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LiaS调节变形链球菌中毒力因子的表达。

LiaS regulates virulence factor expression in Streptococcus mutans.

作者信息

Chong Patrick, Drake Laura, Biswas Indranil

机构信息

Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

出版信息

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

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. 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.

摘要

变形链球菌是导致龋齿形成的主要口腔病原体,它拥有多种在人类口腔中生存的机制,而口腔外部环境条件多样且处于不断变化的状态。生物膜的形成、在酸性pH条件下的存活以及变链菌素的产生被认为是该生物体展示的重要毒力决定因素。GbpC的产生促进了生物膜的形成,GbpC是一种重要的细胞表面相关蛋白,它能与葡聚糖结合,葡聚糖是该生物体自身产生的一种粘附多糖。为了更好地理解诱导GbpC产生的环境信号的本质,我们研究了14种传感器激酶在变形链球菌UA159菌株中gbpC表达中的作用。我们发现只有LiaS传感器激酶调节gbpC的表达,而其他传感器激酶对gbpC的表达几乎没有影响。我们还发现,虽然LiaS负向调节gbpC的表达,但其同源应答调节因子LiaR的失活似乎并不影响gbpC的表达。由于gbpC的表达和变链菌素IV的产生都受一个共同调控网络的调节,我们还测试了liaS突变对变链菌素产生的影响,发现LiaS正向调节变链菌素IV的产生。此外,逆转录 - PCR分析表明,LiaS通过调节nlmA和nlmT的表达来实现这一点,nlmA编码变链菌素IV的一个肽组分,nlmT编码一种ABC转运蛋白。与gbpC的表达情况一样,LiaR对变链菌素IV的产生没有任何明显影响。基于我们的研究结果,我们推测LiaS与一个或多个与LiaR属于同一家族的应答调节因子进行串扰,使LiaS能够调节几个编码毒力因子的基因的表达。

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