Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola. Issue 1 (1st January 2020)

• Record Type: Journal Article
• Authors: Kin, Lin Xin; Butler, Catherine A.; Slakeski, Nada; Hoffmann, Brigitte; Dashper, Stuart G.; Reynolds, Eric C.
• Is Part Of: Journal of oral microbiology. Volume 12:Issue 1(2020)
• Publication Date: 2020-01-01
• Subjects: Chronic periodontitis -- Porphyromonas gingivalis -- Treponema denticola -- polymicrobial community -- dysbiosis -- metabolic cooperativity; Mouth -- Microbiology -- Periodicals; Medical microbiology -- Periodicals; Mouth Diseases -- microbiology; Mouth -- microbiology; Medical microbiology; Mouth -- Microbiology; Oral Pathology; Microbiology; Periodicals; Periodicals; Fulltext; Internet Resources; Periodicals; Electronic journals; 616.31
• DOI: 10.1080/20002297.2020.1808750
• Languages: English
• ISSNs: 2000-2297

Abstract

ABSTRACT: Background: Porphyromonas gingivalis and Treponema denticola are proteolytic periodontopathogens that co-localize in polymicrobial subgingival plaque biofilms, display in vitro growth symbiosis and synergistic virulence in animal models of disease. These symbioses are underpinned by a range of metabolic interactions including cooperative hydrolysis of glycine-containing peptides to produce free glycine, which T. denticola uses as a major energy and carbon source. Objective: To characterize the P. gingivalis gene products essential for these interactions. Methods: The P. gingivalis transcriptome exposed to cell-free T. denticola conditioned medium was determined using RNA-seq. P. gingivalis proteases potentially involved in hydrolysis of glycine-containing peptides were identified using a bioinformatics approach. Results: One hundred and thirty-twogenes displayed differential expression, with the pattern of gene expression consistent with succinate cross-feeding from T. denticola to P. gingivalis and metabolic shifts in the P. gingivalis folate-mediated one carbon superpathway. Interestingly, no P. gingivalis proteases were significantly up-regulated. Three P. gingivalis proteases were identified as candidates and inactivated to determine their role in the release of free glycine. P. gingivalis PG0753 and PG1788 but not PG1605 are involved in the hydrolysis of glycine-containing peptides, making free glycine available for T. denticola utilization. Conclusion: Collectively these metabolic interactions help to partition resources and engage synergistic interactions between these two species.