<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hoare A</submitter><funding>NIDCR NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Dental and Craniofacial Research</funding><funding>FONDECYT</funding><pagination>1490-1504</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8115154</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(5)</volume><pubmed_abstract>Recent studies describe in detail the shifts in composition of human-associated polymicrobial communities from health to disease. However, the specific processes that drive the colonization and overgrowth of pathogens within these communities remain incompletely understood. We used in vitro culture systems and a disease-relevant mouse model to show that population size, which determines the availability of an endogenous diffusible small molecule, limits the growth, colonization, and in vivo virulence of the human oral pathogen Porphyromonas gingivalis. This bacterial pathogen overcomes the requirement for an endogenous cue by utilizing a cell-density dependent, growth-promoting, soluble molecule provided by the symbiotic early colonizer Veillonella parvula, but not produced by other commen</pubmed_abstract><journal>The ISME journal</journal><pubmed_title>A cross-species interaction with a symbiotic commensal enables cell-density-dependent growth and in vivo virulence of an oral pathogen.</pubmed_title><pmcid>PMC8115154</pmcid><funding_grant_id>R01DE015254</funding_grant_id><funding_grant_id>R21 DE023967</funding_grant_id><funding_grant_id>R01 DE015254</funding_grant_id><pubmed_authors>Abusleme L</pubmed_authors><pubmed_authors>Marsh PD</pubmed_authors><pubmed_authors>Hoare A</pubmed_authors><pubmed_authors>Diaz PI</pubmed_authors><pubmed_authors>Hajishengallis G</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Meethil A</pubmed_authors><pubmed_authors>Hong BY</pubmed_authors><pubmed_authors>Moutsopoulos NM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A cross-species interaction with a symbiotic commensal enables cell-density-dependent growth and in vivo virulence of an oral pathogen.</name><description>Recent studies describe in detail the shifts in composition of human-associated polymicrobial communities from health to disease. However, the specific processes that drive the colonization and overgrowth of pathogens within these communities remain incompletely understood. We used in vitro culture systems and a disease-relevant mouse model to show that population size, which determines the availability of an endogenous diffusible small molecule, limits the growth, colonization, and in vivo virulence of the human oral pathogen Porphyromonas gingivalis. This bacterial pathogen overcomes the requirement for an endogenous cue by utilizing a cell-density dependent, growth-promoting, soluble molecule provided by the symbiotic early colonizer Veillonella parvula, but not produced by other commen</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-04-04T10:17:54.77Z</modification><creation>2025-04-04T10:17:54.77Z</creation></dates><accession>S-EPMC8115154</accession><cross_references><pubmed>33372193</pubmed><doi>10.1038/s41396-020-00865-y</doi></cross_references></HashMap>