Impact of bile salt adaptation of Lactobacillus delbrueckii subsp. lactis 200 on its interaction capacity with the gut

Research in Microbiology

Volumn 162, Issue 8, 2011, Pages 782-790

  Burns, Patricia ^a   Reinheimer, Jorge ^a   Vinderola, Gabriel ^a  

^a UNIVERSIDAD NACIONAL DEL LITORAL   (Argentina)

Author keywords

Adherence; Autoaggregation; Bile salts; Immune response; Intestine; Lactobacilli

Indexed keywords

BILE ACID; BILE SALT;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BACTERIAL STRAIN; CONTROLLED STUDY; ELECTRON MICROSCOPY; FEMALE; HYDROPHOBICITY; IMMUNE RESPONSE; IMMUNOMODULATION; IN VITRO STUDY; IN VIVO STUDY; INTESTINE; INTESTINE FLUID; LACTOBACILLUS DELBRUECKII; MOUSE; NONHUMAN; PRIORITY JOURNAL; SURFACE PROPERTY;

ADAPTATION, PHYSIOLOGICAL; ANIMALS; BILE ACIDS AND SALTS; CATTLE; FEMALE; INTESTINE, SMALL; LACTOBACILLUS DELBRUECKII; MICE; MICE, INBRED BALB C; MICROBIAL VIABILITY; MODELS, BIOLOGICAL; SWINE;

BOVINAE; LACTOBACILLUS DELBRUECKII SUBSP. LACTIS; MUS; SUS;

EID: 80053384051     PISSN: 09232508     EISSN: 17697123     Source Type: Journal    
DOI: 10.1016/j.resmic.2011.07.005     Document Type: Article

References (37)

