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DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness

BACKGROUND: A biofilm is a complex community of microorganisms that develop on surfaces in diverse environments. The thickness of the biofilm plays a crucial role in the physiology of the immobilized bacteria. The most cariogenic bacteria, mutans streptococci, are common inhabitants of a dental biof...

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Autores principales: Shemesh, Moshe, Tam, Avshalom, Kott-Gutkowski, Miriam, Feldman, Mark, Steinberg, Doron
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647549/
https://www.ncbi.nlm.nih.gov/pubmed/19114020
http://dx.doi.org/10.1186/1471-2180-8-236
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author Shemesh, Moshe
Tam, Avshalom
Kott-Gutkowski, Miriam
Feldman, Mark
Steinberg, Doron
author_facet Shemesh, Moshe
Tam, Avshalom
Kott-Gutkowski, Miriam
Feldman, Mark
Steinberg, Doron
author_sort Shemesh, Moshe
collection PubMed
description BACKGROUND: A biofilm is a complex community of microorganisms that develop on surfaces in diverse environments. The thickness of the biofilm plays a crucial role in the physiology of the immobilized bacteria. The most cariogenic bacteria, mutans streptococci, are common inhabitants of a dental biofilm community. In this study, DNA-microarray analysis was used to identify differentially expressed genes associated with the thickness of S. mutans biofilms. RESULTS: Comparative transcriptome analyses indicated that expression of 29 genes was differentially altered in 400- vs. 100-microns depth and 39 genes in 200- vs. 100-microns biofilms. Only 10 S. mutans genes showed differential expression in both 400- vs. 100-microns and 200- vs. 100-microns biofilms. All of these genes were upregulated. As sucrose is a predominant factor in oral biofilm development, its influence was evaluated on selected genes expression in the various depths of biofilms. The presence of sucrose did not noticeably change the regulation of these genes in 400- vs. 100-microns and/or 200- vs. 100-microns biofilms tested by real-time RT-PCR. Furthermore, we analyzed the expression profile of selected biofilm thickness associated genes in the luxS(- )mutant strain. The expression of those genes was not radically changed in the mutant strain compared to wild-type bacteria in planktonic condition. Only slight downregulation was recorded in SMU.2146c, SMU.574, SMU.609, and SMU.987 genes expression in luxS(- )bacteria in biofilm vs. planktonic environments. CONCLUSION: These findings reveal genes associated with the thickness of biofilms of S. mutans. Expression of these genes is apparently not regulated directly by luxS and is not necessarily influenced by the presence of sucrose in the growth media.
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spelling pubmed-26475492009-02-25 DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness Shemesh, Moshe Tam, Avshalom Kott-Gutkowski, Miriam Feldman, Mark Steinberg, Doron BMC Microbiol Research Article BACKGROUND: A biofilm is a complex community of microorganisms that develop on surfaces in diverse environments. The thickness of the biofilm plays a crucial role in the physiology of the immobilized bacteria. The most cariogenic bacteria, mutans streptococci, are common inhabitants of a dental biofilm community. In this study, DNA-microarray analysis was used to identify differentially expressed genes associated with the thickness of S. mutans biofilms. RESULTS: Comparative transcriptome analyses indicated that expression of 29 genes was differentially altered in 400- vs. 100-microns depth and 39 genes in 200- vs. 100-microns biofilms. Only 10 S. mutans genes showed differential expression in both 400- vs. 100-microns and 200- vs. 100-microns biofilms. All of these genes were upregulated. As sucrose is a predominant factor in oral biofilm development, its influence was evaluated on selected genes expression in the various depths of biofilms. The presence of sucrose did not noticeably change the regulation of these genes in 400- vs. 100-microns and/or 200- vs. 100-microns biofilms tested by real-time RT-PCR. Furthermore, we analyzed the expression profile of selected biofilm thickness associated genes in the luxS(- )mutant strain. The expression of those genes was not radically changed in the mutant strain compared to wild-type bacteria in planktonic condition. Only slight downregulation was recorded in SMU.2146c, SMU.574, SMU.609, and SMU.987 genes expression in luxS(- )bacteria in biofilm vs. planktonic environments. CONCLUSION: These findings reveal genes associated with the thickness of biofilms of S. mutans. Expression of these genes is apparently not regulated directly by luxS and is not necessarily influenced by the presence of sucrose in the growth media. BioMed Central 2008-12-29 /pmc/articles/PMC2647549/ /pubmed/19114020 http://dx.doi.org/10.1186/1471-2180-8-236 Text en Copyright © 2008 Shemesh et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shemesh, Moshe
Tam, Avshalom
Kott-Gutkowski, Miriam
Feldman, Mark
Steinberg, Doron
DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title_full DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title_fullStr DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title_full_unstemmed DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title_short DNA-microarrays identification of Streptococcus mutans genes associated with biofilm thickness
title_sort dna-microarrays identification of streptococcus mutans genes associated with biofilm thickness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647549/
https://www.ncbi.nlm.nih.gov/pubmed/19114020
http://dx.doi.org/10.1186/1471-2180-8-236
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