Monocolonization with Bacteroides ovatus protects immunodeficient SCID mice from mortality in chronic intestinal inflammation caused by long-lasting dextran sodium sulfate treatment

Physiological Research

Volumn 58, Issue 1, 2009, Pages 101-110

  Hudcovic, T ^a   Kozakova H ^a   Kolinska J ^b   Stepankova R ^a   Hrncir T ^a   Tlaskalova Hogenova H ^a  

^a INSTITUTE OF MICROBIOLOGY   (Czech Republic)

^b INSTITUTE OF PHYSIOLOGY   (Czech Republic)

Author keywords

Bacteroides ovatus; Dextran sulfate sodium colitis; Gnotobiotic mice; Ulcerative colitis

Indexed keywords

ALKALINE PHOSPHATASE; DEXTRAN SULFATE; GAMMA GLUTAMYLTRANSFERASE; LACTASE;

ANIMAL; ARTICLE; BACTEROIDES; BAGG ALBINO MOUSE; CHEMICALLY INDUCED DISORDER; CHRONIC DISEASE; COLITIS; COLON; DISEASE MODEL; ENZYMOLOGY; GROWTH, DEVELOPMENT AND AGING; HOSPITALIZATION; INTESTINE MUCOSA; JEJUNUM; METABOLISM; MICROBIOLOGY; MICROVILLUS; MOUSE; MOUSE MUTANT; PATHOLOGY; TIME;

ALKALINE PHOSPHATASE; ANIMALS; BACTEROIDES; CHRONIC DISEASE; COLITIS; COLON; DEXTRAN SULFATE; DISEASE MODELS, ANIMAL; GAMMA-GLUTAMYLTRANSFERASE; INTESTINAL MUCOSA; JEJUNUM; LACTASE; MICE; MICE, INBRED BALB C; MICE, SCID; MICROVILLI; SEVERITY OF ILLNESS INDEX; TIME FACTORS;

EID: 66549102005     PISSN: 08628408     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (40)

