Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 290, Issue 35, Pages 21185-21198Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M115.644401
Keywords
biofilm; cell metabolism; metabolic regulation; metabolomics; Streptococcus; symbiosis; Fusobacterium; arginine metabolism; cross-feeding; ornithine export
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Funding
- CREST from Japan Science and Technology Agency
- Japan Society for the Promotion of Science [262530940, 245931500]
- Osaka University Graduate School of Dentistry
- Grants-in-Aid for Scientific Research [15K20360, 26253094, 15K20642, 15J05275] Funding Source: KAKEN
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Background: Arginine and its derivatives are key factors for inter-bacterial communication in periodontal microflora. Results: ArcD-mediated export of ornithine by oral commensal Streptococcus gordonii facilitates biofilm development of Fusobacterium nucleatum. Conclusion: Ornithine cross-feeding from S. gordonii to F. nucleatum mediates dental biofilm maturation. Significance: This is the first report of metabolic cross-feeding between S. gordonii and F. nucleatum. Arginine is utilized by the oral inhabitant Streptococcus gordonii as a substrate of the arginine deiminase system (ADS), eventually producing ATP and NH3, the latter of which is responsible for microbial resistance to pH stress. S. gordonii expresses a putative arginine-ornithine antiporter (ArcD) whose function has not been investigated despite relevance to the ADS and potential influence on inter-bacterial communication with periodontal pathogens that utilize amino acids as a main energy source. Here, we generated an S. gordonii arcD mutant to explore the role of ArcD in physiological homeostasis and bacterial cross-feeding. First, we confirmed that S. gordonii ArcD plays crucial roles for mediating arginine uptake and promoting bacterial growth, particularly under arginine-limited conditions. Next, metabolomic profiling and transcriptional analysis of the arcD mutant revealed that deletion of this gene caused intracellular accumulation of ornithine leading to malfunction of the ADS and suppression of de novo arginine biosynthesis. The mutant strain also showed increased susceptibility to low pH stress due to reduced production of ammonia. Finally, accumulation of Fusobacterium nucleatum was found to be significantly decreased in biofilm formed by the arcD mutant as compared with the wild-type strain, although ornithine supplementation restored fusobacterium biovolume in dual-species biofilms with the arcD mutant and also enhanced single species biofilm development by F. nucleatum. Our results are the first direct evidence showing that S. gordonii ArcD modulates not only alkali and energy production but also interspecies interaction with F. nucleatum, thus initiating a middle stage of periodontopathic biofilm formation, by metabolic cross-feeding.
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