Diarrheal-associated gut dysbiosis in cancer and inflammatory bowel disease patients is exacerbated by Clostridioides difficile infection
Dysbiosis
Faecalibacterium prausnitzii
DOI:
10.3389/fcimb.2023.1190910
Publication Date:
2023-07-27T15:40:35Z
AUTHORS (12)
ABSTRACT
Introduction Low diversity gut dysbiosis can take different forms depending on the disease context. In this study, we used shotgun metagenomic sequencing and gas chromatography–mass spectrometry (GC-MS) to compared metabolomic profiles of Clostridioides (Clostridium) difficile diarrheal cancer inflammatory bowel (IBD) patients defined additive effect C. infection (CDI) intestinal dysbiosis. Results The study cohort consisted 138 case-mix patients, 43 IBD 45 healthy control individuals. Thirty-three were also infected with . group, three well-known enterotypes identified, while other groups presented an additional Escherichia -driven enterotype. Bacterial was significantly lower in all than controls, highest level bacterial species richness observed patients. Fifty-six had abundance levels that differentiated patient from group. Of these species, 52 4 ( Bacteroides fragilis , coli Klebsiella pneumoniae Ruminococcus gnavus ) under-represented over-represented, respectively, groups. relative abundances propionate butyrate fecal samples CDI samples. Isobutyrate, propanate, concentrations cancer, IBD, samples, respectively. Glycine valine amino acids over- represented Conclusion Our data indicate external internal factors drive comparable low While diarrheal-related may be a consequence systemic therapy, similar phenotype is cases moderate severe both cases, exacerbated by incidence CDI.
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