Cargando…

Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum

Candida albicans and Fusobacterium nucleatum are well-studied oral commensal microbes with pathogenic potential that are involved in various oral polymicrobial infectious diseases. Recently, we demonstrated that F. nucleatum ATCC 23726 coaggregates with C. albicans SN152, a process mainly mediated b...

Descripción completa

Detalles Bibliográficos
Autores principales: Bor, Batbileg, Cen, Lujia, Agnello, Melissa, Shi, Wenyuan, He, Xuesong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906402/
https://www.ncbi.nlm.nih.gov/pubmed/27295972
http://dx.doi.org/10.1038/srep27956
_version_ 1782437415037698048
author Bor, Batbileg
Cen, Lujia
Agnello, Melissa
Shi, Wenyuan
He, Xuesong
author_facet Bor, Batbileg
Cen, Lujia
Agnello, Melissa
Shi, Wenyuan
He, Xuesong
author_sort Bor, Batbileg
collection PubMed
description Candida albicans and Fusobacterium nucleatum are well-studied oral commensal microbes with pathogenic potential that are involved in various oral polymicrobial infectious diseases. Recently, we demonstrated that F. nucleatum ATCC 23726 coaggregates with C. albicans SN152, a process mainly mediated by fusobacterial membrane protein RadD and Candida cell wall protein Flo9. The aim of this study was to investigate the potential biological impact of this inter-kingdom interaction. We found that F. nucleatum ATCC 23726 inhibits growth and hyphal morphogenesis of C. albicans SN152 in a contact-dependent manner. Further analysis revealed that the inhibition of Candida hyphal morphogenesis is mediated via RadD and Flo9 protein pair. Using a murine macrophage cell line, we showed that the F. nucleatum-induced inhibition of Candida hyphal morphogenesis promotes C. albicans survival and negatively impacts the macrophage-killing capability of C. albicans. Furthermore, the yeast form of C. albicans repressed F. nucleatum-induced MCP-1 and TNFα production in macrophages. Our study suggests that the interaction between C. albicans and F. nucleatum leads to a mutual attenuation of virulence, which may function to promote a long-term commensal lifestyle within the oral cavity. This finding has significant implications for our understanding of inter-kingdom interaction and may impact clinical treatment strategies.
format Online
Article
Text
id pubmed-4906402
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49064022016-06-15 Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum Bor, Batbileg Cen, Lujia Agnello, Melissa Shi, Wenyuan He, Xuesong Sci Rep Article Candida albicans and Fusobacterium nucleatum are well-studied oral commensal microbes with pathogenic potential that are involved in various oral polymicrobial infectious diseases. Recently, we demonstrated that F. nucleatum ATCC 23726 coaggregates with C. albicans SN152, a process mainly mediated by fusobacterial membrane protein RadD and Candida cell wall protein Flo9. The aim of this study was to investigate the potential biological impact of this inter-kingdom interaction. We found that F. nucleatum ATCC 23726 inhibits growth and hyphal morphogenesis of C. albicans SN152 in a contact-dependent manner. Further analysis revealed that the inhibition of Candida hyphal morphogenesis is mediated via RadD and Flo9 protein pair. Using a murine macrophage cell line, we showed that the F. nucleatum-induced inhibition of Candida hyphal morphogenesis promotes C. albicans survival and negatively impacts the macrophage-killing capability of C. albicans. Furthermore, the yeast form of C. albicans repressed F. nucleatum-induced MCP-1 and TNFα production in macrophages. Our study suggests that the interaction between C. albicans and F. nucleatum leads to a mutual attenuation of virulence, which may function to promote a long-term commensal lifestyle within the oral cavity. This finding has significant implications for our understanding of inter-kingdom interaction and may impact clinical treatment strategies. Nature Publishing Group 2016-06-14 /pmc/articles/PMC4906402/ /pubmed/27295972 http://dx.doi.org/10.1038/srep27956 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bor, Batbileg
Cen, Lujia
Agnello, Melissa
Shi, Wenyuan
He, Xuesong
Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title_full Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title_fullStr Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title_full_unstemmed Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title_short Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum
title_sort morphological and physiological changes induced by contact-dependent interaction between candida albicans and fusobacterium nucleatum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906402/
https://www.ncbi.nlm.nih.gov/pubmed/27295972
http://dx.doi.org/10.1038/srep27956
work_keys_str_mv AT borbatbileg morphologicalandphysiologicalchangesinducedbycontactdependentinteractionbetweencandidaalbicansandfusobacteriumnucleatum
AT cenlujia morphologicalandphysiologicalchangesinducedbycontactdependentinteractionbetweencandidaalbicansandfusobacteriumnucleatum
AT agnellomelissa morphologicalandphysiologicalchangesinducedbycontactdependentinteractionbetweencandidaalbicansandfusobacteriumnucleatum
AT shiwenyuan morphologicalandphysiologicalchangesinducedbycontactdependentinteractionbetweencandidaalbicansandfusobacteriumnucleatum
AT hexuesong morphologicalandphysiologicalchangesinducedbycontactdependentinteractionbetweencandidaalbicansandfusobacteriumnucleatum