Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans

Author:

Ricci Liviana12,Mackie Joanna3,Donachie Gillian E1,Chapuis Ambre3,Mezerová Kristýna4,Lenardon Megan D35ORCID,Brown Alistair J P36ORCID,Duncan Sylvia H1ORCID,Walker Alan W1ORCID

Affiliation:

1. Rowett Institute, University of Aberdeen , Aberdeen, AB25 2ZD, United Kingdom

2. CIBIO - Department of Cellular, Computational and Integrative Biology, University of Trento , Trento, 38123, Italy

3. Aberdeen Fungal Group, Institute of Medical Sciences, University of Aberdeen , Aberdeen, AB25 2ZD, United Kingdom

4. Department of Microbiology, Faculty of Medicine and Dentistry, Palacký University Olomouc , Olomouc, 77515, Czech Republic

5. School of Biotechnology and Biomolecular Sciences, University of New South Wales , Sydney, NSW 2052, Australia

6. MRC Centre for Medical Mycology, University of Exeter , Exeter, EX4 4QD, United Kingdom

Abstract

Abstract The human gut microbiota protects the host from invading pathogens and the overgrowth of indigenous opportunistic species via a process called colonization resistance. Here, we investigated the antagonistic activity of human gut bacteria towards Candida albicans, an opportunistic fungal pathogen that can cause severe infections in susceptible individuals. Coculture batch incubations of C. albicans in the presence of faecal microbiota from six healthy individuals revealed varying levels of inhibitory activity against C. albicans. 16S rRNA gene amplicon profiling of these faecal coculture bacterial communities showed that the Bifidobacteriaceae family, and Bifidobacterium adolescentis in particular, were most correlated with antagonistic activity against C. albicans. Follow-up mechanistic studies performed under anaerobic conditions confirmed that culture supernatants of Bifidobacterium species, particularly B. adolescentis, inhibited C. albicans in vitro. Fermentation acids (FA), including acetate and lactate, present in the bifidobacterial supernatants were important contributors to inhibitory activity. However, increasing the pH of both bacterial supernatants and mixtures of FA reduced their anti-Candida effects, indicating a combinatorial effect of prevailing pH and FA. This work, therefore, demonstrates potential mechanisms underpinning gut microbiome-mediated colonization resistance against C. albicans, and identifies particularly inhibitory components such as bifidobacteria and FA as targets for further study.

Funder

Wellcome

Rural and Environment Science and Analytical Services Division

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Ecology,Microbiology

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