5331 0.0962 Figure 3 Relative quantification of eight selected genes expression during short-term hyperosmotic stress by quantitative RT-PCR. Deforolimus molecular weight Fold change of each gene expression was relative to control (without NaCl). Results were averaged from 3 independent experiments and are presented as mean ± standard deviation. *, P ≤ 0.05. It’s noteworthy that a recent transcriptomic profiling of S. mutans in the presence of oxygen also showed significant down-regulation of gtfB and genes involved in ComCDE quorum sensing system [13].
This suggests that a motile lifestyle may be a common strategy employed by S. mutans to adapt adversary conditions. S. mutans increases carbohydrates consumption in response to hyperosmotic challenge Most bacteria do not possess active water transport mechanisms to maintain cell turgor, which is essential for survival [20]. Instead, bacteria usually pool “compatible solutes” to deal with hyperosmotic conditions. Although some compatible solutes, such as glycine betaine and carnitine, can be synthesized Target Selective Inhibitor Library and accumulated intracellularly during osmotic stress, bacteria also adopt efficient transport systems to internalize necessary compounds to counter hyperosmotic
stress [6]. Burne’s previous study has suggested that S. mutans may take up compatible solutes from the environment by up-regulating the ABC transporter homologous genes (opcA and opuAA) upon short-term exposure to hyperosmotic challenge [10]. Although no significant up-regulation RNA Synthesis inhibitor of compatible solutes internalization related genes was detected by our high throughput transcriptomic profiling at a differentiation power of ≥ 2 fold changes, genes involved in the phosphotransferase system (PTS) and
carbohydrate metabolism were significantly up-regulated upon short-term hyperosmotic challenge (Table 1). We further categorized the majority of those differentially expressed genes into 12 KEGG pathways. We found that pathways involved in carbohydrates consumption, including PTS, galactose metabolism, fructose/mannose metabolism, and pyruvate metabolism were significantly up-regulated (Figure 4). Based on these findings, we propose that in order to counter the detrimental effects of short-term hyperosmotic challenge, S. mutans needs to actively internalize compatible solutes to recover from hyperosmotic stress. In the meantime, the bacterial cells have to up-regulate genes involved in carbohydrates transportation and metabolism, so as to couple the increased demand for ATP consumption. Interestingly, most of these aforementioned carbohydrates metabolism related genes and pathways are also up-regulated during oxygen challenge [13], further suggesting that S. mutans has developed sophisticated energy mobilization strategy to counter environmental adversity. Figure 4 KEGG pathway analyses for differentially expressed genes. (A) Significant up- and down-regulated pathways upon hyperosmotic challenge. P-value < 0.05 and FDR < 0.25 were used as a threshold.