Japan bThis study was performed to determine the effects of feeding a fiber-rich fraction of Brassica vegetables on the immune response through changes in enteric bacteria and short-chain fatty acid (SCFA) production in normal mice. The boiled-water-insoluble fraction of Brassica rapa L. (nozawana), which consists mainly of dietary fiber, was chosen as a test material. A total of 31 male C57BL/6J mice were divided into two groups and housed in a specific-pathogen-free facility. The animals were fed either a control diet or the control diet plus the insoluble B. rapa L. fraction for 2 weeks and sacrificed to determine microbiological and SCFA profiles in lower-gut samples and immunological molecules. rRNA-based quantification indicated that the relative population of Bacteroidetes was markedly lower in the colon samples of the insoluble B. rapa L. fraction-fed group than that in the controls. Populations of the Eubacterium rectale group and Faecalibacterium prausnitzii, both of which are representative butyrateproducing bacteria, doubled after 2 weeks of fraction intake, accompanying a marginal increase in the proportion of colonic butyrate. In addition, feeding with the fraction significantly increased levels of the anti-inflammatory cytokine interleukin-10 (IL-10) and tended to increase splenic regulatory T cell numbers but significantly reduced the population of cells expressing activation markers. We demonstrated that inclusion of the boiled-water-insoluble fraction of B. rapa L. can alter the composition of the gut microbiota to decrease the numbers of Bacteroidetes and to increase the numbers of butyrate-producing bacteria, either of which may be involved in the observed shift in the production of splenic IL-10.A nimals coexist with microbial symbionts that act as an integral component of the host's physiology in the gastrointestinal (GI) tract (1). The vast majority of GI bacteria are strict anaerobes that derive energy from fermentation, by which indigestible complex carbohydrates (cellulose, pectin, gums, beta-glucan, and lignin) are converted to short-chain fatty acids (SCFAs), such as acetate, propionate, and butyrate, as terminal electron acceptors (2-4). As each member of the GI microbiota has its own preferences for different energy sources (5, 6), the profile of dominant species in the human gut microbiota can potentially be modified by the types of dietary carbohydrate in the diet.Among the SCFAs, butyrate acts as a primarily effective molecule on physiological regulatory systems of the host gut and as an energy source for the colonic epithelium of the host. There has long been interest in the immunomodulatory and anti-inflammatory effects of butyrate on colonic epithelial cells (7-9). The production of butyrate in the GI tract is supported by specific groups of bacteria, i.e., butyrate producers, which are considered to play important roles in the maintenance of gut health (10, 11). The main human colonic butyrate producers belong to two groups of Gram-positive firmicutes: Faecalibacterium prausn...