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Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model
Candida albicans as an opportunistic pathogen exploits the host immune system and causes a variety of life-threatening infections. The polymorphic nature of this fungus gives it tremendous advantage to breach mucosal barriers and cause oral and disseminated infections. Similar to C. albicans, Entero...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696566/ https://www.ncbi.nlm.nih.gov/pubmed/33187237 http://dx.doi.org/10.3390/microorganisms8111771 |
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author | Krishnamoorthy, Akshaya Lakshmi Lemus, Alex A. Solomon, Adline Princy Valm, Alex M. Neelakantan, Prasanna |
author_facet | Krishnamoorthy, Akshaya Lakshmi Lemus, Alex A. Solomon, Adline Princy Valm, Alex M. Neelakantan, Prasanna |
author_sort | Krishnamoorthy, Akshaya Lakshmi |
collection | PubMed |
description | Candida albicans as an opportunistic pathogen exploits the host immune system and causes a variety of life-threatening infections. The polymorphic nature of this fungus gives it tremendous advantage to breach mucosal barriers and cause oral and disseminated infections. Similar to C. albicans, Enterococcus faecalis is a major opportunistic pathogen, which is of critical concern in immunocompromised patients. There is increasing evidence that E. faecalis co-exists with C. albicans in the human body in disease samples. While the interactive profiles between these two organisms have been studied on abiotic substrates and mouse models, studies on their interactions on human oral mucosal surfaces are non-existent. Here, for the first time, we comprehensively characterized the interactive profiles between laboratory and clinical isolates of C. albicans (SC5314 and BF1) and E. faecalis (OG1RF and P52S) on an organotypic oral mucosal model. Our results demonstrated that the dual species biofilms resulted in profound surface erosion and significantly increased microbial invasion into mucosal compartments, compared to either species alone. Notably, several genes of C. albicans involved in tissue adhesion, hyphal formation, fungal invasion, and biofilm formation were significantly upregulated in the presence of E. faecalis. By contrast, E. faecalis genes involved in quorum sensing, biofilm formation, virulence, and mammalian cell invasion were downregulated. This study highlights the synergistic cross-kingdom interactions between E. faecalis and C. albicans in mucosal tissue invasion. |
format | Online Article Text |
id | pubmed-7696566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76965662020-11-29 Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model Krishnamoorthy, Akshaya Lakshmi Lemus, Alex A. Solomon, Adline Princy Valm, Alex M. Neelakantan, Prasanna Microorganisms Article Candida albicans as an opportunistic pathogen exploits the host immune system and causes a variety of life-threatening infections. The polymorphic nature of this fungus gives it tremendous advantage to breach mucosal barriers and cause oral and disseminated infections. Similar to C. albicans, Enterococcus faecalis is a major opportunistic pathogen, which is of critical concern in immunocompromised patients. There is increasing evidence that E. faecalis co-exists with C. albicans in the human body in disease samples. While the interactive profiles between these two organisms have been studied on abiotic substrates and mouse models, studies on their interactions on human oral mucosal surfaces are non-existent. Here, for the first time, we comprehensively characterized the interactive profiles between laboratory and clinical isolates of C. albicans (SC5314 and BF1) and E. faecalis (OG1RF and P52S) on an organotypic oral mucosal model. Our results demonstrated that the dual species biofilms resulted in profound surface erosion and significantly increased microbial invasion into mucosal compartments, compared to either species alone. Notably, several genes of C. albicans involved in tissue adhesion, hyphal formation, fungal invasion, and biofilm formation were significantly upregulated in the presence of E. faecalis. By contrast, E. faecalis genes involved in quorum sensing, biofilm formation, virulence, and mammalian cell invasion were downregulated. This study highlights the synergistic cross-kingdom interactions between E. faecalis and C. albicans in mucosal tissue invasion. MDPI 2020-11-11 /pmc/articles/PMC7696566/ /pubmed/33187237 http://dx.doi.org/10.3390/microorganisms8111771 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Krishnamoorthy, Akshaya Lakshmi Lemus, Alex A. Solomon, Adline Princy Valm, Alex M. Neelakantan, Prasanna Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title | Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title_full | Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title_fullStr | Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title_full_unstemmed | Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title_short | Interactions between Candida albicans and Enterococcus faecalis in an Organotypic Oral Epithelial Model |
title_sort | interactions between candida albicans and enterococcus faecalis in an organotypic oral epithelial model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696566/ https://www.ncbi.nlm.nih.gov/pubmed/33187237 http://dx.doi.org/10.3390/microorganisms8111771 |
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