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AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation
Aggregatibacter actinomycetemcomitans, a Gram-negative bacterium, and Candida albicans, a polymorphic fungus, are both commensals of the oral cavity but both are opportunistic pathogens that can cause oral diseases. A. actinomycetemcomitans produces a quorum-sensing molecule called autoinducer-2 (AI...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104835/ https://www.ncbi.nlm.nih.gov/pubmed/25101248 http://dx.doi.org/10.3389/fcimb.2014.00094 |
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author | Bachtiar, Endang W. Bachtiar, Boy M. Jarosz, Lucja M. Amir, Lisa R. Sunarto, Hari Ganin, Hadas Meijler, Michael M. Krom, Bastiaan P. |
author_facet | Bachtiar, Endang W. Bachtiar, Boy M. Jarosz, Lucja M. Amir, Lisa R. Sunarto, Hari Ganin, Hadas Meijler, Michael M. Krom, Bastiaan P. |
author_sort | Bachtiar, Endang W. |
collection | PubMed |
description | Aggregatibacter actinomycetemcomitans, a Gram-negative bacterium, and Candida albicans, a polymorphic fungus, are both commensals of the oral cavity but both are opportunistic pathogens that can cause oral diseases. A. actinomycetemcomitans produces a quorum-sensing molecule called autoinducer-2 (AI-2), synthesized by LuxS, that plays an important role in expression of virulence factors, in intra- but also in interspecies communication. The aim of this study was to investigate the role of AI-2 based signaling in the interactions between C. albicans and A. actinomycetemcomitans. A. actinomycetemcomitans adhered to C. albicans and inhibited biofilm formation by means of a molecule that was secreted during growth. C. albicans biofilm formation increased significantly when co-cultured with A. actinomycetemcomitans luxS, lacking AI-2 production. Addition of wild-type-derived spent medium or synthetic AI-2 to spent medium of the luxS strain, restored inhibition of C. albicans biofilm formation to wild-type levels. Addition of synthetic AI-2 significantly inhibited hypha formation of C. albicans possibly explaining the inhibition of biofilm formation. AI-2 of A. actinomycetemcomitans is synthesized by LuxS, accumulates during growth and inhibits C. albicans hypha- and biofilm formation. Identifying the molecular mechanisms underlying the interaction between bacteria and fungi may provide important insight into the balance within complex oral microbial communities. |
format | Online Article Text |
id | pubmed-4104835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41048352014-08-06 AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation Bachtiar, Endang W. Bachtiar, Boy M. Jarosz, Lucja M. Amir, Lisa R. Sunarto, Hari Ganin, Hadas Meijler, Michael M. Krom, Bastiaan P. Front Cell Infect Microbiol Microbiology Aggregatibacter actinomycetemcomitans, a Gram-negative bacterium, and Candida albicans, a polymorphic fungus, are both commensals of the oral cavity but both are opportunistic pathogens that can cause oral diseases. A. actinomycetemcomitans produces a quorum-sensing molecule called autoinducer-2 (AI-2), synthesized by LuxS, that plays an important role in expression of virulence factors, in intra- but also in interspecies communication. The aim of this study was to investigate the role of AI-2 based signaling in the interactions between C. albicans and A. actinomycetemcomitans. A. actinomycetemcomitans adhered to C. albicans and inhibited biofilm formation by means of a molecule that was secreted during growth. C. albicans biofilm formation increased significantly when co-cultured with A. actinomycetemcomitans luxS, lacking AI-2 production. Addition of wild-type-derived spent medium or synthetic AI-2 to spent medium of the luxS strain, restored inhibition of C. albicans biofilm formation to wild-type levels. Addition of synthetic AI-2 significantly inhibited hypha formation of C. albicans possibly explaining the inhibition of biofilm formation. AI-2 of A. actinomycetemcomitans is synthesized by LuxS, accumulates during growth and inhibits C. albicans hypha- and biofilm formation. Identifying the molecular mechanisms underlying the interaction between bacteria and fungi may provide important insight into the balance within complex oral microbial communities. Frontiers Media S.A. 2014-07-21 /pmc/articles/PMC4104835/ /pubmed/25101248 http://dx.doi.org/10.3389/fcimb.2014.00094 Text en Copyright © 2014 Bachtiar, Bachtiar, Jarosz, Amir, Sunarto, Ganin, Meijler and Krom. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Bachtiar, Endang W. Bachtiar, Boy M. Jarosz, Lucja M. Amir, Lisa R. Sunarto, Hari Ganin, Hadas Meijler, Michael M. Krom, Bastiaan P. AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title | AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title_full | AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title_fullStr | AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title_full_unstemmed | AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title_short | AI-2 of Aggregatibacter actinomycetemcomitans inhibits Candida albicans biofilm formation |
title_sort | ai-2 of aggregatibacter actinomycetemcomitans inhibits candida albicans biofilm formation |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104835/ https://www.ncbi.nlm.nih.gov/pubmed/25101248 http://dx.doi.org/10.3389/fcimb.2014.00094 |
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