Selectively purified firmicutes spores from healthy human donors |
CDI |
Exact mechanism undefined. Possibly involves competitive exclusion of C. difficile presumably through secondary BA production (given the presence of firmicutes phyla) |
Approved for human use (trade name VOWST) |
Sims et al. (2023)
|
Microbiota suspension from healthy human donors |
CDI |
Competitive exclusion of C. difficile through an undefined mechanism |
Approved for human use (trade name Rebyota) |
Adolfsen et al. (2021)
|
Defined consortium of 33 gut commensals |
CDI |
Competitive exclusion of C. difficile through an unknown mechanism |
Human clinical trial (NCT01372943) |
Petrof et al. (2013)
|
Defined consortium of 11 gut commensals |
Tumor, infection (immunomodulation) |
Bacterial colonization, and bacterial antigen-mediated induction of interferon-γ-secretory CD8 T cells in colonic epithelial cells |
Mouse |
Tanoue et al. (2019)
|
C. scindens and engineered Bacteroides species (B. thetaiotaomicron, B. fragilis, or B. ovatus) |
Immunomodulation |
Induction of CD4+ regulatory T cells Treg cells |
Mouse |
Campbell et al. (2020)
|
Two step synthesis of 3β-hydroxydeoxycholic acid production from cholic acid via (i) cleavage of the 7α-hydroxyl group in cholic acid by Clostridium scindens, followed by (ii) epimerization of 3α-hydroxyl group in deoxycholic acid by engineered Bacteroides expressing hydroxysteroid dehydrogenases of Ruminococcus gnavus origin |