Morphological and physiological changes induced by contact-dependent interaction between Candida albicans and Fusobacterium nucleatum

Sci Rep. 2016 Jun 14:6:27956. doi: 10.1038/srep27956.

Abstract

Candida albicans and Fusobacterium nucleatum are well-studied oral commensal microbes with pathogenic potential that are involved in various oral polymicrobial infectious diseases. Recently, we demonstrated that F. nucleatum ATCC 23726 coaggregates with C. albicans SN152, a process mainly mediated by fusobacterial membrane protein RadD and Candida cell wall protein Flo9. The aim of this study was to investigate the potential biological impact of this inter-kingdom interaction. We found that F. nucleatum ATCC 23726 inhibits growth and hyphal morphogenesis of C. albicans SN152 in a contact-dependent manner. Further analysis revealed that the inhibition of Candida hyphal morphogenesis is mediated via RadD and Flo9 protein pair. Using a murine macrophage cell line, we showed that the F. nucleatum-induced inhibition of Candida hyphal morphogenesis promotes C. albicans survival and negatively impacts the macrophage-killing capability of C. albicans. Furthermore, the yeast form of C. albicans repressed F. nucleatum-induced MCP-1 and TNFα production in macrophages. Our study suggests that the interaction between C. albicans and F. nucleatum leads to a mutual attenuation of virulence, which may function to promote a long-term commensal lifestyle within the oral cavity. This finding has significant implications for our understanding of inter-kingdom interaction and may impact clinical treatment strategies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Candida albicans / genetics
  • Candida albicans / immunology*
  • Candida albicans / metabolism*
  • Cell Aggregation / physiology*
  • Cell Line
  • Chemokine CCL2 / biosynthesis
  • Coculture Techniques
  • Fusobacterium nucleatum / metabolism*
  • Hyphae / cytology
  • Hyphae / genetics
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Mice
  • Microbial Interactions / physiology*
  • Microbiota / physiology
  • Mouth / microbiology
  • Symbiosis / physiology
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Tumor Necrosis Factor-alpha