1. Basson A., Flemming L.A., Chenia H.Y. Evaluation of adherence, hydrophobicity, aggregation, and biofilm development of Flavobacterium johnsoniae-like isolates. Microb. Ecol. 2007, 55:1-14.
2. Begley M., Gahan C.G.M., Hill C. The interaction between bacteria and bile. FEMS Microbiol. Rev. 2005, 29:625-651.
3. Bibiloni R., Pérez P.F., De Antoni G.L. Will a high adhering capacity in a probiotic strain guarantee exclusion of pathogens from intestinal epithelia?. Anaerobe 1999, 5:519-524.
4. Burns P., Vinderola G., Binetti A., Quiberoni A., de los Reyes-Gavilán C., Reinheimer J. Bile-resistant derivatives obtained from non-intestinal dairy lactobacilli. Int. Dairy J. 2008, 18:377-385.
5. Burns P., Sánchez B., Vinderola G., Ruas-Madiedo P., Ruiz L., Margolles A., Reinheimer J., de los Reyes-Gavilán C. Inside the adaptation process of Lactobacillus delbrueckii subsp. lactis to bile. Int. J. Food Microbiol. 2010, 142:132-141.
6. Cesena C., Morelli L., Alander M., Siljander T., Tuomola E., Salminen S., Mattila-Sandholm T., Vilpponen-Salmela T., von Wright A. Lactobacillus crispatus and its nonaggregating mutant in human colonization trials. J. Dairy Sci. 2001, 84:1001-1010.
7. Collado M.C., Sanz Y. Induction of acid resistance in Bifidobacterium: a mechanism for improving desirable traits of potentially probiotic strains. J. Appl. Microbiol. 2007, 103:1147-1157.
8. de Moreno de Leblanc A., Perdigón G. Yogurt feeding inhibits promotion and progression of experimental colorectal cancer. Med. Sci. Monit. 2004, 10:96-104.
9. Dogi C.A., Perdigón G. Importance of the host specificity in the selection of probiotic bacteria. J. Dairy Res. 2006, 73:357-366.
10. FAO/WHO, 2002. Guidelines for the evaluation of probiotics in food. Food and Agriculture Organization of the United Nations and World Health Organization Working Group Report. http://www.fao.org/es/ESN/food/foodandfood_probio_en.stm.
11. Fuller R. Probiotics in human medicine. Gut 1991, 32:439-442.
12. Goldin B.R. Health benefits of probiotics. Br. J. Nutr. 1998, 80:203-207.
13. Golowczyc M.A., Mobili P., Garrote G.L., Abraham A.G., De Antoni G.L. Protective action of Lactobacillus kefir carrying S-layer protein against Salmonella enterica serovar Enteritidis. Int. J. Food Microbiol. 2007, 118:264-273.
14. Gopal P.K., Prasad J., Smart J., Gill H.S. In vitro adherence properties of Lactobacillus rhamnosus DR20 and Bifidobacterium lactis DR10 strains and their antagonistic activity against an enterotoxigenic Escherichia coli. Int. J. Food Microbiol. 2001, 67:207-216.
15. Guarner F., Perdigón G., Corthier G., Salminen S., Koletzko B., Morelli L. Should yoghurt cultures be considered probiotic?. Br. J. Nutr. 2005, 93:783-786.
16. Gueimonde M., Noriega L., Margolles A., de los Reyes-Gavilán C., Salminen S. Ability of Bifidobacterium strains with acquired resistance to bile to adhere to human intestinal mucus. Int. J. Food Microbiol. 2005, 101:341-346.
17. Haller D., Colbus H., Ganzle M.G., Scherenbacher P., Bode C., Hammes W.P. Metabolic and functional properties of lactic acid bacteria in the gastro-intestinal ecosystem: a comparative in vitro study between bacteria of intestinal and fermented food origin. Syst. Appl. Microbiol. 2001, 24:218-226.
18. Kotzamanidis C., Kourelis A., Litopoulou-Tzanetaki E., Tzanetakis N., Yiangou M. Evaluation of adhesion capacity, cell surface traits and immunomodulatory activity of presumptive probiotic Lactobacillus strains. Int. J. Food Microbiol. 2010, 140:154-163.
19. Lee N., Yun C., Kim S.W., Chang H., Kang C.W., Paik H.D. Screening of lactobacilli derived from chicken feces and partial characterization of Lactobacillus acidophilus A12 as animal probiotics. J. Microbiol. Biotechnol. 2008, 18:338-342.
20. Leverrier P., Dimova D., Pichereau V., Auffray Y., Boyaval P., Jan G. Susceptibility and adaptive response to bile salts in Propionibacterium freudenreichii: physiological and proteomic analysis. Appl. Environ. Microbiol. 2003, 69:3809-3818.
21. Meydani S.N., Ha W.K. Immunologic effects of yogurt. Am. J. Clin. Nutr. 2000, 71:861-872.
22. Oh S., Kim H., Worobo R.W. Characterization and purification of a bacteriocin produced by a potential probiotic culture, Lactobacillus acidophilus 30SC. J. Dairy Sci. 2000, 83:2747-2752.
23. Perdigón G., de Macias M.E., Alvarez S., Oliver G., de Ruiz Holgado A.P. Effect of perorally administered lactobacilli on macrophage activation in mice. Infect. Immun. 1986, 53:404-410.
24. Perdigón G., de Macias M.E., Alvarez S., Oliver G., de Ruiz Holgado A.P. Systemic augmentation of the immune response in mice by feeding fermented milks with Lactobacillus casei and Lactobacillus acidophilus. Immunology 1988, 63:17-23.
25. Perdigón G., Vintiñi E., Alvarez S., Medina M., Medici M. Study of the possible mechanisms involved in the mucosal immune system activation by lactic acid bacteria. J. Dairy Sci. 1999, 82:1108-1114.
26. Perdigón G., Medina M., Vintini E., Valdez J.C. Intestinal pathway of internalisation of lactic acid bacteria and gut mucosal immunostimulation. Int. J. Immunopathol. Pharmacol. 2000, 13:141-150.
27. Perdigón G., Fuller R., Raya R. Lactic acid bacteria and their effect on the immune system. Curr. Issues Intest. Microbiol. 2001, 2:27-42.
28. Siciliano R., Cacace G., Mazzeo M.F., Morelli L., Elli M., Rossi M., Malorni A. Proteomic investigation of the aggregation phenomenon in Lactobacillus crispatus. Biochim. Biophys. Acta 2008, 1784:335-342.
29. Skurnik D., Merighi M., Grout M., Gadjeva M., Maira-Litran T., Ericsson M., Goldmann D.A., Huang S.S., Datta R., Lee J.C., Pier G.B. Animal and human antibodies to distinct Staphylococcus aureus antigens mutually neutralize opsonic killing and protection in mice. J. Clin. Invest. 2010, 120:3220-3233.
30. Taranto M.P., de Ruiz Holgado A.P., de Valdez G.F. Bile salt hydrolase activity in Enterococcus faecium strains. Microbiol. Alim. Nutr. 1995, 13:375-379.
31. Taranto M.P., Perez-Martinez G., Font de Valdez G. Effect of bile acid on the cell membrane functionality of lactic acid bacteria for oral administration. Res. Microbiol. 2006, 157:720-725.
32. Tejada-Simon M.V., Lee J.H., Ustunol Z., Pestka J.J. Ingestion of yogurt containing Lactobacillus acidophilus and Bifidobacterium to potentiate immunoglobulin A responses to cholera toxin in mice. J. Dairy Sci. 1999, 82:649-660.
33. Valdez G.F., Martos G., Taranto M.P., Lorca G.L., Oliver G., Ruiz Holgado A.P. Influence of bile on β-galactosidase activity and cell viability of Lactobacillus reuteri when subjected to freeze-drying. J. Dairy Sci. 1996, 80:1955-1958.
34. Vinderola C.G., Medici M., Perdigón G. Relationship between interaction sites in the gut, hydrophobicity, mucosal immunomodulating capacities and cell wall protein profiles in indigenous and exogenous bacteria. J. Appl. Microbiol. 2004, 96:230-243.
35. Vinderola C.G., Duarte J., Thangavel D., Perdigón G., Farnworth E., Matar C. Immunomodulating capacity of kefir. J. Dairy Res. 2005, 72:195-202.
36. Vinderola G., Briggiler Marcó M., Guglielmotti D.M., Perdigón G., Giraffa G., Reinheimer J., Quiberoni A. Phage resistant mutants of Lactobacillus delbrueckii may have functional properties that differ from those of parent strains. Int. J. Food Microbiol. 2007, 116:96-102.
37. Voltan S., Castagliuolo I., Elli M., Longo S., Brun P., D'Incà R., Porzionato A., Macchi V., Palù G., Sturniolo G.C., Morelli L., Martines D. Aggregating phenotype in Lactobacillus crispatus determines intestinal colonization and TLR2 and TLR4 modulation in murine colonic mucosa. Clin. Vaccine Immunol. 2007, 14:1138-1148.