Effect of intestinal microbiome in norm and pathology on human health
https://doi.org/10.21518/2079-701X-2017-1-155-159
Abstract
The intestinal microbiome plays a significant role in the regulation of peristalsis, exerts some influence on the functioning of the immune system, course of metabolic processes and formation of some aspects of behavior. There is evidence that maternal microflora can exert an influence on the fetus by translocation of bacteria or bacterial particles through the placental barrier, although, of course, the main colonization of the intestine of the infant occurs in the process of natural childbirth under the influence of the vaginal and intestinal flora of the mother. In children born by cesarean section the normal colonization of the gut is disturbed, which can determine a higher risk of developing in the future of some immune-mediated diseases, Type 1 diabetes mellitus and obesity. Medical men often try to adjust dysbiosis or changes in the composition of the fecal microflora called dysbiosis by the use of probiotics. In addition to the well-known effects of probiotics in the treatment of acute diarrhea in children, these drugs currently are being increasingly used for prevention of necrotizing enterocolitis of the newborn, despite the fact that evidence of the effectiveness of their routine use is not sufficient. A number of studies have shown that some probiotics may be effective in the prevention of atopic diseases, prevention and treatment of antibiotic-associated diarrhea, reducing the frequency and severity of necrotizing enterocolitis, relief of infant colic, and therapy of constipation. Given the role of microbiota in the development of obesity, some probiotics have been used and showed their effectiveness in weight loss. The fecal microflora transplantation was introduced relatively recently to treat Clostridium difficile infection and inflammatory bowel disease. In this review we discuss current data on the intestinal microbiota, its formation, functions, disturbance of the composition and possible ways of their correction.
About the Authors
Lifshitz LifshitzArgentina
MD
I. N. Zakharova
Russian Federation
MD, Prof.
Y. A. Dmitrieva
Russian Federation
PhD in medicine
References
1. Gorbach SL. Microbiology of the Gastrointestinal Tract. In: Baron S, editor. Medical Microbiology. 4th edition. Galveston (TX): University of Texas Medical Branch at Galveston, 1996. Chapter 95. Available from: http://www.ncbi.nlm.nih.gov/ books/NBK7670/.
2. Rautava S, Luoto R, Salminen S, et al .Microbial contact during pregnancy, intestinal colonization and human disease. Nat Rev Gastroenterol Hepatol, 2012, 9: 565-576.
3. Marques TM, Wall R, Ross RP et al. Programming infant gut microbiota: influence of dietary and environmental factors. Curr Opin Biotechnol, 2010, 21: 149-156.
4. Weng M, Walker WA.: The role of gut microbiota in programming the immune phenotype. J Dev Orig Health Dis, 2013, 4: 203-214.
5. Spiekermann G, Walker WA. Oral tolerance and its role in clinical disease. J Pediatr Gastroenterol Nutr, 2001, 32: 237-255.
6. Sudo N, Sawamura SA, Tanaka LA, et al. The requirement of intestinal flora for the development of an IgE production system fully susceptible to oral tolerance induction. J Immunol, 1997, 159: 1739-1745.
7. Karlsson MR, Kahu H, Hanson LA et al. Neonatal colonization of rats induces immunological tolerance to bacterial antigens. Eur J Immunol, 1999, 29: 109-118.
8. Neish AS. Microbes in gastrointestinal health and disease. Gastroenterology, 2009, 136: 65-80.
9. Rakoff-Nahoum S, Paglino J, Eslami-Varzaneh F et al. Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis. Cell, 2004, 118: 229-241.
10. Jimenez E, Fernandez L, Marin ML et al. Isolation of commensal bacteria from umbilical cord blood of healthy neonates born by cesarean section. Curr Microbiol, 2005, 51: 270-274.
11. Perez PF, Dore J, Leclerc M et al. Bacterial imprinting of the neonatal immune system: lessons from maternal cells? Pediatrics, 2007, 119: 724-732.
12. Satokari R, Gronroos T, Laitinen K et al. Bifidobacterium and Lactobacillus DNA in the human placenta. Lett Appl Microbiol, 2009, 48: 8-12.
