Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-27T13:38:40.045Z Has data issue: false hasContentIssue false

Modulation of gut mucosal biofilms

Published online by Cambridge University Press:  08 March 2007

Brigitta Kleessen*
Affiliation:
Veterinary Faculty, Institute of Bacteriology and Mycology, University of Leipzig, An den Tierkliniken 29, D-04103, Leipzig, Germany
Michael Blaut
Affiliation:
German Institute of Human Nutrition (DIFE) Potsdam-Rehbrücke, D-14558 Nuthetal, Germany
*
*Corresponding author: Dr Brigitta Kleessen, fax +49 341 9 73 81 97, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Non-digestible inulin-type fructans, such as oligofructose and high-molecular-weight inulin, have been shown to have the ability to alter the intestinal microbiota composition in such a way that members of the microbial community, generally considered as health-promoting, are stimulated. Bifidobacteria and lactobacilli are the most frequently targeted organisms. Less information exists on effects of inulin-type fructans on the composition, metabolism and healthrelated significance of bacteria at or near the mucosa surface or in the mucus layer forming mucosa-associated biofilms. Using rats inoculated with a human faecal flora as an experimental model we have found that inulin-type fructans in the diet modulated the gut microbiota by stimulation of mucosa-associated bifidobacteria as well as by partial reduction of pathogenic Salmonella enterica subsp. enterica serovar Typhimurium and thereby benefit health. In addition to changes in mucosal biofilms, inulin-type fructans also induced changes in the colonic mucosa stimulating proliferation in the crypts, increasing the release of mucins, and altering the profile of mucin components in the goblet cells and epithelial mucus layer. These results indicate that inulin-type fructans may stabilise the gut mucosal barrier. Dietary supplementation with these prebiotics could offer a new approach to supporting the barrier function of the mucosa.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2005

