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Identification of a signalling molecule involved in bacterial intergeneric communication

The development of complex multispecies communities such as biofilms is controlled by interbacterial communication systems. We have previously reported an intergeneric communication between two oral bacteria, Streptococcus cristatus and Porphyromonas gingivalis, that results in inhibition of fimA ex...

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Detalles Bibliográficos
Autores principales: Xie, Hua, Lin, Xinghua, Wang, Bing-Yan, Wu, Jie, Lamont, Richard J.
Formato: Texto
Lenguaje:English
Publicado: Microbiology Society 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885614/
https://www.ncbi.nlm.nih.gov/pubmed/17906122
http://dx.doi.org/10.1099/mic.0.2007/009050-0
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author Xie, Hua
Lin, Xinghua
Wang, Bing-Yan
Wu, Jie
Lamont, Richard J.
author_facet Xie, Hua
Lin, Xinghua
Wang, Bing-Yan
Wu, Jie
Lamont, Richard J.
author_sort Xie, Hua
collection PubMed
description The development of complex multispecies communities such as biofilms is controlled by interbacterial communication systems. We have previously reported an intergeneric communication between two oral bacteria, Streptococcus cristatus and Porphyromonas gingivalis, that results in inhibition of fimA expression. Here, we demonstrate that a surface protein, arginine deiminase (ArcA), of S. cristatus serves as a signal that initiates intergeneric communication. An ArcA-deficient mutant of S. cristatus is unable to communicate with P. gingivalis. Furthermore, arginase activity is not essential for the communication, and ArcA retains the ability to repress expression of fimA in the presence of arginine deiminase inhibitors. These results present a novel mechanism by which intergeneric communication in dental biofilms is accomplished.
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spelling pubmed-28856142010-07-06 Identification of a signalling molecule involved in bacterial intergeneric communication Xie, Hua Lin, Xinghua Wang, Bing-Yan Wu, Jie Lamont, Richard J. Microbiology (Reading) Pathogens and Pathogenicity The development of complex multispecies communities such as biofilms is controlled by interbacterial communication systems. We have previously reported an intergeneric communication between two oral bacteria, Streptococcus cristatus and Porphyromonas gingivalis, that results in inhibition of fimA expression. Here, we demonstrate that a surface protein, arginine deiminase (ArcA), of S. cristatus serves as a signal that initiates intergeneric communication. An ArcA-deficient mutant of S. cristatus is unable to communicate with P. gingivalis. Furthermore, arginase activity is not essential for the communication, and ArcA retains the ability to repress expression of fimA in the presence of arginine deiminase inhibitors. These results present a novel mechanism by which intergeneric communication in dental biofilms is accomplished. Microbiology Society 2007-10 /pmc/articles/PMC2885614/ /pubmed/17906122 http://dx.doi.org/10.1099/mic.0.2007/009050-0 Text en Copyright © 2007, SGM http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited.
spellingShingle Pathogens and Pathogenicity
Xie, Hua
Lin, Xinghua
Wang, Bing-Yan
Wu, Jie
Lamont, Richard J.
Identification of a signalling molecule involved in bacterial intergeneric communication
title Identification of a signalling molecule involved in bacterial intergeneric communication
title_full Identification of a signalling molecule involved in bacterial intergeneric communication
title_fullStr Identification of a signalling molecule involved in bacterial intergeneric communication
title_full_unstemmed Identification of a signalling molecule involved in bacterial intergeneric communication
title_short Identification of a signalling molecule involved in bacterial intergeneric communication
title_sort identification of a signalling molecule involved in bacterial intergeneric communication
topic Pathogens and Pathogenicity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885614/
https://www.ncbi.nlm.nih.gov/pubmed/17906122
http://dx.doi.org/10.1099/mic.0.2007/009050-0
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