Discovery of a "white-gray-opaque" tristable phenotypic switching system in candida albicans: roles of non-genetic diversity in host adaptation

Non-genetic phenotypic variations play a critical role in the adaption to environmental changes in microbial organisms. Candida albicans, a major human fungal pathogen, can switch between several morphological phenotypes. This ability is critical for its commensal lifestyle and for its ability to ca...

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Veröffentlicht in:PLoS biology 2014-04, Vol.12 (4), p.e1001830-e1001830
Hauptverfasser: Tao, Li, Du, Han, Guan, Guobo, Dai, Yu, Nobile, Clarissa J, Liang, Weihong, Cao, Chengjun, Zhang, Qiuyu, Zhong, Jin, Huang, Guanghua
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container_issue 4
container_start_page e1001830
container_title PLoS biology
container_volume 12
creator Tao, Li
Du, Han
Guan, Guobo
Dai, Yu
Nobile, Clarissa J
Liang, Weihong
Cao, Chengjun
Zhang, Qiuyu
Zhong, Jin
Huang, Guanghua
description Non-genetic phenotypic variations play a critical role in the adaption to environmental changes in microbial organisms. Candida albicans, a major human fungal pathogen, can switch between several morphological phenotypes. This ability is critical for its commensal lifestyle and for its ability to cause infections. Here, we report the discovery of a novel morphological form in C. albicans, referred to as the "gray" phenotype, which forms a tristable phenotypic switching system with the previously reported white and opaque phenotypes. White, gray, and opaque cell types differ in a number of aspects including cellular and colony appearances, mating competency, secreted aspartyl proteinase (Sap) activities, and virulence. Of the three cell types, gray cells exhibit the highest Sap activity and the highest ability to cause cutaneous infections. The three phenotypes form a tristable phenotypic switching system, which is independent of the regulation of the mating type locus (MTL). Gray cells mate over 1,000 times more efficiently than do white cells, but less efficiently than do opaque cells. We further demonstrate that the master regulator of white-opaque switching, Wor1, is essential for opaque cell formation, but is not required for white-gray transitions. The Efg1 regulator is required for maintenance of the white phenotype, but is not required for gray-opaque transitions. Interestingly, the wor1/wor1 efg1/efg1 double mutant is locked in the gray phenotype, suggesting that Wor1 and Efg1 could function coordinately and play a central role in the regulation of gray cell formation. Global transcriptional analysis indicates that white, gray, and opaque cells exhibit distinct gene expression profiles, which partly explain their differences in causing infections, adaptation ability to diverse host niches, metabolic profiles, and stress responses. Therefore, the white-gray-opaque tristable phenotypic switching system in C. albicans may play a significant role in a wide range of biological aspects in this common commensal and pathogenic fungus.
doi_str_mv 10.1371/journal.pbio.1001830
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Candida albicans, a major human fungal pathogen, can switch between several morphological phenotypes. This ability is critical for its commensal lifestyle and for its ability to cause infections. Here, we report the discovery of a novel morphological form in C. albicans, referred to as the "gray" phenotype, which forms a tristable phenotypic switching system with the previously reported white and opaque phenotypes. White, gray, and opaque cell types differ in a number of aspects including cellular and colony appearances, mating competency, secreted aspartyl proteinase (Sap) activities, and virulence. Of the three cell types, gray cells exhibit the highest Sap activity and the highest ability to cause cutaneous infections. The three phenotypes form a tristable phenotypic switching system, which is independent of the regulation of the mating type locus (MTL). Gray cells mate over 1,000 times more efficiently than do white cells, but less efficiently than do opaque cells. We further demonstrate that the master regulator of white-opaque switching, Wor1, is essential for opaque cell formation, but is not required for white-gray transitions. The Efg1 regulator is required for maintenance of the white phenotype, but is not required for gray-opaque transitions. Interestingly, the wor1/wor1 efg1/efg1 double mutant is locked in the gray phenotype, suggesting that Wor1 and Efg1 could function coordinately and play a central role in the regulation of gray cell formation. Global transcriptional analysis indicates that white, gray, and opaque cells exhibit distinct gene expression profiles, which partly explain their differences in causing infections, adaptation ability to diverse host niches, metabolic profiles, and stress responses. 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This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Tao L, Du H, Guan G, Dai Y, Nobile CJ, et al. (2014) Discovery of a "White-Gray-Opaque" Tristable Phenotypic Switching System in Candida albicans: Roles of Non-genetic Diversity in Host Adaptation. 