SMU_1361c regulates the oxidative stress response ofStreptococcus mutans

Abstract

AbstractDental caries is the most common chronic infectious diseases around the world and disproportionately affects the marginalized socioeconomic group.Streptococcus mutans, considered a primary etiological agent of caries, must depend on the coordinated physiological response to tolerate the oxidative stress generated by commensal species within dental plaque, which is a critical aspect of its pathogenicity. Here, we identified and characterized a novel TetR family regulator SMU_1361c, encoded by the TnSmu2 operon, which appears to be acquired by the bacteria via horizontal genes transfer. Surprisingly,smu_1361cfunctions as a transcriptional repressor to regulate gene expression outside its operon, involved in the oxidative stress response ofS. mutans. Thesmu_1361coverexpression strain UA159/pDL278-1361cwas more susceptible to oxidative stress and less competitive against hydrogen peroxide generated by commensal speciesStreptococcus gordoniiandStreptococcus sanguinis. Transcriptomics analysis revealed thatsmu_1361coverexpression resulted in the significant downregulation of 22 genes mainly belonging to three gene clusters responsible for the oxidative stress response. The conversed DNA binding motif of SMU_1361c was determined by electrophoretic mobility shift and DNase I footprinting assay with purified SMU_1361c protein, therefore,smu_1361cis directly involved in gene transcription related to the oxidative stress response. Crucially, our finding provides a new understanding of howS. mutansdeals with the oxidative stress that is required for pathogenesis and will facilitate the development of new and improved therapeutic approaches for dental caries.