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In this study, we identified a two-component system,\n            <jats:named-content content-type=\"genus-species\">S. sanguinis<\/jats:named-content>\n            SptRS (SptRS\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            ), affecting\n            <jats:named-content content-type=\"genus-species\">S. sanguinis<\/jats:named-content>\n            survival in saliva and biofilm formation. Isogenic mutants of\n            <jats:italic>\n              sptR\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            (SKsptR) and\n            <jats:italic>\n              sptS\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            (SKsptS) showed reduced cell counts in\n            <jats:italic>ex vivo<\/jats:italic>\n            assays of viability in saliva compared to those of parent strain SK36 and complemented mutants. Reduced counts of the mutants in saliva were associated with reduced growth rates in nutrient-poor medium (RPMI) and increased susceptibility to the deposition of C3b and the membrane attach complex (MAC) of the complement system, a defense component of saliva and serum. Conversely,\n            <jats:italic>\n              sptR\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            and\n            <jats:italic>\n              sptS\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            mutants showed increased biofilm formation associated with higher levels of production of H\n            <jats:sub>2<\/jats:sub>\n            O\n            <jats:sub>2<\/jats:sub>\n            and extracellular DNA. Reverse transcription-quantitative PCR (RT-qPCR) comparisons of strains indicated a global role of SptRS\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            in repressing genes for H\n            <jats:sub>2<\/jats:sub>\n            O\n            <jats:sub>2<\/jats:sub>\n            production (2.5- to 15-fold upregulation of\n            <jats:italic>spxB<\/jats:italic>\n            ,\n            <jats:italic>spxR<\/jats:italic>\n            ,\n            <jats:italic>vicR<\/jats:italic>\n            ,\n            <jats:italic>tpk<\/jats:italic>\n            , and\n            <jats:italic>ackA<\/jats:italic>\n            in\n            <jats:italic>\n              sptR\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            and\n            <jats:italic>\n              sptS\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            mutants), biofilm formation, and\/or evasion of host immunity (2.1- to 11.4-fold upregulation of\n            <jats:italic>srtA<\/jats:italic>\n            ,\n            <jats:italic>pcsB<\/jats:italic>\n            ,\n            <jats:italic>cwdP<\/jats:italic>\n            ,\n            <jats:italic>iga<\/jats:italic>\n            , and\n            <jats:italic>nt5e<\/jats:italic>\n            ). Compatible with the homology of SptR\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            with AraC-type regulators, duplicate to multiple conserved repeats were identified in 1,000-bp regulatory regions of downstream genes, suggesting that SptR\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            regulates transcription by DNA looping. Significant transcriptional changes in the regulatory genes\n            <jats:italic>vicR<\/jats:italic>\n            ,\n            <jats:italic>spxR<\/jats:italic>\n            ,\n            <jats:italic>comE<\/jats:italic>\n            ,\n            <jats:italic>comX<\/jats:italic>\n            , and\n            <jats:italic>mecA<\/jats:italic>\n            in the\n            <jats:italic>\n              sptR\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            and\n            <jats:italic>\n              sptS\n              <jats:sub>Ss<\/jats:sub>\n            <\/jats:italic>\n            mutants further indicated that SptRS\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            is part of a regulatory network that coordinates cell wall homeostasis, H\n            <jats:sub>2<\/jats:sub>\n            O\n            <jats:sub>2<\/jats:sub>\n            production, and competence. This study reveals that SptRS\n            <jats:sub>\n              <jats:italic>Ss<\/jats:italic>\n            <\/jats:sub>\n            is involved in the regulation of crucial functions for\n            <jats:named-content content-type=\"genus-species\">S. sanguinis<\/jats:named-content>\n            persistence in the oral cavity.\n          <\/jats:p>","DOI":"10.1128\/iai.00942-17","type":"journal-article","created":{"date-parts":[[2018,1,11]],"date-time":"2018-01-11T10:59:40Z","timestamp":1515668380000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":21,"title":["Novel Two-Component System of Streptococcus sanguinis Affecting Functions Associated with Viability in Saliva and Biofilm Formation"],"prefix":"10.1128","volume":"86","author":[{"given":"Tarsila M.","family":"Camargo","sequence":"first","affiliation":[{"name":"Department of Oral Diagnosis, Piracicaba Dental School, University of Campinas-UNICAMP, SP, 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