Back to Search
Start Over
Candida tropicalis Infection Modulates the Gut Microbiome and Confers Enhanced Susceptibility to Colitis in Mice
- Source :
- Cellular and Molecular Gastroenterology and Hepatology, Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 3, Pp 901-923 (2022)
- Publication Year :
- 2021
-
Abstract
- Background & Aims We previously showed that abundance of Candida tropicalis is significantly greater in Crohn’s disease patients compared with first-degree relatives without Crohn’s disease. The aim of this study was to determine the effects and mechanisms of action of C tropicalis infection on intestinal inflammation and injury in mice. Methods C57BL/6 mice were inoculated with C tropicalis, and colitis was induced by administration of dextran sodium sulfate in drinking water. Disease severity and intestinal permeability subsequently were evaluated by endoscopy, histology, quantitative reverse-transcription polymerase chain reaction, as well as 16S ribosomal RNA and NanoString analyses (NanoString Technologies, Seattle, WA). Results Infected mice showed more severe colitis, with alterations in gut mucosal helper T cells (Th)1 and Th17 cytokine expression, and an increased frequency of mesenteric lymph node–derived group 2 innate lymphoid cells compared with uninfected controls. Gut microbiome composition, including changes in the mucin-degrading bacteria, Akkermansia muciniphila and Ruminococcus gnavus, was altered significantly, as was expression of several genes affecting intestinal epithelial homeostasis in isolated colonoids, after C tropicalis infection compared with uninfected controls. In line with these findings, fecal microbiome transplantation of germ-free recipient mice using infected vs uninfected donors showed altered expression of several tight-junction proteins and increased susceptibility to dextran sodium sulfate–induced colitis. Conclusions C tropicalis induces dysbiosis that involves changes in the presence of mucin-degrading bacteria, leading to altered tight junction protein expression with increased intestinal permeability and followed by induction of robust Th1/Th17 responses, which ultimately lead to an accelerated proinflammatory phenotype in experimental colitic mice.<br />Graphical abstract
- Subjects :
- C tropicalis
A muciniphila
PBS, phosphate-buffered saline
RC799-869
Th, helper T cell
CARD9, caspase-associated recruitment domain adaptor 9
Mice
RT, reverse-transcription
Cldn, claudin
MLN, mesenteric lymph node
CD, Crohn’s disease
Animals
Humans
IFN, interferon
Candida tropicalis
Lymphocytes
DSS, dextran sodium sulfate
RFU, relative fluorescence unit
CWRU, Case Western Reserve University
Original Research
T-bet+, _
TNF, tumor necrosis factor
Hepatology
IBD, inflammatory bowel disease
FMT, fecal microbiome transplantation
RORγT+, __
Dextran Sulfate
Gastroenterology
ILC, innate lymphoid cell
Diseases of the digestive system. Gastroenterology
Colitis
Immunity, Innate
B6, C57BL/6
CFU, colony forming unit
Gastrointestinal Microbiome
IL, interleukin
Mice, Inbred C57BL
rRNA, ribosomal RNA
GF, germ-free
UC, ulcerative colitis
IEBD, intestinal epithelial barrier dysfunction
qPCR, quantitative polymerase chain reaction
FITC, fluorescein isothiocyanate
Mycobiome
Subjects
Details
- ISSN :
- 2352345X
- Volume :
- 13
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Cellular and molecular gastroenterology and hepatology
- Accession number :
- edsair.doi.dedup.....79c626a9a297f966395077b58c0ab96c