Investigating the role of Candida albicans as a universal substrate for oral bacteria using a transcriptomic approach: implications for interkingdom biofilm control?

Author:

Delaney Christopher12,Alapati Susanth12,Alshehri Muhanna12,Kubalova Dominika12,Veena Chandra Lekha Ramalingham12,Abusrewil Sumaya12,Short Bryn12,Bradshaw David3,Brown Jason L.12

Affiliation:

1. Oral Sciences Research Group, Glasgow Dental School, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences University of Glasgow Glasgow UK

2. Glasgow Biofilm Research Network (www.glasgowbiofilms.ac.uk) Glasgow UK

3. R&D Innovation, Haleon Weybridge UK

Abstract

Candida albicans is frequently identified as a colonizer of the oral cavity in health and has recently been termed a “keystone” commensal due to its role on the bacterial communities. However, the role that C. albicans plays in such interactions is not fully understood. Therefore, this study aimed to identify the relationship between C. albicans and bacteria associated with oral symbiosis and dysbiosis. To do this, we evaluated the ability of C. albicans to support the growth of the aerobic commensal Streptococcus gordonii and the anaerobic pathogens Fusobacterium nucleatum and Porphyromonas gingivalis in the biofilm environment. RNA‐Sequencing with the Illumina platform was then utilized to identify C. albicans gene expression and functional pathways involved during such interactions in dual‐species and a 4‐species biofilm model. Results indicated that C. albicans was capable of supporting growth of all three bacteria, with a significant increase in colony counts of each bacteria in the dual‐species biofilm (p < 0.05). We identified specific functional enrichment of pathways in our 4‐species community as well as transcriptional profiles unique to the F. nucleatum and S. gordonii dual‐species biofilms, indicating a species‐specific effect on C. albicans. Candida‐related hemin acquisition and heat shock protein mediated processes were unique to the organism following co‐culture with anaerobic and aerobic bacteria, respectively, suggestive that such pathways may be feasible options for therapeutic targeting to interfere with these fungal‐bacterial interactions. Targeted antifungal therapy may be considered as an option for biofilm destabilization and treatment of complex communities. Moving forward, we propose that further studies must continue to investigate the role of this fungal organism in the context of the interkingdom nature of oral diseases.

Publisher

Wiley

Subject

Microbiology (medical),General Medicine,Immunology and Allergy,Pathology and Forensic Medicine

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