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A common vesicle proteome drives fungal biofilm development
Extracellular vesicles mediate community interactions among cells ranging from unicellular microbes to complex vertebrates. Extracellular vesicles of the fungal pathogen Candida albicans are vital for biofilm communities to produce matrix, which confers environmental protection and modulates communi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501958/ https://www.ncbi.nlm.nih.gov/pubmed/36095193 http://dx.doi.org/10.1073/pnas.2211424119 |
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author | Zarnowski, Robert Sanchez, Hiram Jaromin, Anna Zarnowska, Urszula J. Nett, Jeniel E. Mitchell, Aaron P. Andes, David |
author_facet | Zarnowski, Robert Sanchez, Hiram Jaromin, Anna Zarnowska, Urszula J. Nett, Jeniel E. Mitchell, Aaron P. Andes, David |
author_sort | Zarnowski, Robert |
collection | PubMed |
description | Extracellular vesicles mediate community interactions among cells ranging from unicellular microbes to complex vertebrates. Extracellular vesicles of the fungal pathogen Candida albicans are vital for biofilm communities to produce matrix, which confers environmental protection and modulates community dispersion. Infections are increasingly due to diverse Candida species, such as the emerging pathogen Candida auris, as well as mixed Candida communities. Here, we define the composition and function of biofilm-associated vesicles among five species across the Candida genus. We find similarities in vesicle size and release over the biofilm lifespan. Whereas overall cargo proteomes differ dramatically among species, a group of 36 common proteins is enriched for orthologs of C. albicans biofilm mediators. To understand the function of this set of proteins, we asked whether mutants in select components were important for key biofilm processes, including drug tolerance and dispersion. We found that the majority of these cargo components impact one or both biofilm processes across all five species. Exogenous delivery of wild-type vesicle cargo returned mutant phenotypes toward wild type. To assess the impact of vesicle cargo on interspecies interactions, we performed cross-species vesicle addition and observed functional complementation for both biofilm phenotypes. We explored the biologic relevance of this cross-species biofilm interaction in mixed species and mutant studies examining the drug-resistance phenotype. We found a majority of biofilm interactions among species restored the community’s wild-type behavior. Our studies indicate that vesicles influence the development of protective monomicrobial and mixed microbial biofilm communities. |
format | Online Article Text |
id | pubmed-9501958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-95019582022-09-24 A common vesicle proteome drives fungal biofilm development Zarnowski, Robert Sanchez, Hiram Jaromin, Anna Zarnowska, Urszula J. Nett, Jeniel E. Mitchell, Aaron P. Andes, David Proc Natl Acad Sci U S A Biological Sciences Extracellular vesicles mediate community interactions among cells ranging from unicellular microbes to complex vertebrates. Extracellular vesicles of the fungal pathogen Candida albicans are vital for biofilm communities to produce matrix, which confers environmental protection and modulates community dispersion. Infections are increasingly due to diverse Candida species, such as the emerging pathogen Candida auris, as well as mixed Candida communities. Here, we define the composition and function of biofilm-associated vesicles among five species across the Candida genus. We find similarities in vesicle size and release over the biofilm lifespan. Whereas overall cargo proteomes differ dramatically among species, a group of 36 common proteins is enriched for orthologs of C. albicans biofilm mediators. To understand the function of this set of proteins, we asked whether mutants in select components were important for key biofilm processes, including drug tolerance and dispersion. We found that the majority of these cargo components impact one or both biofilm processes across all five species. Exogenous delivery of wild-type vesicle cargo returned mutant phenotypes toward wild type. To assess the impact of vesicle cargo on interspecies interactions, we performed cross-species vesicle addition and observed functional complementation for both biofilm phenotypes. We explored the biologic relevance of this cross-species biofilm interaction in mixed species and mutant studies examining the drug-resistance phenotype. We found a majority of biofilm interactions among species restored the community’s wild-type behavior. Our studies indicate that vesicles influence the development of protective monomicrobial and mixed microbial biofilm communities. National Academy of Sciences 2022-09-12 2022-09-20 /pmc/articles/PMC9501958/ /pubmed/36095193 http://dx.doi.org/10.1073/pnas.2211424119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Zarnowski, Robert Sanchez, Hiram Jaromin, Anna Zarnowska, Urszula J. Nett, Jeniel E. Mitchell, Aaron P. Andes, David A common vesicle proteome drives fungal biofilm development |
title | A common vesicle proteome drives fungal biofilm development |
title_full | A common vesicle proteome drives fungal biofilm development |
title_fullStr | A common vesicle proteome drives fungal biofilm development |
title_full_unstemmed | A common vesicle proteome drives fungal biofilm development |
title_short | A common vesicle proteome drives fungal biofilm development |
title_sort | common vesicle proteome drives fungal biofilm development |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501958/ https://www.ncbi.nlm.nih.gov/pubmed/36095193 http://dx.doi.org/10.1073/pnas.2211424119 |
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