4.6 Article

AhrC Negatively Regulates Streptococcus mutans Arginine Biosynthesis

期刊

MICROBIOLOGY SPECTRUM
卷 10, 期 4, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.00721-22

关键词

biofilm(s); Streptococcus mutans; transcription factor(s); gene expression; microbial genetics

资金

  1. National Natural Science Foundation of China [32170046, 31870065]
  2. International Research and Development Program of Sichuan [2022YFH0048, 2021YFH0060]
  3. Technological Innovation and Development Project of Chengdu Bureau of Science and Technology [2021-YF05-01819-SN]

向作者/读者索取更多资源

This study identified a transcription factor called AhrC, which negatively regulates arginine biosynthesis and biofilm formation in S. mutans. The deletion of ahrC in strains resulted in slow growth and increased intracellular arginine content, while overexpression of ahrC led to reduced arginine content, decreased biofilm and altered biofilm structures. The analysis also revealed specific DNA patterns bound by AhrC, and it acted as a negative regulator. These findings contribute to our understanding of the regulation of arginine biosynthesis and biofilm formation in S. mutans.
Streptococcus mutans is a primary cariogenic pathogen in humans. Arginine metabolism is required for bacterial growth. In S. mutans, however, the involvement of transcription factors in regulating arginine metabolism is unclear. The purpose of this study was to investigate the function and mechanism of ArgR family transcription factors in S. mutans. Here, we identified an ArgR (arginine repressor) family transcription factor named AhrC, which negatively regulates arginine biosynthesis and biofilm formation in S. mutans. The ahrC in-frame deletion strain exhibited slow growth and significantly increased intracellular arginine content. The strain overexpressing ahrC showed reduced intracellular arginine content, decreased biofilm biomass, reduced production of water-insoluble exopolysaccharides (EPS), and different biofilm structures. Furthermore, global gene expression profiles revealed differential expression levels of 233 genes in the ahrC-deficient strain, among which genes related to arginine biosynthesis (argJ, argB, argC, argD, argF, argG, argH) were significantly upregulated. In the ahrC overexpression strain, there are 89 differentially expressed genes, mostly related to arginine biosynthesis. The conserved DNA patterns bound by AhrC were identified by electrophoretic mobility shift assay (EMSA) and DNase I footprinting. In addition, the analysis of beta-galactosidase activity showed that AhrC acted as a negative regulator. Taken together, our findings suggest that AhrC is an important transcription factor that regulates arginine biosynthesis gene expression and biofilm formation in S. mutans. These findings add new aspects to the complexity of regulating the expression of genes involved in arginine biosynthesis and biofilm formation in S. mutans. IMPORTANCE Arginine metabolism is essential for bacterial growth. The regulation of intracellular arginine metabolism in Streptococcus mutans, one of the major pathogens of dental caries, is unclear. In this study, we found that the transcription factor AhrC can directly and negatively regulate the expression of N-acetyl-gamma-glutamyl-phosphate reductase (argC), thus regulating arginine biosynthesis in S. mutans. In addition, the ahrC overexpression strain exhibited a significant decrease in biofilm and water-insoluble extracellular polysaccharides (EPS). This study adds new support to our understanding of the regulation of intracellular arginine metabolism in S. mutans.

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