| Literature DB >> 34637779 |
Otari Chipashvili1, Daniel R Utter2, Joseph K Bedree3, Yansong Ma1, Fabian Schulte4, Gabrielle Mascarin1, Yasmin Alayyoubi1, Deepak Chouhan5, Markus Hardt4, Felicitas Bidlack4, Hatice Hasturk1, Xuesong He5, Jeffrey S McLean6, Batbileg Bor7.
Abstract
Saccharibacteria (TM7) are obligate epibionts living on the surface of their host bacteria and are strongly correlated with dysbiotic microbiomes during periodontitis and other inflammatory diseases, suggesting they are putative pathogens. However, due to the recalcitrance of TM7 cultivation, causal research to investigate their role in inflammatory diseases is lacking. Here, we isolated multiple TM7 species on their host bacteria from periodontitis patients. These TM7 species reduce inflammation and consequential bone loss by modulating host bacterial pathogenicity in a mouse ligature-induced periodontitis model. Two host bacterial functions involved in collagen binding and utilization of eukaryotic sialic acid are required for inducing bone loss and are altered by TM7 association. This TM7-mediated downregulation of host bacterial pathogenicity is shown for multiple TM7/host bacteria pairs, suggesting that, in contrast to their suspected pathogenic role, TM7 could protect mammalian hosts from inflammatory damage induced by their host bacteria.Entities:
Keywords: Actinobacteria; Actinomyces; Saccharibacteria; TM7; bacterial symbiosis; candidate phyla radiation; human microbiome; human oral microbiome; inflammatory disease; periodontitis
Mesh:
Substances:
Year: 2021 PMID: 34637779 PMCID: PMC8595704 DOI: 10.1016/j.chom.2021.09.009
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023