AI Article Synopsis

  • * In a study involving cynomolgus monkeys, FMT was found to reduce diarrhea symptoms and regulate inflammatory markers in the serum, enhancing gut bacterial diversity by decreasing harmful pathogens and promoting beneficial ones.
  • * FMT also enriched the metabolic functions of gut bacteria in treated monkeys, shifted the fungal composition, and showed correlations between gut Archaea and anti-inflammatory responses, indicating its promise for treating chronic diarrhea.

Article Abstract

Chronic diarrhea is associated with enteric dysbiosis and provokes the overuse of antibiotics. Fecal microbiota transplantation (FMT) is a promising therapy, but it shows discrepant clinical efficacy. Bacterial colonization in recipients has been studied, although little is known about the role of gut fungi and Archaea after FMT. In this study, we evaluated the efficacy of human-derived FMT on spontaneous chronic diarrhea cynomolgus monkeys and revealed the effector mechanisms. We demonstrated that FMT can mitigate the appearance of diarrheal symptoms and inhibit the increase in interleukin-6, interleukin-8, interleukin-1β, and interferon-γ and the decrease in interleukin-10 in serum. We confirmed that FMT restored the disturbance of gut bacteria by reducing the relative abundances of potential pathogens, including 5_2_54FAA, and 21_3, and increasing the levels of and CAG_367 in diarrheal monkeys. The metabolic pathways of healthy and FMT monkeys' gut bacteria were enriched in amino acid metabolism, carbohydrate metabolism, and lipid metabolism, while the metabolic pathways of pre-FMT monkeys' gut bacteria were enriched in antibiotic production. Moreover, a higher Ascomycota/Basidiomycota ratio, higher levels, and lower abundance were present in intestinal fungi after FMT. Although the abundance of the Archaea did not change significantly, it was inversely correlated with the anti-inflammatory factor IL-4 after FMT. These results support the further development and application of FMT for chronic diarrhea.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775123PMC
http://dx.doi.org/10.3390/biomedicines10123016DOI Listing

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