Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The . gov means it’s official. Federal government websites often end in . gov or VSports app下载. mil. Before sharing sensitive information, make sure you’re on a federal government site. .

Https

The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. V体育官网.

. 2008 Jul;76(7):3093-9.
doi: 10.1128/IAI.01627-07. Epub 2008 May 5.

LiaS regulates virulence factor expression in Streptococcus mutans

Affiliations

"V体育平台登录" LiaS regulates virulence factor expression in Streptococcus mutans

Patrick Chong et al. Infect Immun. 2008 Jul.

Abstract

Streptococcus mutans, a major oral pathogen responsible for dental caries formation, possesses a variety of mechanisms for survival in the human oral cavity, where the conditions of the external environment are diverse and in a constant state of flux. The formation of biofilms, survival under conditions of acidic pH, and production of mutacins are considered to be important virulence determinants displayed by this organism. Biofilm formation is facilitated by the production of GbpC, an important cell surface-associated protein that binds to glucan, an adhesive polysaccharide produced by the organism itself. To better understand the nature of the environmental cues that induce GbpC production, we examined the roles of 14 sensor kinases in the expression of gbpC in S. mutans strain UA159. We found that only the LiaS sensor kinase regulates gbpC expression, while the other sensor kinases had little or no effect on gbpC expression. We also found that while LiaS negatively regulates gbpC expression, the inactivation of its cognate response regulator, LiaR, does not appear to affect the expression of gbpC. Since both gbpC expression and mutacin IV production are regulated by a common regulatory network, we also tested the effect of the liaS mutation on mutacin production and found that LiaS positively regulates mutacin IV production. Furthermore, reverse transcription-PCR analysis suggests that LiaS does so by regulating the expression of nlmA, which encodes a peptide component of mutacin IV, and nlmT, which encodes an ABC transporter. As with the expression of gbpC, LiaR did not have any apparent effect on mutacin IV production VSports手机版. Based on the results of our study, we speculate that LiaS is engaged in cross talk with one or more response regulators belonging to the same family as LiaR, enabling LiaS to regulate the expression of several genes coding for virulence factors. .

PubMed Disclaimer

Figures

FIG. 1.
FIG. 1.
Expression from PgbpC-gusA in the sensor kinase mutants. Fourteen different sensor kinases were inactivated in IBS131 in order to measure their effect on PgbpC-gusA expression. Strains were grown in THY broth at 37°C and harvested at the mid-exponential phase, and gusA activity was measured. The values were normalized with Gus activity obtained with IBS131. Experiments were repeated at least twice, and the mean values are shown.
FIG. 2.
FIG. 2.
Schematic diagram illustrating the deletions performed on the loci coding for the SMu486/SMu487 TCS in S. mutans UA159. Open reading frames and orientations of transcription are indicated with block arrows. The locations of the DNA sequence fragments that were used for insertion mutagenesis (pIB14) and construction of the complementing plasmid pIB55 are indicated by horizontal lines below SMu486/SMu487. The SMu486, SMu487, and SMu486/SMu487 genes were deleted and replaced with the spectinomycin resistance gene aad (Sp).
FIG. 3.
FIG. 3.
Regulation of gbpC expression by SMu486/SMu487. (A) Expression from PgbpC-gusA was measured for the wild type, (IBS131); the ΔSMu486 (IBS151), ΔSMu487 (IBS152), and ΔSMu486/SMu487 (IBS155) strains; the ΔSMu486 strain complemented with pIB55 (IBS151/pIB55); and the single-crossover ΔSMu486 strain (IBS339). Experiments were performed in triplicate, and the mean values with standard deviations are shown. (B) Expression from PgbpC-gusA was measured with the wild-type strain (IBS131) containing either pIB169 or pIB181, as described in the text. Experiments were performed in triplicate, and the mean values with standard deviations are shown. (C) Semiquantitative RT-PCR results showing the expression of gbpC from the wild type (UA159), the ΔSMu486 mutant (IBS148), the ΔSMu487 mutant (IBS149), and the ΔSMu486 mutant complemented with pIB55 (IBS148/pIB55). The data are representative of RT-PCR analyses resulting from at least two different RNA isolations.
FIG. 4.
FIG. 4.
Regulation of mutacin IV production by SMu486 in S. mutans. (A) Deferred antagonism assay for mutacin IV production. S. mutans cultures were stabbed into THY agar and incubated overnight at 37°C under microaerophilic conditions. The plates were overlaid with soft agar containing the indicator strain. The zone of inhibition of the indicator strains was evaluated after overnight incubation. (B) Semiquantitative RT-PCR results showing the expression of nlmA and nlmT by the wild type (UA159), the ΔSMu486 mutant (IBS148), and the ΔSMu486 mutant complemented with pIB55 (IBS148/pIB55). The data are representative of RT-PCR analyses resulting from at least two different RNA isolations.

References

    1. Ajdic, D., W. M. McShan, R. E. McLaughlin, G. Savic, J. Chang, M. B. Carson, C. Primeaux, R. Tian, S. Kenton, H. Jia, S. Lin, Y. Qian, S. Li, H. Zhu, F. Najar, H. Lai, J. White, B. A. Roe, and J. J. Ferretti. 2002. Genome sequence of Streptococcus mutans UA159, a cariogenic dental pathogen. Proc. Natl. Acad. Sci. USA 9914434-14439. - PMC - PubMed
    1. Ashby, M. K. 2004. Survey of the number of two-component response regulator genes in the complete and annotated genome sequences of prokaryotes. FEMS Microbiol. Lett. 231277-281. - PubMed
    1. Banas, J. A. 2004. Virulence properties of Streptococcus mutans. Front. Biosci. 91267-1277. - PubMed (V体育官网)
    1. Banas, J. A., R. R. Russell, and J. J. Ferretti. 1990. Sequence analysis of the gene for the glucan-binding protein of Streptococcus mutans Ingbritt. Infect. Immun. 58667-673. - PMC (VSports) - PubMed
    1. Banas, J. A., and M. M. Vickerman. 2003. Glucan-binding proteins of the oral streptococci. Crit. Rev. Oral Biol. Med. 1489-99. - PubMed

Publication types

MeSH terms