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We further demonstrate that the master regulator of white-opaque switching, Wor1, is essential for opaque cell formation, but is not required for white-gray transitions. The Efg1 regulator is required for maintenance of the white phenotype, but is not required for gray-opaque transitions. Interestingly, the wor1/wor1 efg1/efg1 double mutant is locked in the gray phenotype, suggesting that Wor1 and Efg1 could function coordinately and play a central role in the regulation of gray cell formation. Global transcriptional analysis indicates that white, gray, and opaque cells exhibit distinct gene expression profiles, which partly explain their differences in causing infections, adaptation ability to diverse host niches, metabolic profiles, and stress responses. 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phenotype</subject><subject>Grants</subject><subject>Host-Pathogen Interactions</subject><subject>Infections</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Microbiological research</subject><subject>Phenotype</subject><subject>Scanning electron microscopy</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><issn>1545-7885</issn><issn>1544-9173</issn><issn>1545-7885</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVk9tu1DAQhiMEoqXwBgiscgMXWRwnzoELpKqcVqqoxOnWmjjjrKusndreljwFr4zDbquuxAUoF7bG3_97PJNJkqcZXWR5lb2-sBtnYFiMrbaLjNKszum95DDjBU-ruub37-wPkkfeX1DKWMPqh8kBK8omSvhh8uud9tJeoZuIVQTI8fVKB0x7B1NqR7jc4DEJTvsA7YBkXKGxYRq1JP5aB7nSpid-8gHXRBsiwXS6AwJDq-PevyHODuhnZ2NN2qPBEKWdjvd5HaZZs7I-EOhgDBC0NY-TBwoGj09261Hy_cP7b6ef0rPzj8vTk7NUlmUV0hIoVFwyDiAhZ4rXTcszmktosa5iKSTPlaS0qwvVMcWatsoxRloZq5FJzI-S51vfcbBe7GrpRcYZZ01Tcx6J5ZboLFyI0ek1uElY0OJPwLpegIvPGVCUbaeqpmlrVZUF60rgrFQUJZUIBcoyer3d3bZp19hJNMHBsGe6f2L0SvT2SuRNxWg9J_NyZ-Bs7IkPYh37hsMABu1mzjtjnDdNNaMvtmgPMTVtlI2OcsbFSR7_kaJqaBWpxV-o-HW41tIaVDrG9wSv9gSRCfgz9LDxXiy_fvkP9vO_s-c_9tliy0pnvXeobiuYUTEPxU0jxTwUYjcUUfbsbvVvRTdTkP8GZPULVQ</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Tao, Li</creator><creator>Du, Han</creator><creator>Guan, Guobo</creator><creator>Dai, Yu</creator><creator>Nobile, Clarissa J</creator><creator>Liang, Weihong</creator><creator>Cao, Chengjun</creator><creator>Zhang, Qiuyu</creator><creator>Zhong, Jin</creator><creator>Huang, Guanghua</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>CZG</scope></search><sort><creationdate>20140401</creationdate><title>Discovery of a "white-gray-opaque" tristable phenotypic switching system in candida albicans: roles of non-genetic diversity in host adaptation</title><author>Tao, Li ; 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Candida albicans, a major human fungal pathogen, can switch between several morphological phenotypes. This ability is critical for its commensal lifestyle and for its ability to cause infections. Here, we report the discovery of a novel morphological form in C. albicans, referred to as the "gray" phenotype, which forms a tristable phenotypic switching system with the previously reported white and opaque phenotypes. White, gray, and opaque cell types differ in a number of aspects including cellular and colony appearances, mating competency, secreted aspartyl proteinase (Sap) activities, and virulence. Of the three cell types, gray cells exhibit the highest Sap activity and the highest ability to cause cutaneous infections. The three phenotypes form a tristable phenotypic switching system, which is independent of the regulation of the mating type locus (MTL). Gray cells mate over 1,000 times more efficiently than do white cells, but less efficiently than do opaque cells. We further demonstrate that the master regulator of white-opaque switching, Wor1, is essential for opaque cell formation, but is not required for white-gray transitions. The Efg1 regulator is required for maintenance of the white phenotype, but is not required for gray-opaque transitions. Interestingly, the wor1/wor1 efg1/efg1 double mutant is locked in the gray phenotype, suggesting that Wor1 and Efg1 could function coordinately and play a central role in the regulation of gray cell formation. Global transcriptional analysis indicates that white, gray, and opaque cells exhibit distinct gene expression profiles, which partly explain their differences in causing infections, adaptation ability to diverse host niches, metabolic profiles, and stress responses. Therefore, the white-gray-opaque tristable phenotypic switching system in C. albicans may play a significant role in a wide range of biological aspects in this common commensal and pathogenic fungus.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24691005</pmid><doi>10.1371/journal.pbio.1001830</doi><oa>free_for_read</oa></addata></record>
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subjects Acetylglucosamine - metabolism
Adaptation, Physiological - physiology
Animals
Aspartic Acid Proteases - biosynthesis
Aspartic Acid Proteases - genetics
Biological diversity
Biology and Life Sciences
Candida albicans
Candida albicans - genetics
Candida albicans - pathogenicity
Candida albicans - physiology
Candidiasis - pathology
Carbon Dioxide - metabolism
Colonies & territories
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Fungal Proteins - genetics
Fungal Proteins - metabolism
Gene expression
Gene Expression Regulation, Fungal
Genes, Mating Type, Fungal
Genetic aspects
Genetic diversity
Genetic research
Genetic Variation
Genotype & phenotype
Grants
Host-Pathogen Interactions
Infections
Medicine and Health Sciences
Mice
Microbiological research
Phenotype
Scanning electron microscopy
Transcription Factors - genetics
Transcription Factors - metabolism
title Discovery of a "white-gray-opaque" tristable phenotypic switching system in candida albicans: roles of non-genetic diversity in host adaptation
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