13. Rautava S, Collado MC, Salminen S et al. Probiotics modulate host-microbe interaction in the placenta and fetal gut: a randomized, double-blind, placebo-controlled trial. Neonatology, 2012, 102: 178-184.
14. Grönlund MM, Lehtonen OP, Eerola E et al. Fecal microflora in healthy infants born by different methods of delivery: permanent changes in intestinal flora after Caesarean section delivery. J Pediatr Gastroenterol Nutr, 1999, 28: 19-25.
15. Eggesbø M, Botten G, Stigum H et al. Is delivery by cesarean section a risk factor for food allergy? J Allergy Clin Immunol, 2003, 112: 420-426.
16. Jost T, Lacroix C, Braegger CP, et al. New insights in gut microbiota establishment in healthy breast fed neonates. PLoS One, 2012, 7: e44595.
17. Rautava S, Luoto R, Salminen S et al. Microbial contact during pregnancy, intestinal colonization and human disease. Nat Rev Gastroenterol Hepatol, 2012, 9: 565-576.
18. Gueimonde M, Laitinen K, Salminen S et al. Breast-milk: a source of bifidobacteria for infant gut development and maturation? Neonatology, 2007, 92: 64-66.
19. Jost T, Lacroix C, Braegger C et al. Assessment of bacterial diversity in breastmilk using culture-dependent and culture independent approaches. Br J Nutr, 2013, 110: 1253-62.
20. Sjögren YM, Tomicic S, Lundberg A et al. Influence of early gut microbiota on the maturation of childhood mucosal and systemic immune responses. Clin Exp Allerg,. 2009, 39: 1842-1851.
21. Jost T, Lacroix C, Braegger C et al. Molecular monitoring of succession of bacterial communities in human neonates. Appl Environ Microbiol, 2002, 68: 219-226.
22. Roger LC, Costabile A, Holland DT et al. Examination of faecal Bifidobacterium populations in breast- and formula-fed infants during the first 18 months of life. Microbiology, 2010, 156: 3329-3341.
23. Marra F, Marra CA, Richardson K et al. Antibiotic use in children is associated with increased risk of asthma. Pediatrics, 2009, 123: 1003-1010.
24. Kronman MP, Zaoutis TE, Haynes K et al. Antibiotic exposure and IBD development among children: a population based cohort study. Pediatrics, 2012, 130: 794-703.
25. Cabrera-Rubio R, Collado MC, Laitinen K et al. The human milk microbiome changes over lactation and is shaped by maternal weight and mode of delivery. Am J Clin Nutr, 2012, 96: 544-551.
26. Backhed F, Ding H, Wang T et al. The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci USA, 2004, 101: 15718-15723.
27. Backhed F, Manchester JK, Semenkovich CF et al. Mechanisms underlying the resistance to diet-induced obesity in germ-free mice. Proc Natl Acad Sci USA, 2007, 104: 979-984.
28. Schwiertz A, Taras D, Schafer S et al: Microbiota and SCFA in lean and overweight healthy subjects. Epidemiology, 2009, 18: 190-195.
29. Velagapudi VR, Hezaveh R, Reigstad CS et al: The gut microbiota modulates host energy and lipid metabolism in mice. J Lipid Res, 2010, 51: 1101-1112.
30. Collado MC, Laitinen K, Salminen S, et al. Maternal weight and excessive weight gain during pregnancy modify the immunomodulatory potential of breast milk. Pediatr Res, 2012, 72: 77-85.
31. Kadooka Y, Sato M, Imaizumi K, et al. Regulation of abdominal adiposity by probiotics (Lactobacillus gasseri SBT2055) in adults with obese tendencies in a randomized controlled trial. Eur J Clin Nutr, 2010, 64: 636-643.
32. Sanchez M, Darimont C, Drapeau V et al. Effect of Lactobacillus rhamnosus CGMCC1.3724 supplementation on weight loss and maintenance in obese men and women. Br J Nutr, 2014, 111: 1507-19.
