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

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 tha...

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Autores principales: Ricci, Liviana, Mackie, Joanna, Donachie, Gillian E, Chapuis, Ambre, Mezerová, Kristýna, Lenardon, Megan D, Brown, Alistair J P, Duncan, Sylvia H, Walker, Alan W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486989/
https://www.ncbi.nlm.nih.gov/pubmed/36007932
http://dx.doi.org/10.1093/femsec/fiac095
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author Ricci, Liviana
Mackie, Joanna
Donachie, Gillian E
Chapuis, Ambre
Mezerová, Kristýna
Lenardon, Megan D
Brown, Alistair J P
Duncan, Sylvia H
Walker, Alan W
author_facet Ricci, Liviana
Mackie, Joanna
Donachie, Gillian E
Chapuis, Ambre
Mezerová, Kristýna
Lenardon, Megan D
Brown, Alistair J P
Duncan, Sylvia H
Walker, Alan W
author_sort Ricci, Liviana
collection PubMed
description 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.
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spelling pubmed-94869892022-09-20 Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans Ricci, Liviana Mackie, Joanna Donachie, Gillian E Chapuis, Ambre Mezerová, Kristýna Lenardon, Megan D Brown, Alistair J P Duncan, Sylvia H Walker, Alan W FEMS Microbiol Ecol Research Article 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. Oxford University Press 2022-08-25 /pmc/articles/PMC9486989/ /pubmed/36007932 http://dx.doi.org/10.1093/femsec/fiac095 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ricci, Liviana
Mackie, Joanna
Donachie, Gillian E
Chapuis, Ambre
Mezerová, Kristýna
Lenardon, Megan D
Brown, Alistair J P
Duncan, Sylvia H
Walker, Alan W
Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title_full Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title_fullStr Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title_full_unstemmed Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title_short Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
title_sort human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen candida albicans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486989/
https://www.ncbi.nlm.nih.gov/pubmed/36007932
http://dx.doi.org/10.1093/femsec/fiac095
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