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Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp

Coccidioides immitis and C. posadasii, the causative agents of coccidioidomycosis, are dimorphic fungal pathogens, which grow as hyphae in the saprobic phase in the environment and as spherules in the parasitic phase in the mammalian host. In this study, we use comparative transcriptomics to identif...

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Autores principales: Whiston, Emily, Zhang Wise, Hua, Sharpton, Thomas J., Jui, Ginger, Cole, Garry T., Taylor, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401177/
https://www.ncbi.nlm.nih.gov/pubmed/22911737
http://dx.doi.org/10.1371/journal.pone.0041034
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author Whiston, Emily
Zhang Wise, Hua
Sharpton, Thomas J.
Jui, Ginger
Cole, Garry T.
Taylor, John W.
author_facet Whiston, Emily
Zhang Wise, Hua
Sharpton, Thomas J.
Jui, Ginger
Cole, Garry T.
Taylor, John W.
author_sort Whiston, Emily
collection PubMed
description Coccidioides immitis and C. posadasii, the causative agents of coccidioidomycosis, are dimorphic fungal pathogens, which grow as hyphae in the saprobic phase in the environment and as spherules in the parasitic phase in the mammalian host. In this study, we use comparative transcriptomics to identify gene expression differences between the saprobic and parasitic growth phases. We prepared Illumina mRNA sequencing libraries for saprobic-phase hyphae and parasitic-phase spherules in vitro for C. immitis isolate RS and C. posadasii isolate C735 in biological triplicate. Of 9,910 total predicted genes in Coccidioides, we observed 1,298 genes up-regulated in the saprobic phase of both C. immitis and C. posadasii and 1,880 genes up-regulated in the parasitic phase of both species. Comparing the saprobic and parasitic growth phases, we observed considerable differential expression of cell surface-associated genes, particularly chitin-related genes. We also observed differential expression of several virulence factors previously identified in Coccidioides and other dimorphic fungal pathogens. These included alpha (1,3) glucan synthase, SOWgp, and several genes in the urease pathway. Furthermore, we observed differential expression in many genes predicted to be under positive selection in two recent Coccidioides comparative genomics studies. These results highlight a number of genes that may be crucial to dimorphic phase-switching and virulence in Coccidioides. These observations will impact priorities for future genetics-based studies in Coccidioides and provide context for studies in other fungal pathogens.
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spelling pubmed-34011772012-07-30 Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp Whiston, Emily Zhang Wise, Hua Sharpton, Thomas J. Jui, Ginger Cole, Garry T. Taylor, John W. PLoS One Research Article Coccidioides immitis and C. posadasii, the causative agents of coccidioidomycosis, are dimorphic fungal pathogens, which grow as hyphae in the saprobic phase in the environment and as spherules in the parasitic phase in the mammalian host. In this study, we use comparative transcriptomics to identify gene expression differences between the saprobic and parasitic growth phases. We prepared Illumina mRNA sequencing libraries for saprobic-phase hyphae and parasitic-phase spherules in vitro for C. immitis isolate RS and C. posadasii isolate C735 in biological triplicate. Of 9,910 total predicted genes in Coccidioides, we observed 1,298 genes up-regulated in the saprobic phase of both C. immitis and C. posadasii and 1,880 genes up-regulated in the parasitic phase of both species. Comparing the saprobic and parasitic growth phases, we observed considerable differential expression of cell surface-associated genes, particularly chitin-related genes. We also observed differential expression of several virulence factors previously identified in Coccidioides and other dimorphic fungal pathogens. These included alpha (1,3) glucan synthase, SOWgp, and several genes in the urease pathway. Furthermore, we observed differential expression in many genes predicted to be under positive selection in two recent Coccidioides comparative genomics studies. These results highlight a number of genes that may be crucial to dimorphic phase-switching and virulence in Coccidioides. These observations will impact priorities for future genetics-based studies in Coccidioides and provide context for studies in other fungal pathogens. Public Library of Science 2012-07-20 /pmc/articles/PMC3401177/ /pubmed/22911737 http://dx.doi.org/10.1371/journal.pone.0041034 Text en Whiston et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Whiston, Emily
Zhang Wise, Hua
Sharpton, Thomas J.
Jui, Ginger
Cole, Garry T.
Taylor, John W.
Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title_full Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title_fullStr Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title_full_unstemmed Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title_short Comparative Transcriptomics of the Saprobic and Parasitic Growth Phases in Coccidioides spp
title_sort comparative transcriptomics of the saprobic and parasitic growth phases in coccidioides spp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401177/
https://www.ncbi.nlm.nih.gov/pubmed/22911737
http://dx.doi.org/10.1371/journal.pone.0041034
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