<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He J</submitter><funding>NIDCR NIH HHS</funding><pagination>1036</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5462986</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>Early childhood caries (ECC), which can lead to rampant tooth-decay that is painful and costly to treat, is one of the most prevalent infectious diseases affecting children worldwide. Previous studies support that interactions between &lt;i>Streptococcus mutans&lt;/i> and &lt;i>Candida albicans&lt;/i> are associated with the pathogenesis of ECC. The presence of &lt;i>Candida&lt;/i> enhances &lt;i>S. mutans&lt;/i> growth, fitness and accumulation within biofilms &lt;i>in vitro&lt;/i>, although the molecular basis for these behaviors is undefined. Using an established co-cultivation biofilm model and RNA-Seq, we investigated how &lt;i>C. albicans&lt;/i> influences the transcriptome of &lt;i>S. mutans&lt;/i>. The presence of &lt;i>C. albicans&lt;/i> dramatically altered gene expression in &lt;i>S. mutans&lt;/i> in the dual-species biofilm, resulting in 393 genes differentially expressed, compared to mono-species biofilms of &lt;i>S. mutans&lt;/i>. By Gene Ontology analysis, the majority of up-regulated genes were related to carbohydrate transport and metabolic/catabolic processes. KEGG pathway impact analysis showed elevated pyruvate and galactose metabolism, suggesting that co-cultivation with &lt;i>C. albicans&lt;/i> influences carbohydrate utilization by &lt;i>S. mutans&lt;/i>. Analysis of metabolites confirmed the increases in carbohydrate metabolism, with elevated amounts of formate in the culture medium of co-cultured biofilms. Moreover, co-cultivation with &lt;i>C. albicans&lt;/i> altered transcription of &lt;i>S. mutans&lt;/i> signal transduction (&lt;i>comC&lt;/i> and &lt;i>ciaRH&lt;/i>) genes associated with fitness and virulence. Interestingly, the expression of genes for mutacins (bacteriocins) and CRISPR were down-regulated. Collectively, the data provide a comprehensive insight into &lt;i>S. mutans&lt;/i> transcriptomic changes induced by &lt;i>C. albicans&lt;/i>, and offer novel insights into how bacterial-fungal interactions may enhance the severity of dental caries.</pubmed_abstract><journal>Frontiers in microbiology</journal><pubmed_title>RNA-Seq Reveals Enhanced Sugar Metabolism in &lt;i>Streptococcus mutans&lt;/i> Co-cultured with &lt;i>Candida albicans&lt;/i> within Mixed-Species Biofilms.</pubmed_title><pmcid>PMC5462986</pmcid><funding_grant_id>R01 DE018023</funding_grant_id><funding_grant_id>R01 DE025220</funding_grant_id><pubmed_authors>Kim D</pubmed_authors><pubmed_authors>Burne RA</pubmed_authors><pubmed_authors>Richards VP</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Ahn SJ</pubmed_authors><pubmed_authors>Koo H</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-Seq Reveals Enhanced Sugar Metabolism in &lt;i>Streptococcus mutans&lt;/i> Co-cultured with &lt;i>Candida albicans&lt;/i> within Mixed-Species Biofilms.</name><description>Early childhood caries (ECC), which can lead to rampant tooth-decay that is painful and costly to treat, is one of the most prevalent infectious diseases affecting children worldwide. Previous studies support that interactions between &lt;i>Streptococcus mutans&lt;/i> and &lt;i>Candida albicans&lt;/i> are associated with the pathogenesis of ECC. The presence of &lt;i>Candida&lt;/i> enhances &lt;i>S. mutans&lt;/i> growth, fitness and accumulation within biofilms &lt;i>in vitro&lt;/i>, although the molecular basis for these behaviors is undefined. Using an established co-cultivation biofilm model and RNA-Seq, we investigated how &lt;i>C. albicans&lt;/i> influences the transcriptome of &lt;i>S. mutans&lt;/i>. The presence of &lt;i>C. albicans&lt;/i> dramatically altered gene expression in &lt;i>S. mutans&lt;/i> in the dual-species biofilm, resulting in 393 genes differentially expressed, compared to mono-species biofilms of &lt;i>S. mutans&lt;/i>. By Gene Ontology analysis, the majority of up-regulated genes were related to carbohydrate transport and metabolic/catabolic processes. KEGG pathway impact analysis showed elevated pyruvate and galactose metabolism, suggesting that co-cultivation with &lt;i>C. albicans&lt;/i> influences carbohydrate utilization by &lt;i>S. mutans&lt;/i>. Analysis of metabolites confirmed the increases in carbohydrate metabolism, with elevated amounts of formate in the culture medium of co-cultured biofilms. Moreover, co-cultivation with &lt;i>C. albicans&lt;/i> altered transcription of &lt;i>S. mutans&lt;/i> signal transduction (&lt;i>comC&lt;/i> and &lt;i>ciaRH&lt;/i>) genes associated with fitness and virulence. Interestingly, the expression of genes for mutacins (bacteriocins) and CRISPR were down-regulated. Collectively, the data provide a comprehensive insight into &lt;i>S. mutans&lt;/i> transcriptomic changes induced by &lt;i>C. albicans&lt;/i>, and offer novel insights into how bacterial-fungal interactions may enhance the severity of dental caries.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2026-05-04T21:02:01.271Z</modification><creation>2019-03-27T02:47:06Z</creation></dates><accession>S-EPMC5462986</accession><cross_references><pubmed>28642749</pubmed><doi>10.3389/fmicb.2017.01036</doi></cross_references></HashMap>