References

Amann, R & Kühl, M (1998) In situ methods for assessment of microorganisms and their activities. Curr Opin Microbiol 1, 352358.Google Scholar
Amann, RI, Krumholz, L & Stahl, DA (1990) Fluorescent-oligonucleotide probing of whole cells for determinative phylogenetic, and environmental studies in microbiology. J Bacteriol 172, 762770.CrossRefGoogle ScholarPubMed
Amann, RI, Ludwig, W & Schleifer, K-H (1995) Phylogenetic identification and in situ detection of individual microbial cells without cultivation. Microbiol Rev 59, 143169.CrossRefGoogle ScholarPubMed
Berg, RD (1996) The indigenous gastrointestinal microflora. Trends Microbiol 4, 430435.Google Scholar
Bouhnik, Y, Vahedi, K, Achour, L, et al. (1999) Short-chain fructo-oligosaccharide administration dose-dependently increases fecal bifidobacteria in healthy humans. J Nutr 129, 113116.CrossRefGoogle ScholarPubMed
Campbell, JM, Fahey, GC & Bryan, WW (1997) Selected indigestible oligosaccharides affect large bowel mass, cecal and fecal short-chain fatty acids, pH and microflora in rats. J Nutr 127, 130136.Google Scholar
Cummings, JH & Macfarlane, GT (1997) Colonic microflora: nutrition and health. Nutrition 13, 476478.Google Scholar
Deplancke, B & Gaskins, HR (2001) Microbial modulation of innate defense: goblet cells and the intestinal mucus layer. Am J Clin Nutr 73, Suppl., 1131S1141S.Google Scholar
Djouzi, Z & Andrieux, C (1997) Compared effects of three oligosaccharides on metabolism of intestinal microflora in rats inoculated with a human faecal flora. Br J Nutr 78, 313324.Google Scholar
Fontaine, N, Meslin, JC, Lory, S & Andrieux, C (1996) Intestinal mucin distribution in the germ-free rat and in the heteroxenic rat habouring a human bacterial flora: effect of inulin in the diet. Br J Nutr 75, 881892.Google Scholar
Forstner, JF (1978) Intestinal mucins in health and disease. Digestion 17, 234263.Google Scholar
Franks, AH, Harmsen, HJM, Raangs, GC, Jansen, GJ, Shut, F & Welling, GW (1998) Variation of bacterial populations in human feces measured by fluorescent in situ hybridization with group-specific 16S rRNA-targeted oligonucleotide probes. Appl Environ Microbiol 64, 33363345.Google Scholar
Freitas, M & Cayuela, C (2000) Microbial modulation of host intestinal glycosylation patterns. MEHD 12, Suppl. 2, 165178.Google Scholar
Fuller, R & Gibson, GR (1997) Modification of the intestinal microflora using probiotics and prebiotics. Scand J Gastroenterol 32, Suppl. 222, 2831.Google Scholar
Gibson, GR, Beatty, EB, Wang, X & Cummings, JH (1995) Selective stimulation of bifidobacteria in the human colon by oligofructose and inulin. Gastroenterology 108, 975982.Google Scholar
Hooper, LV & Gordon, JI (2001) Commensal host–bacterial relationships in the gut. Science 292, 11151118.Google Scholar
Kleessen, B, Sykura, B, Zunft, H-J & Blaut, M (1997) Effects of inulin and lactose on fecal microflora, microbial activity, and bowel habit in elderly constipated persons. Am J Clin Nutr 65, 13971402.Google Scholar
Kleessen, B, Hartmann, L & Blaut, M (2001) Oligofructose and long-chain inulin: influence on the gut microbial ecology of rats associated with a human faecal flora. Br J Nutr 86, 291300.Google Scholar
Kleessen, B, Kroesen, AJ, Buhr, HJ & Blaut, M (2002) Mucosal and invading bacteria in patients with inflammatory bowel disease compared with controls. Scand J Gastroenterol 37, 10341041.CrossRefGoogle ScholarPubMed
Kleessen, B, Hartmann, L & Blaut, M (2003) Fructans in the diet cause alterations of intestinal mucosal architecture, released mucins and mucosa-associated bifidobacteria in gnotobiotic rats. Br J Nutr 89, 597606.Google Scholar
Kruse, H-P, Kleessen, B & Blaut, M (1999) Effects of inulin on faecal bifidobacteria in human subjects. Br J Nutr 82, 375382.CrossRefGoogle ScholarPubMed
Le Blay, G, Michel, C, Blottiere, HM & Cherbut, C (1999) Prolonged intake of fructo-oligosaccharides induces a short-term elevation of lactic acid-producing bacteria and a persistent increase in cecal butyrate in rats. J Nutr 129, 22312235.CrossRefGoogle Scholar
Lu, L & Walker, WA (2001) Pathologic and physiologic interactions of bacteria with the gastrointestinal epithelium. Am J Clin Nutr 73, Suppl., 1124S1130S.Google Scholar
Macfarlane, S, McBain, AJ & Macfarlane, GT (1997) Consequences of biofilms and sessile growth in the large intestine. Adv Dent Res 11, 5968.CrossRefGoogle ScholarPubMed
Macfarlane, S, Cummings, JH & Macfarlane, GT (1999) Bacterial colonisation of surfaces in the large intestine. In Colonic Microbiota, Nutrition and Health, pp. 7187 [Gibson, GR, Roberfroid, MB, editors]. Netherlands: Kluwer Academic Publisher.CrossRefGoogle Scholar
Neish, AS (2002) The gut microflora and intestinal epithelial cells: a continuing dialogue. Microbes Infect 4, 309317.CrossRefGoogle ScholarPubMed
Pluske, JR, Tompson, MJ, Atwood, CS, Bird, PH, Williams, IH & Hartmann, PE (1996) Maintenance of villus height and crypt depth, and enhancement of disaccharide digestion and monosaccharide absorption, in piglets fed on cows' whole milk after weaning. Br J Nutr 76, 409422.Google Scholar
Pullan, RD, Thomas, GA, Rhodes, M, Newcombe, RG, Williams, GT, Allen, A & Rhodes, J (1994) Thickness of adherent mucus gel on colonic mucosa in humans and its relevance to colitis. Gut 35, 353359.Google Scholar
Rhodes, JM (1997) Mucins and inflammatory bowel disease. Q J Med 90, 7982.CrossRefGoogle ScholarPubMed
Romeis, R (1989) Polysaccharide and mucous substances. In Microscopic Technique, 439444 [Böck, P, editors]. Munich, Vienna, Baltimore: Urban & Schwarzenberg.Google Scholar
Sakata, T (1987) Stimulatory effect of short-chain fatty acids on epithelial cell proliferation in the rat intestine: a possible explanation for trophic effects on fermentable fibre, gut microbes and luminal trophic factors. Br J Nutr 58, 95103.CrossRefGoogle ScholarPubMed
Salminen, S, Isolauri, E & Onnela, T (1995) Gut flora in normal and disordered states. Chemotherapy 41, Suppl. I, 511.Google Scholar
Tolker-Nielsen, T & Molin, S (2000) Spatial organization of microbial biofilms communities. Microb Ecol 40, 7584.CrossRefGoogle Scholar