Abstract

The oral cavity is a complex environment harboring diverse microbial species that often co-exist within biofilms formed on oral surfaces. Within a biofilm, inter-species interactions can be synergistic in that the presence of one organism generates a niche for another enhancing colonization. Among these species are the opportunistic fungal pathogen Candida albicans and the bacterial species Streptococcus mutans, the etiologic agents of oral candidiasis and dental caries, respectively. Recent studies have reported enhanced prevalence of C. albicans in children with caries indicating potential clinical implications for this fungal-bacterial interaction. In this study, we aimed to specifically elucidate the role of C. albicans-derived polysaccharide biofilm matrix components in augmenting S. mutans colonization and mixed biofilm formation. Comparative evaluations of single and mixed species biofilms demonstrated significantly enhanced S. mutans retention in mixed biofilms with C. albicans. Further, S. mutans single species biofilms were enhanced upon exogenous supplementation with purified matrix material derived from C. albicans biofilms. Similarly, growth in C. albicans cell-free spent biofilm culture media enhanced S. mutans single species biofilm formation, however, the observed increase in S. mutans biofilms was significantly affected upon enzymatic digestion of polysaccharides in spent media, identifying C. albicans secreted polysaccharides as a key factor in mediating mixed biofilm formation. The enhanced S. mutans biofilms mediated by the various C. albicans effectors was also demonstrated using confocal laser scanning microscopy. Importantly, a clinically relevant mouse model of oral co-infection was adapted to demonstrate the C. albicans-mediated enhanced S. mutans colonization in a host. Analyses of harvested tissue and scanning electron microscopy demonstrated significantly higher S. mutans retention on teeth and tongues of co-infected mice compared to mice infected only with S. mutans. Collectively, the findings from this study strongly indicate that the secretion of polysacharides from C. albicans in the oral environment may impact the development of S. mutans biofilms, ultimately increasing dental caries and, therefore, Candida oral colonization should be considered as a factor in evaluating the risk of caries.

Highlights

  • The oral microbiome is one of the most complex environments harboring diverse microbiota that co-exist in equilibrium (Wade, 2013; Krom et al, 2014; Xu and Dongari-Bagtzoglou, 2015; Sultan et al, 2018)

  • S. mutans recovery from single and mixed-species biofilms was comparatively assessed based on colony-forming units (CFU) counts; results demonstrated significantly enhanced S. mutans recovery from mixed biofilms with C. albicans compared to S. mutans singlespecies biofilms

  • Confocal Laser Scaning Microscopy (CLSM) analysis of formed biofilms revealed that, compared to S. mutans single biofilm, growth with C. albicans resulted in a significant increase in biofilm biomass and complexity concurrent with a significantly increased level of S. mutans retention (Figures 2B,D,F)

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Summary

Introduction

The oral microbiome is one of the most complex environments harboring diverse microbiota that co-exist in equilibrium (Wade, 2013; Krom et al, 2014; Xu and Dongari-Bagtzoglou, 2015; Sultan et al, 2018). Microorganisms exist within highly organized and structured microbial communities referred to as biofilms, where microbial cells are embedded within a self-produced extracellular polymeric substance (Jenkinson et al, 1990; Kolenbrander et al, 2002; Rickard et al, 2003; Vu et al, 2009) In this environment, extensive inter-species interactions take place, which can be synergistic in that the presence of one organism generates a niche for others, enhancing colonization and retention (Xiao et al, 2012; Sultan et al, 2018). S. mutans has long been considered the main cariogenic species, recent evidence seems to attribute a potential role for the fungal species Candida albicans, via interactions with S. mutans (Metwalli et al, 2013; Falsetta et al, 2014; Pereira et al, 2018; Xiao et al, 2018)

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