, independently within the clade. The expansion of the EPA gene family in pathogens establishes an evolutionary link between adhesion and virulence phenotypes. Our analyses thus shed light onto the relationships between virulence and the recent genomic changes that occurred within the Nakaseomyces. SEQUENCE ACCESSION NUMBERS: Nakaseomyces delphensis: CAPT01000001 to CAPT01000179 Candida bracarensis: CAPU01000001 to CAPU01000251 Candida nivariensis: CAPV01000001 to CAPV01000123 Candida castellii: CAPW01000001 to CAPW01000101 Nakaseomyces bacillisporus: CAPX01000001 to CAPX01000186
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spelling pubmed-38472882013-12-04 Comparative genomics of emerging pathogens in the Candida glabrata clade Gabaldón, Toni Martin, Tiphaine Marcet-Houben, Marina Durrens, Pascal Bolotin-Fukuhara, Monique Lespinet, Olivier Arnaise, Sylvie Boisnard, Stéphanie Aguileta, Gabriela Atanasova, Ralitsa Bouchier, Christiane Couloux, Arnaud Creno, Sophie Almeida Cruz, Jose Devillers, Hugo Enache-Angoulvant, Adela Guitard, Juliette Jaouen, Laure Ma, Laurence Marck, Christian Neuvéglise, Cécile Pelletier, Eric Pinard, Amélie Poulain, Julie Recoquillay, Julien Westhof, Eric Wincker, Patrick Dujon, Bernard Hennequin, Christophe Fairhead, Cécile BMC Genomics Research Article BACKGROUND: Candida glabrata follows C. albicans as the second or third most prevalent cause of candidemia worldwide. These two pathogenic yeasts are distantly related, C. glabrata being part of the Nakaseomyces, a group more closely related to Saccharomyces cerevisiae. Although C. glabrata was thought to be the only pathogenic Nakaseomyces, two new pathogens have recently been described within this group: C. nivariensis and C. bracarensis. To gain insight into the genomic changes underlying the emergence of virulence, we sequenced the genomes of these two, and three other non-pathogenic Nakaseomyces, and compared them to other sequenced yeasts. RESULTS: Our results indicate that the two new pathogens are more closely related to the non-pathogenic N. delphensis than to C. glabrata. We uncover duplications and accelerated evolution that specifically affected genes in the lineage preceding the group containing N. delphensis and the three pathogens, which may provide clues to the higher propensity of this group to infect humans. Finally, the number of Epa-like adhesins is specifically enriched in the pathogens, particularly in C. glabrata. CONCLUSIONS: Remarkably, some features thought to be the result of adaptation of C. glabrata to a pathogenic lifestyle, are present throughout the Nakaseomyces, indicating these are rather ancient adaptations to other environments. Phylogeny suggests that human pathogenesis evolved several times, independently within the clade. The expansion of the EPA gene family in pathogens establishes an evolutionary link between adhesion and virulence phenotypes. Our analyses thus shed light onto the relationships between virulence and the recent genomic changes that occurred within the Nakaseomyces. SEQUENCE ACCESSION NUMBERS: Nakaseomyces delphensis: CAPT01000001 to CAPT01000179 Candida bracarensis: CAPU01000001 to CAPU01000251 Candida nivariensis: CAPV01000001 to CAPV01000123 Candida castellii: CAPW01000001 to CAPW01000101 Nakaseomyces bacillisporus: CAPX01000001 to CAPX01000186 BioMed Central 2013-09-14 /pmc/articles/PMC3847288/ /pubmed/24034898 http://dx.doi.org/10.1186/1471-2164-14-623 Text en Copyright © 2013 Gabaldón et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gabaldón, Toni
Martin, Tiphaine
Marcet-Houben, Marina
Durrens, Pascal
Bolotin-Fukuhara, Monique
Lespinet, Olivier
Arnaise, Sylvie
Boisnard, Stéphanie
Aguileta, Gabriela
Atanasova, Ralitsa
Bouchier, Christiane
Couloux, Arnaud
Creno, Sophie
Almeida Cruz, Jose
Devillers, Hugo
Enache-Angoulvant, Adela
Guitard, Juliette
Jaouen, Laure
Ma, Laurence
Marck, Christian
Neuvéglise, Cécile
Pelletier, Eric
Pinard, Amélie
Poulain, Julie
Recoquillay, Julien
Westhof, Eric
Wincker, Patrick
Dujon, Bernard
Hennequin, Christophe
Fairhead, Cécile
Comparative genomics of emerging pathogens in the Candida glabrata clade
title Comparative genomics of emerging pathogens in the Candida glabrata clade
title_full Comparative genomics of emerging pathogens in the Candida glabrata clade
title_fullStr Comparative genomics of emerging pathogens in the Candida glabrata clade
title_full_unstemmed Comparative genomics of emerging pathogens in the Candida glabrata clade
title_short Comparative genomics of emerging pathogens in the Candida glabrata clade
title_sort comparative genomics of emerging pathogens in the candida glabrata clade
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847288/
https://www.ncbi.nlm.nih.gov/pubmed/24034898
http://dx.doi.org/10.1186/1471-2164-14-623
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