Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.

Candida parapsilosis is a pathogenic fungus that is major cause of hospital-acquired infection, predominantly due to growth as biofilms on indwelling medical devices. It is related to Candida albicans, which remains the most common cause of candidiasis disease in humans. The transcription factor Bcr...

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Main Authors: Chen Ding, Genevieve M Vidanes, Sarah L Maguire, Alessandro Guida, John M Synnott, David R Andes, Geraldine Butler
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22145027/pdf/?tool=EBI
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author Chen Ding
Genevieve M Vidanes
Sarah L Maguire
Alessandro Guida
John M Synnott
David R Andes
Geraldine Butler
author_facet Chen Ding
Genevieve M Vidanes
Sarah L Maguire
Alessandro Guida
John M Synnott
David R Andes
Geraldine Butler
author_sort Chen Ding
collection DOAJ
description Candida parapsilosis is a pathogenic fungus that is major cause of hospital-acquired infection, predominantly due to growth as biofilms on indwelling medical devices. It is related to Candida albicans, which remains the most common cause of candidiasis disease in humans. The transcription factor Bcr1 is an important regulator of biofilm formation in vitro in both C. parapsilosis and C. albicans. We show here that C. parapsilosis Bcr1 is required for in vivo biofilm development in a rat catheter model, like C. albicans. By comparing the transcription profiles of a bcr1 deletion in both species we found that regulation of expression of the CFEM family is conserved. In C. albicans, three of the five CFEM cell wall proteins (Rbt5, Pga7 and Csa1) are associated with both biofilm formation and acquisition of iron from heme, which is an important virulence characteristic. In C. parapsilosis, the CFEM family has undergone an expansion to 7 members. Expression of three genes (CFEM2, CFEM3, and CFEM6) is dependent on Bcr1, and is induced in low iron conditions. All three are involved in the acquisition of iron from heme. However, deletion of the three CFEM genes has no effect on biofilm formation in C. parapsilosis. Our data suggest that the role of the CFEM family in iron acquisition is conserved between C. albicans and C. parapsilosis, but their role in biofilm formation is not.
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spelling doaj.art-3f2e593a1db246a281b806796846c9532022-12-21T20:30:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01612e2815110.1371/journal.pone.0028151Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.Chen DingGenevieve M VidanesSarah L MaguireAlessandro GuidaJohn M SynnottDavid R AndesGeraldine ButlerCandida parapsilosis is a pathogenic fungus that is major cause of hospital-acquired infection, predominantly due to growth as biofilms on indwelling medical devices. It is related to Candida albicans, which remains the most common cause of candidiasis disease in humans. The transcription factor Bcr1 is an important regulator of biofilm formation in vitro in both C. parapsilosis and C. albicans. We show here that C. parapsilosis Bcr1 is required for in vivo biofilm development in a rat catheter model, like C. albicans. By comparing the transcription profiles of a bcr1 deletion in both species we found that regulation of expression of the CFEM family is conserved. In C. albicans, three of the five CFEM cell wall proteins (Rbt5, Pga7 and Csa1) are associated with both biofilm formation and acquisition of iron from heme, which is an important virulence characteristic. In C. parapsilosis, the CFEM family has undergone an expansion to 7 members. Expression of three genes (CFEM2, CFEM3, and CFEM6) is dependent on Bcr1, and is induced in low iron conditions. All three are involved in the acquisition of iron from heme. However, deletion of the three CFEM genes has no effect on biofilm formation in C. parapsilosis. Our data suggest that the role of the CFEM family in iron acquisition is conserved between C. albicans and C. parapsilosis, but their role in biofilm formation is not.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22145027/pdf/?tool=EBI
spellingShingle Chen Ding
Genevieve M Vidanes
Sarah L Maguire
Alessandro Guida
John M Synnott
David R Andes
Geraldine Butler
Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
PLoS ONE
title Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
title_full Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
title_fullStr Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
title_full_unstemmed Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
title_short Conserved and divergent roles of Bcr1 and CFEM proteins in Candida parapsilosis and Candida albicans.
title_sort conserved and divergent roles of bcr1 and cfem proteins in candida parapsilosis and candida albicans
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22145027/pdf/?tool=EBI
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