1. Arvanitakis C, Abnormalities of jejunal enzymes in ulcerative colitis and Crohn's disease. Digestion 19: 259-266, 1979.
2. +-cell depleted, athymic and NK-cell depleted SCID mice. Inflam Res 45: 181-191, 1996.
3. Cooper HS, Murthy SN, Shah RS, Sedergran DJ, Clinopathologic study of dextrane sulfate sodium experimental murine colitis. Lab Invest 69: 238-249, 1993.
4. Dahlqvist A, Method for assay of intestinal disaccharidases. Anal Biochem 7: 18-25, 1964.
5. Dieleman LA, Ridwan BU, Tennyson GS, Beagley KW, Bucy RP, Elson CO, Dextran sulfate sodiuminduced colitis occurs in severe combined immunodeficient mice. Gastroenterology 107: 1643-1652, 1994.
6. Ehrhart RO, Lúdvíksson BR, Gray B, Neurath M, Strober W, Induction and prevention of colonic inflammation in IL-2-deficient mice. J Immunol 158: 566-573, 1997.
7. Farkas S, Herfarth H, Rössle M, Schroeder J, Steinbauer M, Guba M, Beham A, Schölmerich J, Jauch KW, Anthuber M, Quantification of mucosal leukocyte endothelial cell interaction by in vivo fluorescence microscopy in experimental colitis in mice. Clin Exp Immunol 126: 250-258, 2001.
8. Guttman JA, Samji FN, Li Y, Vogl AW, Finlay BB, Evidence that tight junctions are disrupted due to intimate bacterial contact and not inflammation during attaching and effacing pathogen infection in vivo. Infect Immun 74: 6075-6084, 2006.
9. Harada T, Koyama I, Kasahara T, Alpers DH, Komoda T, Heat shock induces intestinal-type alkaline phosphatase in rat IEC-18 cells. Am J Physiol 284: G255-G262, 2003.
10. Hooper LV, Gordon JI, Commensal host-bacterial relationships in the gut. Science 292: 1115-1118, 2001.
11. Hooper LV, Bacterial contribution to mammalian gut development. Trends Microbiol 12: 129-134, 2004.
12. Hudcovic T, Štěpánková R, Cebra J, Tlaskalová-Hogenová H, The role of microflora in the development of intestinal inflammation: acute and chronic colitis induced by dextran sulfate in germ-free and conventionally reared immunocompetent and immunodeficient mice. Folia Microbiol 46: 565-572, 2001.
13. Hudcovic T, Štěpánková R, Kozáková H, Hrnčíř T, Tlaskalová-Hogenová H., Effects of monocolonization with Escherichia coli strains O6K13 and Nissle 1917 on the development of experimentally induced acute and chronic intestinal inflammation in germ-free immunocompetent and immunodeficient mice. Folia Microbiol 52: 618-626, 2007.
14. Kessler M, Acuto O, Storelli C, Murer H, Müller M, Semenza G, A modified procedure for the rapid preparation of efficiently transporting vesicles from small intestinal brush border membranes. Their use in investigating some properties of D-glucose and choline transport systems. Biochim Biophys Acta 506: 136-154, 1978.
15. Kitajima S, Morimoto M, Sagara E, Shimizu C, Ikeda Y, Dextran sulfate sodium-induced colitis in germ-free IQI/Jic mice. Exp Anim 50: 387-395, 2001.
16. Kitajima S, Morimoto M, Sagara E, Shimizu C, Ikeda Y, A model for dextran sulfate sodium (DSS)-induced colitis: bacterial degradation of DSS does not occur after incubation with mouse cecal contents. Exp Anim 51: 2003-206, 2002.
17. Kolínská J, Kraml J, Separation of sucrase-isomaltase and of glucoamylase of rat intestine. Biochim Biophys Acta 28: 235-247, 1972.
18. Kolínská J, Kraml J, Zákostelecká M, Kadlecová L, Actinomycin D suppresses hydrocortisone-induced changes in distribution and sialylation of brush-border enzymes in jejunal villi and crypts. Biochem Int 21: 581-591, 1990.
19. Kozáková H, Štěpánková R, Řeháková Z, Kolínská J, Differences in enterocyte brush border enzyme activities in ageing rats reared in germ-free and conventional conditions. Physiol Res 47: 253-258, 1998.
20. Kozáková H, Řeháková Z, Kolínská J, Bifidobacterium bifidum monoassociation of gnotobiotic mice: effect on enterocyte brush-border enzymes. Folia Microbiol 46: 573-576, 2001.
21. Kozáková H, Kolínská J, Lojda Z, Řeháková Z, Šinkora J, Zákostelecká M, Šplíchal I, Tlaskalová-Hogenová H, Effect of bacterial monoassociation on brush-border enzyme activities in ex-germ-free piglets: comparison of commensal and pathogenic Escherichia coli strains. Microbes Infect 8: 2629-2639, 2006.
