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Understanding the Streptococcus mutans Cid/Lrg System through CidB Function
Author(s) -
SangJoon Ahn,
Kelly C. Rice
Publication year - 2016
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.01499-16
Subject(s) - biology , streptococcus mutans , ccpa , virulence , crispr , operon , biofilm , mutant , regulation of gene expression , phenotype , gene expression , genetics , gene , microbiology and biotechnology , bacteria , catabolite repression
TheStreptococcus mutans lrgAB andcidAB operons have been previously described as a potential model system to dissect the complexity of biofilm development and virulence ofS. mutans . Herein, we have attempted to further characterize the Cid/Lrg system by focusing on CidB, which has been shown to be critical for the ability ofS. mutans to survive and persist in a nonpreferred oxygen-enriched condition. We have found that the expression level ofcidB is critical to oxidative stress tolerance ofS. mutans , most likely by impactinglrg expression. Intriguingly, the impaired aerobic growth phenotype of thecidB mutant could be restored by the additional loss of either CidA or LrgA. Growth-dependent expression ofcid andlrg was demonstrated to be tightly under the control of both CcpA and the VicKR two-component system (TCS), regulators known to play an essential role in controlling major catabolic pathways and cell envelope homeostasis, respectively. RNA sequencing (RNA-Seq) analysis revealed that mutation ofcidB resulted in global gene expression changes, comprising major domains of central metabolism and virulence processes, particularly in those involved with oxidative stress resistance. Loss of CidB also significantly changed the expression of genes related to genomic islands (GI) TnSmu1 and TnSmu2, the CRISPR (clustered regularly interspaced short palindromic repeats)-Cas system, and toxin-antitoxin (T/A) modules. Taken together, these data show that CidB impinges on the stress response, as well as the fundamental cellular physiology ofS. mutans , and further suggest a potential link between Cid/Lrg-mediated cellular processes,S. mutans pathogenicity, and possible programmed growth arrest and cell death mechanisms.IMPORTANCE The ability ofStreptococcus mutans to survive a variety of harmful or stressful conditions and to emerge as a numerically significant member of stable oral biofilm communities are essential elements for its persistence and cariogenicity. In this study, the homologouscidAB andlrgAB operons, previously identified as being highly balanced and coordinated duringS. mutans aerobic growth, were further characterized through the functional and transcriptomic analysis of CidB. Precise control of CidB levels is shown to impact the expression oflrg , oxidative stress tolerance, major metabolic domains, and the molecular modules linked to cell death and lysis. This study advances our understanding of the Cid/Lrg system as a key player in the integration of complex environmental signals (such as oxidative stress) into the regulatory networks that modulateS. mutans virulence and cell homeostasis.

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