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PMID: 15336418 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

ComX activity of Streptococcus mutans growing in biofilms.

FEMS microbiology letters ·Vol. 238 ·No. 1 ·2004-09-01 ·Pages 167-74

Aspiras MB, Ellen RP, Cvitkovitch DG

Abstract

In many streptococci, including Streptococcus mutans, genetic competence is regulated by a quorum sensing system mediated by a competence stimulating peptide (CSP) pheromone, encoded by the comC gene. In Streptococcus pneumoniae, a central component of this system is ComX, which acts as an alternative sigma factor to activate competence genes involved in DNA uptake and processing. The quorum sensing system responsible for genetic competence induction in S. mutans has been linked to biofilm formation and the acid tolerance response. To examine the response of comX to CSP in S. mutans, a transcriptional fusion of the comX promoter (pcomX) with lacZ was constructed to generate reporter vector pcomx::pALH122 (replicative vector) and transformed into S. mutans UA159 comC-, which is unable to produce endogenous CSP. CSP was added and pcomX::lacZ relative expression index (REI) examined, revealing a 2-fold increase in maximal beta-gal activity 5 and 10 min after CSP addition. The effect of endogenous CSP on pcomX::lacZ expression was also examined by measuring REI in cells grown as a biofilm; peak pcomX activity was observed at 3 h. To determine the temporal pattern of transformation frequency, pMA2, a Spr shuttle vector, was transformed into biofilm-grown cells, with maximal transformation frequency observed at 3 h. Confocal microscopy was performed to examine pcomX activity using a similarly constructed green fluorescent protein reporter vector, pcomX::gfp, in a 4-h biofilm, revealing active pcomX activity in high cell density areas within the biofilm population. These results demonstrated a positive correlation between pcomX activity, natural transformation and competence development in biofilms.

MeSH Terms
Adaptation, Physiological Artificial Gene Fusion Bacterial Proteins/genetics,metabolism Biofilms/growth & development Gene Expression Regulation, Bacterial Genes, Reporter Microscopy, Confocal Plasmids Promoter Regions, Genetic Streptococcus mutans/genetics,growth & development,metabolism Time Factors Transcription Factors/genetics,metabolism Transformation, Bacterial beta-Galactosidase/genetics,metabolism
Chemicals
Bacterial Proteins ComX protein, Streptococcus Transcription Factors competence factor, Streptococcus beta-Galactosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Aspiras Marcelo B
Faculty of Dentistry, University of Toronto, 124 Edward Street, Toronto, Ont., Canada M5G 1G6.
Ellen Richard P
Cvitkovitch Dennis G
Article Info
Journal
FEMS microbiology letters
Abbr.
FEMS Microbiol Lett
ISSN
0378-1097
Published
2004-09-01
Pages
167-74
Language
English
Region
England
NLM ID
7705721
Subset
IM
Grants
NIDCR NIH HHS · R01 DE013230 · United States
NIDCR NIH HHS · R01DE013230-03 · United States
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