22. Kraml J, Kolínská J, Ellederová D, Hiršová D, β-glucosidase (phlorizin hydrolase) activity of the lactase fraction isolated from the small intestinal mucosa of infant rats, and the relationship between β-glucosidases and β-galactosidases. Biochim Biophys Acta 258: 520-530, 1972.
23. Lowry OH, Rosenbrough WJ, Farr F, Randall RJ, Protein measurement with Folin phenol reagent. J Biol Chem 193: 265-275, 1951.
24. Lucke K, Miehlke S, Jacobs E, Schuppler M, Prevalence of Bacteroides and Prevotella spp. in ulcerative colitis. J Med Microbiol 55: 617-624, 2006.
25. Nagatsu T, Hino M, Fuyamaha H, Hayakawa T, Sakakibara S, Nakagawa Y, Takemoto T, New chromogenic substrates for X-prolyl dipeptidylaminopeptidase. Anal Biochem 74: 466-476, 1976.
26. Nieto N, Torres MI, Fernandez MI, Giron MD, Rios A, Suarez MD, Gil A, Experimental ulcerative colitis impairs antioxidant defense system in rat intestine. Dig Dis Sci 45: 1820-1827, 2000.
27. Okayasu I, Hatakeyama S, Yamada M, Ohkusa T, Inagi Y, Nakya R, A novel method in the induction of reliable experimental acute and chronic ulcerative colitis in mice. Gastroenterology 98: 694-702, 1990.
28. Poxton IR, Brown R, Sawyerr A, Ferguson A, Mucosa-associated bacterial flora of the human colon. J Med Microbiol 46: 85-91, 1997.
29. Rath HC, Wilson KH, Sartor RB, Differential induction of colitis and gastritis in HLA-B27 transgenic rats selectively colonized with Bacteriodes vulgatus or Escherichia coli. Infect Immun 67: 2969-2974, 1999.
30. Reyes BM, Danase S, Sans M, Fiocchi C, Levine AD, Redox equilibrium in mucosal T cells tunes the intestinal TCR signaling threshold. J Immunol 175: 2158-2166, 2005.
31. Saitoh S, Noda S, Aiba Z, Takagi A, Sakamoto M, Benno Z, Koga Z, Bacteroides ovatus as the predominant commensal intestinal microbe causing a systemic antibody response in inflammatory bowel disease. Clin Diagn Lab Immunol 9: 54-59, 2002.
32. Schultz M, Strauch UG, Linde HJ, Watzl S, Obermeier F, Gottl C, Dunger N, Grunwald N, Scholmerich J, Rath HC, Preventive effects of Escherichia coli strain Nissle 1917 on acute and chronic intestinal inflammation in two different murine models of colitis. Clin Diagn Lab Immunol 11: 372-378, 2004.
33. Sido B, Hack V, Hochlehnert, Lipps H, Herfarth C, Dröge W, Impairment of intestinal glutathione synthesis in patients with inflammatory bowel disease. Gut 42: 485-492, 1998.
34. Siegmund B, Fantuzzi G, Rieder F, Gamboni-Robertson F, Lehr HS, Hartmann G, Dinarello CA, Endres S, Eigler A, Neutralization of Interleukin-18 reduces severity in murine colitis and intestinal IFN-γ and TNF-α production. Am J Physiol 281: R1264-R1273, 2001.
35. Sivakumar PV, Westrich GM, Kanaly S, Garka K, Born TL, Derry JMJ, Viney JL, Interleukin 18 is a primary mediator of inflammation associated with dextran sulphate sodium induced colitis: blocking interleukin 18 attenuates intestinal damage. Gut 50: 812-820, 2002.
36. Sokol H, Seksik P, Rigottier-Gois L, Lay C, Lepage P, Podglajen I, Marteau P, Dore J, Specificities of the fecal microbiota in inflammatory bowel disease. Inflam Bowel Dis 12, 106-111, 2006.
37. Sydora BC, Tavernini MM, Doyle JG, Fedorak RN, Association with selected bacteria does not cause enterocolitis in IL-10 gene-deficient mice despite a systemic immune response. Dig Dis Sci 50, 905-913, 2005.
38. Štěpánková R, Rearing of germ-free rats, mice, and rabbits. In: Immunology Methods Manual Lefkovits I (ed), Gnotobiological Models Tlaskalová H, Šterzl J (eds), Academic Press, New York, 1997, pp 1537-1542.
39. Thompson GA, Meister A, Hydrolysis and transfer reactions catalyzed by gamma-glutamyl transpeptidase; evidence for separate substrate sites and for high affinity of L-cystine. Biochem Biophys Res Commun 71, 32-36, 1976.
40. Tlaskalová-Hogenová H, Tučková L, Štěpánková R, Hudcovic T, Palová-Jelínková L, Kozáková H, Rossmann P, Sanchéz D, Cinová J, Hrnčíř T, Kverka M, Frolová L, Uhlig H, Powrie F, Bland P, Involvement of innate immunity in the development of inflammatory and autoimmune diseases. Ann N Y Acad Sci 1051, 787-798, 2005.