33. Miller AR, Barr RG, Eaton WO. Crying and motor behavior of six-week-old infants and postpartum maternal mood. Pediatrics, 1993, 92: 551-558.
34. Akman I, Kuscu K, Ozdemir N et al. Mothers’ postpartum psychological adjustment and infantile colic. Arch Dis Child, 2006, 91: 417-419.
35. Savino F, Cordisco L, Tarasco V et al. Lactobacillus reuteri DSM 17938 in infantile colic: A randomized, double-blind, placebo-controlled trial. Pediatrics, 2010, 126: 526-33.
36. Szajewska H, Gyrczuk E, Horvath A. Lactobacillus reuteri DSM 17938 for the management of infantile colic in breastfed infants: A randomized, double-blind, placebo-controlled trial. J Pediat, 2013, 162: 257-262.
37. Pärtty A, Luoto R, Kalliomäki M et al. Effects of Early Prebiotic and Probiotic Supplementation on Development of Gut Microbiota and Fussing and Crying in Preterm Infants: A Randomized, Double-Blind, Placebo-Controlled Trial. J Pediatr, 2013: 1272-7.
38. Barbara G, Stanghellini V, Brandi G et al. Interactions between commensal bacteria and gut sensorimotor function in health and disease. Am J Gastroenterol, 2005, 100: 2560-2568.
39. Kamath PS, Phillips SF, Zinsmeister AR. Shortchain fatty acids stimulate ileal motility in humans. Gastroenterology, 1988, 95: 1496-1502.
40. Guandalini S, Magazzù G, Chiaro A et al. VSL#3 improves symptoms in children with irritable bowel syndrome: a multicenter, randomized, placebo-controlled, double-blind, crossover study. J Pediatr Gastroenterol Nutr, 2010, 51: 24-30.
41. Coccorullo P, Strisciuglio C, Martinelli M et al. Lactobacillus reuteri (DSM 17938) in infants with functional chronic constipation: a doubleblind, randomized, placebo-controlled study. J Pediatr, 2010, 157: 598-602.
42. Bu LN, Chang MW, Ni YH. Lactobacillus casei rhamnosus Lcr 35 in children with chronic constipation. Pediatr. Internat., 2007, 49: 485-490.
43. Bakken JS. Borody TB, Lawrence J et al. Treating Clostridium difficile Infection With Fecal Microbiota Transplantation. Clin Gastroenterol Hepatol,2011, 9: 1044-1049.
44. Mattila E, Uusitalo-Seppala R et al. Fecal transplantation, through colonoscopy, is effective therapy for recurrent Clostridium difficile infection. Gastroenterology, 2012, 142: 490-496.
45. Reviewed in Tilg H, Kaser A. Gut microbiome, obesity, and metabolic dysfunction. J Clin Invest, 2011, 121: 2126-2132.
46. Gough E, Shaikh H, Manges AR. Systematic review of intestinal microbiota transplantation (fecal bacteriotherapy) for recurrent Clostridium difficile infection. Clin Infect Dis, 2011, 53: 994-1002.
47. van Nood E, Vrieze A, Nieuwdorp M et al. Duodenal infusion of donor feces for recurrent Clostridium difficile. N Engl J Med, 2013, 368: 407-15.
48. Kunde S, Pham A, Bonczyk S et al. Safety, tolerability, and clinical response after fecal transplantation in children and young adults with ulcerative colitis. J Pediatr Gastroenterol Nutr, 2013, 56: 597-601.
49. Russell GH, Kaplan JL, Youngster I, et al. Fecal Transplant for Recurrent Clostridium difficile Infection in Children With and Without Inflammatory Bowel Disease. J Pediatr Gastroenterol Nutr, 2014, 58: 588-592.
Review
For citations:
Lifshitz L, Zakharova IN, Dmitrieva YA. Effect of intestinal microbiome in norm and pathology on human health. Meditsinskiy sovet = Medical Council. 2017;(1):155-159. (In Russ.) https://doi.org/10.21518/2079-701X-2017-1-155-159