Oral Candida administration in a Clostridium difficile mouse model worsens disease severity but is attenuated by Bifidobacterium.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 04 07 2018
accepted: 02 01 2019
entrez: 16 1 2019
pubmed: 16 1 2019
medline: 2 11 2019
Statut: epublish

Résumé

Gut fungi may influence the course of Clostridium difficile infection either positively or negatively for the host. Fungi are not prominent in the mouse gut, and C. albicans, the major human gastrointestinal commensal yeast, is in low abundance or absent in mice. Bifidobacterium is one of the probiotics that may attenuate the severity of C. difficile infection. Inflammatory synergy between C. albicans and C. difficile, in gut, may provide a state that more closely resembles human infection and be more suitable for testing probiotic effects. We performed fecal mycobiota analysis and administered C. albicans at 1 day prior to C. difficile dosing. Fecal eukaryotic 18S rDNA analysis demonstrated the presence of Ascomycota, specifically, Candida spp., after oral antibiotics, despite negative fecal fungal culture. C. albicans administration enhanced the severity of the C. difficile infection model as determined by mortality rate, weight loss, gut leakage (FITC-dextran assay), and serum and intestinal tissue cytokines. This occurred without increased fecal C. difficile or bacteremia, in comparison with C. difficile gavage alone. Candida lysate with C. difficile increased IL-8 production from HT-29 and Caco-2 human intestinal epithelial cell-lines. Bifidobacterium attenuated the disease severity of the C. difficile plus Candida model. The reduced severity was associated with decreased Candida burdens in feces. In conclusion, gut C. albicans worsened C. difficile infection, possibly through exacerbation of inflammation. Hence, a mouse model of Clostridium difficile infection with C. albicans present in the gut may better model the human patient condition. Gut fungal mycobiome investigation in patients with C. difficile is warranted and may suggest therapeutic targets.

Identifiants

pubmed: 30645630
doi: 10.1371/journal.pone.0210798
pii: PONE-D-18-19870
pmc: PMC6333342
doi:

Substances chimiques

CXCL8 protein, human 0
Interleukin-8 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0210798

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: MF received salary from Cape Cod Inc. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Wimonrat Panpetch (W)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Naraporn Somboonna (N)

Department of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.

Matanee Palasuk (M)

Department of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.

Pratsanee Hiengrach (P)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Malcolm Finkelman (M)

Associates of Cape Cod, Inc., East Falmouth, MA, USA.

Somying Tumwasorn (S)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Asada Leelahavanichkul (A)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Center of Excellence in Immunology and Immune-mediated Diseases, Department of Microbiology, Chulalongkorn University, Bangkok, Thailand.

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Classifications MeSH