Butyrate is a preferred energy source for colonic epithelial cells and is t
hought to play an important role in maintaining colonic health in humans. I
n order to investigate the diversity and stability of butyrate-producing or
ganisms of the colonic flora, anaerobic butyrate-producing bacteria were is
olated from freshly voided human fecal samples from three healthy individua
ls: an infant, an adult omnivore, and an adult vegetarian. A second isolati
on was performed on the same three individuals 1 year later. Of a total of
313 bacterial isolates, 74 produced more than 2 mM butyrate in vitro. Butyr
ate-producing isolates were grouped by 16S ribosomal DNA (rDNA) PCR-restric
tion fragment length polymorphism analysis. The results indicate very littl
e overlap between the predominant ribotypes of the three subjects; furtherm
ore, the flora of each individual changed significantly between the two iso
lations, Complete sequences of 16S rDNAs were determined fur 24 representat
ive strains and subjected to phylogenetic analysis, Eighty percent of the b
utyrate-producing isolates fell within the XIVa cluster of gram-positive ba
cteria as defined by M. D. Collins et at. (Int. J. Syst. Bacteriol. 44:812-
826, 1994) and A. Willems et al. (Int. J. Syst. Bacterial. 46:195-199, 1996
), with the most abundant group (10 of 24 or 42%) clustering with Eubacteri
um rectale, Eubacterium ramulus, and Roseburia cecicola, Fifty percent of t
he butyrate-producing isolates were net acetate consumers during growth, su
ggesting that they employ the butyryl coenzyme A-acetyl coenzyme A transfer
ase pathway for butyrate production, In contrast, only 1% of the 239 non-bu
tyrate-producing isolates consumed acetate.