Regulation of cid and lrg expression by CcpA in Streptococcus mutans

• Published in: Microbiology (Society for General Microbiology) Vol. 165; no. 1; pp. 113 - 123
• Main Authors: Kim, Hey-Min, Waters, Anthony, Turner, Matthew E, Rice, Kelly C, Ahn, Sang-Joon
• Format: Journal Article
• Language: English
• Published: England Microbiology Society 01.01.2019
• Subjects: Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Gene Expression Regulation, Bacterial; Glucose - metabolism; Operon; Promoter Regions, Genetic; Repressor Proteins - genetics; Repressor Proteins - metabolism; Streptococcus mutans - genetics; Streptococcus mutans - metabolism; Cid and Lrg; glucose metabolism; CcpA; Streptococcus mutans
• ISSN: 1350-0872; 1465-2080
• DOI: 10.1099/mic.0.000744

The Streptococcus mutans Cid/Lrg system represents an ideal model for studying this organism's ability to withstand various stressors encountered in the oral cavity. The lrg and cid operons display distinct and opposite patterns of expression in response to growth phase and glucose levels, suggesting that the activity and regulation of these proteins must be tightly coordinated in the cell and closely associated with metabolic pathways of the organism. Here, we demonstrate that expression of the cid and lrg operons is directly mediated by a global transcriptional regulator CcpA in response to glucose levels. Comparison of the cid and lrg promoter regions with the conserved CcpA binding motif revealed the presence of two potential cre sites (for CcpA binding) in the cid promoter (designated cid-cre1 and cid-cre2), which were arranged in a similar manner to those previously identified in the lrg promoter region (designated lrg-cre1 and lrg-cre2). We demonstrated that CcpA binds to both the cid and lrg promoters with a high affinity, but has an opposing glucose-dependent effect on the regulation of cid (positive) and lrg (negative) expression. DNase I footprinting analyses revealed potential binding sequences for CcpA in both cid and lrg promoter regions. Collectively, these data suggest that CcpA is a direct regulator of cid and lrg expression, and are suggestive of a potential mechanism by which Cid/Lrg-mediated virulence and cellular homeostasis is integrated with signals associated with both the environment and cellular metabolic status.