<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>59(4)</volume><submitter>Sujitha S</submitter><pubmed_abstract>The proportion of people suffering from cardiovascular diseases has risen by 34% in the last 15 years in India. Cardiomyopathy is among the many forms of CVD s present. Infection of heart muscles is the suspected etiological agent for the same. Oral pathogens gaining entry into the bloodstream are responsible for such infections. &lt;i>Streptococcus mutans&lt;/i> is an oral pathogen with implications in cardiovascular diseases. Previous studies have shown certain strains of &lt;i>S. mutans&lt;/i> are found predominantly within atherosclerotic plaques and extirpated valves. To decipher the genetic differences responsible for endothelial cell invasion, we have sequenced the genome of &lt;i>Streptococcus mutans&lt;/i> B14. Pan-genome analysis, search for adhesion proteins through a special algorithm, and protein-protein interactions search through HPIDB have been done. Pan-genome analysis of 187 whole genomes, assemblies revealed 6965 genes in total and 918 genes forming the core gene cluster. Adhesion to the endothelial cell is a critical virulence factor distinguishing virulent and non-virulent strains. Overall, 4% of the total proteins in &lt;i>S. mutans&lt;/i> B14 were categorized as adhesion proteins. Protein-protein interaction between putative adhesion proteins and Human extracellular matrix components was predicted, revealing novel interactions. A conserved gene catalyzing the synthesis of branched-chain amino acids in &lt;i>S. mutans&lt;/i> B14 shows possible interaction with isoforms of cathepsin protein of the ECM. This genome sequence analysis indicates towards other proteins in the &lt;i>S. mutans&lt;/i> genome, which might have a specific role to play in host cell interaction.</pubmed_abstract><journal>Indian journal of microbiology</journal><pagination>451-459</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6842392</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome Investigation of a Cariogenic Pathogen with Implications in Cardiovascular Diseases.</pubmed_title><pmcid>PMC6842392</pmcid><pubmed_authors>Sujitha S</pubmed_authors><pubmed_authors>Karthikeyan R</pubmed_authors><pubmed_authors>Rajendhran J</pubmed_authors><pubmed_authors>Sankarasubramanian J</pubmed_authors><pubmed_authors>Vishnu US</pubmed_authors><pubmed_authors>Gunasekaran P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome Investigation of a Cariogenic Pathogen with Implications in Cardiovascular Diseases.</name><description>The proportion of people suffering from cardiovascular diseases has risen by 34% in the last 15 years in India. Cardiomyopathy is among the many forms of CVD s present. Infection of heart muscles is the suspected etiological agent for the same. Oral pathogens gaining entry into the bloodstream are responsible for such infections. &lt;i>Streptococcus mutans&lt;/i> is an oral pathogen with implications in cardiovascular diseases. Previous studies have shown certain strains of &lt;i>S. mutans&lt;/i> are found predominantly within atherosclerotic plaques and extirpated valves. To decipher the genetic differences responsible for endothelial cell invasion, we have sequenced the genome of &lt;i>Streptococcus mutans&lt;/i> B14. Pan-genome analysis, search for adhesion proteins through a special algorithm, and protein-protein interactions search through HPIDB have been done. Pan-genome analysis of 187 whole genomes, assemblies revealed 6965 genes in total and 918 genes forming the core gene cluster. Adhesion to the endothelial cell is a critical virulence factor distinguishing virulent and non-virulent strains. Overall, 4% of the total proteins in &lt;i>S. mutans&lt;/i> B14 were categorized as adhesion proteins. Protein-protein interaction between putative adhesion proteins and Human extracellular matrix components was predicted, revealing novel interactions. A conserved gene catalyzing the synthesis of branched-chain amino acids in &lt;i>S. mutans&lt;/i> B14 shows possible interaction with isoforms of cathepsin protein of the ECM. This genome sequence analysis indicates towards other proteins in the &lt;i>S. mutans&lt;/i> genome, which might have a specific role to play in host cell interaction.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2026-05-03T20:31:31.556Z</modification><creation>2021-02-20T02:48:13Z</creation></dates><accession>S-EPMC6842392</accession><cross_references><pubmed>31762508</pubmed><doi>10.1007/s12088-019-00823-z</doi></cross_references></HashMap>