A Recently Evolved Transcriptional Network Controls Biofilm Development in Candida albicans
A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast...
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| Published in | Cell Vol. 148; no. 1-2; pp. 126 - 138 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Inc
20.01.2012
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0092-8674 1097-4172 1097-4172 |
| DOI | 10.1016/j.cell.2011.10.048 |
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| Abstract | A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits.
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► Candida biofilms are controlled by a network of six master transcription regulators ► The biofilm network is highly interconnected and contains > 1,000 target genes ► Computational analysis indicates that the biofilm network has rapidly evolved ► The network interconnectedness provides clues as to how complex circuits evolve
Biofilms of the pathogenic fungus C. albicans coat medical devices and contribute to drug-resistant infections. Revealing the transcriptional circuit responsible for biofilm formation provides insight into how complex cell behaviors arise from the evolution of regulatory circuits. |
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| AbstractList | A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits.A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. [Display omitted] ► Candida biofilms are controlled by a network of six master transcription regulators ► The biofilm network is highly interconnected and contains > 1,000 target genes ► Computational analysis indicates that the biofilm network has rapidly evolved ► The network interconnectedness provides clues as to how complex circuits evolve Biofilms of the pathogenic fungus C. albicans coat medical devices and contribute to drug-resistant infections. Revealing the transcriptional circuit responsible for biofilm formation provides insight into how complex cell behaviors arise from the evolution of regulatory circuits. A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with similar to 1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. A biofilm is an organized, resilient group of microbes where individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans , whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ~1000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted towards genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those observed in suspension cultures. Here, we describe and analyze the transcriptional network controlling biofilm formation in the pathogenic yeast Candida albicans, whose biofilms are a major source of medical device-associated infections. We have combined genetic screens, genome-wide approaches, and two in vivo animal models to describe a master circuit controlling biofilm formation, composed of six transcription regulators that form a tightly woven network with ∼1,000 target genes. Evolutionary analysis indicates that the biofilm network has rapidly evolved: genes in the biofilm circuit are significantly weighted toward genes that arose relatively recently with ancient genes being underrepresented. This circuit provides a framework for understanding many aspects of biofilm formation by C. albicans in a mammalian host. It also provides insights into how complex cell behaviors can arise from the evolution of transcription circuits. |
| Author | Nett, Jeniel E. Andes, David R. Mitrovich, Quinn M. Johnson, Alexander D. Sorrells, Trevor R. Nobile, Clarissa J. Hernday, Aaron D. Tuch, Brian B. Fox, Emily P. |
| AuthorAffiliation | 1 Department of Microbiology and Immunology, University of California-San Francisco, San Francisco, CA, USA 2 Tetrad Program, Department of Biochemistry and Biophysics, University of California-San Francisco, San Francisco, CA, USA 3 Department of Medicine, University of Wisconsin, Madison, WI, USA |
| AuthorAffiliation_xml | – name: 2 Tetrad Program, Department of Biochemistry and Biophysics, University of California-San Francisco, San Francisco, CA, USA – name: 3 Department of Medicine, University of Wisconsin, Madison, WI, USA – name: 1 Department of Microbiology and Immunology, University of California-San Francisco, San Francisco, CA, USA |
| Author_xml | – sequence: 1 givenname: Clarissa J. surname: Nobile fullname: Nobile, Clarissa J. email: clarissa.nobile@ucsf.edu organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 2 givenname: Emily P. surname: Fox fullname: Fox, Emily P. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 3 givenname: Jeniel E. surname: Nett fullname: Nett, Jeniel E. organization: Department of Medicine, University of Wisconsin, Madison, WI 53706, USA – sequence: 4 givenname: Trevor R. surname: Sorrells fullname: Sorrells, Trevor R. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 5 givenname: Quinn M. surname: Mitrovich fullname: Mitrovich, Quinn M. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 6 givenname: Aaron D. surname: Hernday fullname: Hernday, Aaron D. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 7 givenname: Brian B. surname: Tuch fullname: Tuch, Brian B. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA – sequence: 8 givenname: David R. surname: Andes fullname: Andes, David R. organization: Department of Medicine, University of Wisconsin, Madison, WI 53706, USA – sequence: 9 givenname: Alexander D. surname: Johnson fullname: Johnson, Alexander D. organization: Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94102, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22265407$$D View this record in MEDLINE/PubMed |
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| Notes | http://dx.doi.org/10.1016/j.cell.2011.10.048 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 Current Address: Amyris, Emeryville, CA, USA Current Address: Genome Analysis Unit, Amgen, South San Francisco, CA, USA |
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| Snippet | A biofilm is an organized, resilient group of microbes in which individual cells acquire properties, such as drug resistance, that are distinct from those... A biofilm is an organized, resilient group of microbes where individual cells acquire properties, such as drug resistance, that are distinct from those... |
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| SubjectTerms | animal models Animals biofilm Biofilms - growth & development Candida albicans Candida albicans - genetics Candida albicans - physiology Candida albicans - ultrastructure Candidiasis, Oral - microbiology Candidiasis, Vulvovaginal - microbiology Catheter-Related Infections - microbiology Disease Models, Animal drug resistance evolution Evolution, Molecular Female Gene Expression Profiling Gene Expression Regulation, Fungal Gene Regulatory Networks genes Genes, Fungal Male mammals Microscopy, Confocal Rats Rats, Sprague-Dawley Stomatitis, Denture - microbiology transcription (genetics) transcription factors yeasts |
| Title | A Recently Evolved Transcriptional Network Controls Biofilm Development in Candida albicans |
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