The immunomodulatory effect of lactulose on Enterococcus faecium fed preruminant calves.

Prebiotics and probiotics could represent an effective alternative to the use of synthetic antibiotics in nutrition. The mechanisms by which prebiotics affect the immune system have not yet been investigated in detail. Most effects have been attributed to increases in the innate and acquired immune responses. This study was conducted to elucidate the long-term effects of orally administered lactulose on the immune response in the intestinal tract of probiotic-fed calves. Preruminant calves were randomized to 3 feeding groups: milk replacer containing 1) no lactulose, 2) 1% lactulose, or 3) 3% lactulose. All 3 milk replacers contained 10(9) cfu Enterococcus faecium/kg. Messenger RNA expression of different cell activation markers, pro- and antiinflammatory cytokines, and IgA Fc receptor was investigated in the ileum, mesenterial lymph node, spleen, and white blood cells. A significantly greater number of blood lymphocytes were detected in the 3% lactulose group (P = 0.02) than in the control group. The expression results in male calves indicated that the transcription of IgA Fc receptor in the ileal mucosa of the 1% lactulose treatment group increased significantly (P = 0.04) and also tended to increase in the 3% lactulose group (P = 0.07). Furthermore, decreases in IL-10 and interferon-gamma mRNA expression were observed in the ileum (P = 0.04). The CD4-presenting lymphocytes were decreased significantly in the ileum (P = 0.04) and mesenteric lymph node (P = 0.01), whereas CD8-presenting lymphocytes were increased in the blood (P = 0.03) of females. Other proinflammatory cytokines (IL-1beta, IL-8, and tumor necrosis factor-alpha) and antiinflammatory cytokines (transforming growth factor-beta1) did not show significant differences in mRNA expression among treatment groups. The results indicate that additional lactulose feeding had an immunomodulatory effect on the composition of T-cell subsets in different immune compartments and had minor effects on pro- and antiinflammatory cytokine mRNA expression.

[1]  M. Pfaffl,et al.  Effect of lactulose on growth performance and intestinal morphology of pre-ruminant calves using a milk replacer containing Enterococcus faecium. , 2007, Animal : an international journal of animal bioscience.

[2]  G. Macfarlane,et al.  Review article: prebiotics in the gastrointestinal tract , 2006, Alimentary pharmacology & therapeutics.

[3]  D. Roth-Maier,et al.  Influence of pre-, pro-, and synbiotics on the intestinal availability of different B-vitamins , 2006, Archives of animal nutrition.

[4]  Michael W Pfaffl,et al.  RNA integrity and the effect on the real-time qRT-PCR performance. , 2006, Molecular aspects of medicine.

[5]  J. Novak,et al.  Probiotics and prebiotics for gastrointestinal infections , 2006, Current infectious disease reports.

[6]  H. Morton IgA Fc receptors in cattle and horses. , 2005, Veterinary immunology and immunopathology.

[7]  N. Antille,et al.  Enterococcus faecium SF68 enhances the immune response to Giardia intestinalis in mice. , 2005, The Journal of nutrition.

[8]  B. Watzl,et al.  Inulin, oligofructose and immunomodulation , 2005, British Journal of Nutrition.

[9]  J. Woof,et al.  Characterization of the Ligand Binding Site of the Bovine IgA Fc Receptor (bFcαR)* , 2004, Journal of Biological Chemistry.

[10]  D. Podolsky,et al.  Functional modulation of enterocytes by gram-positive and gram-negative microorganisms. , 2004, American journal of physiology. Gastrointestinal and liver physiology.

[11]  Qin Ouyang,et al.  Probiotics inhibit TNF-alpha-induced interleukin-8 secretion of HT29 cells. , 2004, World journal of gastroenterology.

[12]  G. Rechkemmer,et al.  Prebiotic inulin enriched with oligofructose in combination with the probiotics Lactobacillus rhamnosus and Bifidobacterium lactis modulates intestinal immune functions in rats. , 2004, The Journal of nutrition.

[13]  Teiji Kimura,et al.  Dietary Fructooligosaccharides Induce Immunoregulation of Intestinal IgA Secretion by Murine Peyer's Patch Cells , 2003, Bioscience, biotechnology, and biochemistry.

[14]  Tasuku Honjo,et al.  Intestinal IgA synthesis: regulation of front-line body defences , 2003, Nature Reviews Immunology.

[15]  G. Gibson,et al.  Probiotics as modulators of the gut flora , 2002, British Journal of Nutrition.

[16]  C. Field,et al.  The immune-enhancing effects of dietary fibres and prebiotics , 2002, British Journal of Nutrition.

[17]  J. Fulton,et al.  Lactulose may help prevent urinary tract infections , 2001, BMJ : British Medical Journal.

[18]  M. Pfaffl,et al.  A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.

[19]  S. Salminen,et al.  Probiotics: effects on immunity. , 2001, The American journal of clinical nutrition.

[20]  N. Cohen,et al.  Effects of dietary fructooligosaccharide on selected bacterial populations in feces of dogs. , 2000, American journal of veterinary research.

[21]  H. Hammon,et al.  Fructo-oligosaccharide supplementation: effects on metabolic, endocrine and hematological traits in veal calves. , 2000, Journal of veterinary medicine. A, Physiology, pathology, clinical medicine.

[22]  W. Hammes,et al.  Activation of Human Peripheral Blood Mononuclear Cells by Nonpathogenic Bacteria In Vitro: Evidence of NK Cells as Primary Targets , 2000, Infection and Immunity.

[23]  M. McBurney,et al.  The fermentable fiber content of the diet alters the function and composition of canine gut associated lymphoid tissue. , 1999, Veterinary immunology and immunopathology.

[24]  Y. Kanke,et al.  Secretion and excretion of immunoglobulin A to cecum and feces differ with type of indigestible saccharides. , 1999, Journal of nutritional science and vitaminology.

[25]  R. Wilson,et al.  T-cell subsets in blood and lymphoid tissues obtained from fetal calves, maturing calves, and adult bovine. , 1996, Veterinary immunology and immunopathology.

[26]  P. Marsden,et al.  Vascular endothelial platelet endothelial adhesion molecule-1 (PECAM-1) expression is decreased by TNF-alpha and IFN-gamma. Evidence for cytokine-induced destabilization of messenger ribonucleic acid transcripts in bovine endothelial cells. , 1996, Journal of immunology.

[27]  G R Gibson,et al.  Selective stimulation of bifidobacteria in the human colon by oligofructose and inulin. , 1995, Gastroenterology.

[28]  B. Diamond,et al.  Revisiting and revising suppressor T cells. , 1992, Immunology today.